The core responsibility of this position is to contribute to the production of a wide range of products and fluidic components for the aerospace industry. Specifically, the role focusses on supporting routine business operations related to the assembly, integration, and testing of space-certified products, including non-return valves, flow control valves, solenoid valves, cold gas thrusters, and upcoming development projects. Prior experience as a Mechanical Fitter or demonstrable practical engineering skills, preferably acquired through an apprenticeship or within an engineering-related organisation. Primary Duties Perform precise assembly and testing tasks. Conduct integrity assessments of assembled systems using high-pressure gases and specialised leak detection equipment, such as helium mass spectrometers. Prepare components for assembly and testing by employing automated particle counting equipment or patch sample counting techniques. Utilise digital voltmeters, oscilloscopes, data acquisition systems, and high-voltage dielectric and insulation resistance test equipment. Engage in material joining processes, including manual TIG (Tungsten Inert Gas) welding and orbital welding, while maintaining weld inspection records for parts and test pieces. Perform periodic maintenance of cleanroom facilities and testing equipment.
Apr 25, 2024
Full time
The core responsibility of this position is to contribute to the production of a wide range of products and fluidic components for the aerospace industry. Specifically, the role focusses on supporting routine business operations related to the assembly, integration, and testing of space-certified products, including non-return valves, flow control valves, solenoid valves, cold gas thrusters, and upcoming development projects. Prior experience as a Mechanical Fitter or demonstrable practical engineering skills, preferably acquired through an apprenticeship or within an engineering-related organisation. Primary Duties Perform precise assembly and testing tasks. Conduct integrity assessments of assembled systems using high-pressure gases and specialised leak detection equipment, such as helium mass spectrometers. Prepare components for assembly and testing by employing automated particle counting equipment or patch sample counting techniques. Utilise digital voltmeters, oscilloscopes, data acquisition systems, and high-voltage dielectric and insulation resistance test equipment. Engage in material joining processes, including manual TIG (Tungsten Inert Gas) welding and orbital welding, while maintaining weld inspection records for parts and test pieces. Perform periodic maintenance of cleanroom facilities and testing equipment.
Mechanical Fitter required to join a precision aerospace production team to work in a cleanroom environment on the assembly, integration and testing of aerospace devices. Our international Aerospace and Defence client is going through a continued period of expansion and looking for Precision Mechanical Assembly Technicians. The ideal candidate will have experience as a Mechanical fitter experience ideally through apprenticeship with exposure to and of the following; non return valves, flow control valves, solenoid valves, cold gas thrusters or any fluidic components for the space industry. Training and skills development will be provided, extended working hours may be required to meet production targets. Responsibilities Precision assembly and test activities in a Class 8 clean room. Testing the integrity of assembled systems using high pressure gases and leak detection equipment such as helium mass spectrometers. Cleaning components in preparation for assembly and test activities using automatic particle counting equipment and patch sample counting techniques. Electrical testing Gas flow testing of valves, thrusters and fluidic components to ensure components are within tolerance prior to assembly. Digital voltmeters, oscilloscopes, data acquisition systems, high voltage dielectric and insulation resistance test equipment. Material joining processes including manual TIG (Tungsten Inert Gas) welding, orbital welding, and compiling weld inspection reports on parts and test pieces.
Apr 24, 2024
Full time
Mechanical Fitter required to join a precision aerospace production team to work in a cleanroom environment on the assembly, integration and testing of aerospace devices. Our international Aerospace and Defence client is going through a continued period of expansion and looking for Precision Mechanical Assembly Technicians. The ideal candidate will have experience as a Mechanical fitter experience ideally through apprenticeship with exposure to and of the following; non return valves, flow control valves, solenoid valves, cold gas thrusters or any fluidic components for the space industry. Training and skills development will be provided, extended working hours may be required to meet production targets. Responsibilities Precision assembly and test activities in a Class 8 clean room. Testing the integrity of assembled systems using high pressure gases and leak detection equipment such as helium mass spectrometers. Cleaning components in preparation for assembly and test activities using automatic particle counting equipment and patch sample counting techniques. Electrical testing Gas flow testing of valves, thrusters and fluidic components to ensure components are within tolerance prior to assembly. Digital voltmeters, oscilloscopes, data acquisition systems, high voltage dielectric and insulation resistance test equipment. Material joining processes including manual TIG (Tungsten Inert Gas) welding, orbital welding, and compiling weld inspection reports on parts and test pieces.
The core responsibility of this position is to contribute to the production of a wide range of products and fluidic components for the aerospace industry. Specifically, the role focusses on supporting routine business operations related to the assembly, integration, and testing of space-certified products, including non-return valves, flow control valves, solenoid valves, cold gas thrusters, and upcoming development projects. Prior experience as a Mechanical Fitter or demonstrable practical engineering skills, preferably acquired through an apprenticeship or within an engineering-related organisation. Primary Duties Perform precise assembly and testing tasks. Conduct integrity assessments of assembled systems using high-pressure gases and specialised leak detection equipment, such as helium mass spectrometers. Prepare components for assembly and testing by employing automated particle counting equipment or patch sample counting techniques. Utilise digital voltmeters, oscilloscopes, data acquisition systems, and high-voltage dielectric and insulation resistance test equipment. Engage in material joining processes, including manual TIG (Tungsten Inert Gas) welding and orbital welding, while maintaining weld inspection records for parts and test pieces. Perform periodic maintenance of cleanroom facilities and testing equipment.
Apr 24, 2024
Full time
The core responsibility of this position is to contribute to the production of a wide range of products and fluidic components for the aerospace industry. Specifically, the role focusses on supporting routine business operations related to the assembly, integration, and testing of space-certified products, including non-return valves, flow control valves, solenoid valves, cold gas thrusters, and upcoming development projects. Prior experience as a Mechanical Fitter or demonstrable practical engineering skills, preferably acquired through an apprenticeship or within an engineering-related organisation. Primary Duties Perform precise assembly and testing tasks. Conduct integrity assessments of assembled systems using high-pressure gases and specialised leak detection equipment, such as helium mass spectrometers. Prepare components for assembly and testing by employing automated particle counting equipment or patch sample counting techniques. Utilise digital voltmeters, oscilloscopes, data acquisition systems, and high-voltage dielectric and insulation resistance test equipment. Engage in material joining processes, including manual TIG (Tungsten Inert Gas) welding and orbital welding, while maintaining weld inspection records for parts and test pieces. Perform periodic maintenance of cleanroom facilities and testing equipment.
Position: Plant Technician Commercial Boilers (High Temperature Hot Water) Location: Burghfield Role: Permanent Morson Talent is excited to present a fantastic opportunity for a Plant Operator to join a company that has received significant investment and operates on an impressive 225-acre site. Our client specialises in research and production activities for the Ministry of Defence, contributing to national defence and security efforts. As a Plant Technician, your primary responsibility will be to provide essential maintenance and support for all High-Temperature Hot Water (HTHW) operations. Role Responsibilities: • Monitor HTHW plant and associated equipment, conducting safety equipment tests • Capable of safely shutting down and securing any malfunctioning equipment that poses a safety risk, and promptly notifying relevant engineers for maintenance • Support the HTHW supervisor with planned, reactive, or project tasks while ensuring compliance with site procedures and safety protocols • Monitor, maintain, investigate, and address issues related to the site Building Management System (BMS) • Conduct regular plant checks, report any defects, and ensure cleanliness, tidiness, and safety in all HTHW plant rooms • Identify and report defects to the HTHW supervisor promptly • Provide efficient responses to customer inquiries and helpdesk requests • Ensure compliance with regulations and escalate any safety or security concerns to the appropriate authorities • Offer innovative solutions and suggestions to enhance processes, building infrastructure, plant, and systems • Cultivate collaborative relationships with end-users Skills and Qualifications: • Technical expertise, qualifications, or apprenticeship in High-Temperature Hot Water (HTHW) operations is essential • BOAS 9.2 certification • Familiarity with BG02 guidance on safe operation of hot water boilers • Knowledge of INDG436 guidelines for the safe management of industrial steam and hot water boilers • Understanding of PSSR regulations 2000 L122 ACOP • Proficiency in BMS systems • Experience with key operational procedures such as time sheets, planned maintenance systems, quality assurance, and health & safety protocols • Proven ability to effectively resolve customer issues within specific contracts • Smart and well-presented appearance • All candidates must undergo DV Clearance If you meet the requirements listed above and are eager to contribute to a vital role within a dynamic and forward-thinking organization, we encourage you to apply for this exciting opportunity. Please submit your application with a detailed CV showcasing your relevant experience and qualifications. We look forward to welcoming a talented and dedicated Plant Technician to our team. Morson Talent is an equal opportunities employer. JBRP1_UKTJ
Apr 24, 2024
Full time
Position: Plant Technician Commercial Boilers (High Temperature Hot Water) Location: Burghfield Role: Permanent Morson Talent is excited to present a fantastic opportunity for a Plant Operator to join a company that has received significant investment and operates on an impressive 225-acre site. Our client specialises in research and production activities for the Ministry of Defence, contributing to national defence and security efforts. As a Plant Technician, your primary responsibility will be to provide essential maintenance and support for all High-Temperature Hot Water (HTHW) operations. Role Responsibilities: • Monitor HTHW plant and associated equipment, conducting safety equipment tests • Capable of safely shutting down and securing any malfunctioning equipment that poses a safety risk, and promptly notifying relevant engineers for maintenance • Support the HTHW supervisor with planned, reactive, or project tasks while ensuring compliance with site procedures and safety protocols • Monitor, maintain, investigate, and address issues related to the site Building Management System (BMS) • Conduct regular plant checks, report any defects, and ensure cleanliness, tidiness, and safety in all HTHW plant rooms • Identify and report defects to the HTHW supervisor promptly • Provide efficient responses to customer inquiries and helpdesk requests • Ensure compliance with regulations and escalate any safety or security concerns to the appropriate authorities • Offer innovative solutions and suggestions to enhance processes, building infrastructure, plant, and systems • Cultivate collaborative relationships with end-users Skills and Qualifications: • Technical expertise, qualifications, or apprenticeship in High-Temperature Hot Water (HTHW) operations is essential • BOAS 9.2 certification • Familiarity with BG02 guidance on safe operation of hot water boilers • Knowledge of INDG436 guidelines for the safe management of industrial steam and hot water boilers • Understanding of PSSR regulations 2000 L122 ACOP • Proficiency in BMS systems • Experience with key operational procedures such as time sheets, planned maintenance systems, quality assurance, and health & safety protocols • Proven ability to effectively resolve customer issues within specific contracts • Smart and well-presented appearance • All candidates must undergo DV Clearance If you meet the requirements listed above and are eager to contribute to a vital role within a dynamic and forward-thinking organization, we encourage you to apply for this exciting opportunity. Please submit your application with a detailed CV showcasing your relevant experience and qualifications. We look forward to welcoming a talented and dedicated Plant Technician to our team. Morson Talent is an equal opportunities employer. JBRP1_UKTJ
Role: Electrical and Instrumentation Supervisor Location: Maidstone£Competitive + Company Bonus & Benefits inc free Healthcare, On-site gym, subsidised lunch, EAP schemes, financial assistance, etcHours: 8:00 am until 4:30 pm Our client, a leading international manufacturer, is currently recruiting for an experienced Electrical and Instrumentation Supervisor to join their growing team on a permanent contract. As the Electrical and Instrumentation Supervisor, you will have a key focus on front-line maintenance and will be required to help coordinate the engineering departments' daily and weekly prioritization, scheduling, and preparations of workload. This requires a strong focus on reliability and preventative maintenance to ensure problems are resolved the first time. The post holder will be responsible for all day-to-day electrical, instrumentation, and some control systems maintenance activities associated with the paper machine, Stock Prep plant, the winder, and its transport system.Duties include:- To take or initiate any corrective action necessary to ensure continuity of production. - Working closely with the Production Superintendents, Shift Production Managers, and E&I and Mechanical colleagues as the E&I engineering lead contact for day-to-day and immediate machine problems. - Taking evaluation of morning production meeting problems to the engineering team so that they plan and coordinate the resolution. - All equipment contained within the PM9 machine house except for those under a specialist service contract, although there may be times when they will need support, direction, or some involvement from the Engineering team.- Take responsibility for the Electrical & Instrumentation area of the engineering workshops, including the test room, PAT testing, workbenches, and the general condition of the working area in line with 5S principles. - Use SAP MM for BOM and spare part information. What we are looking for:- A Competent Electrical Engineer with a degree in Electrical Engineering or similar, orworking towards an Electrical Degree or equivalent.- Previous experience in an E & I Technician position.- NEBOSH safety certificateAt KHR we take care to ensure that you are represented as well as possible so it is worth checking your CV for layout, spelling and grammar as well as making sure it is up to date before you submit. If you feel you need to highlight particular qualifications, skills or relevant experience with regards to a specific role then please add a cover letter or a preface page. This does not need to be formatted in the same manner. In addition, if your CV is heavy with graphics etc, please could you also submit a "clean" copy in Word. Thank you.KH Recruitment Ltd is acting as an Employment Agency in relation to this vacancy. KHR - Recruitment Specialists is a trading name of KH Recruitment Ltd Keep in touch with us online for job alerts, industry updates and market
Apr 23, 2024
Full time
Role: Electrical and Instrumentation Supervisor Location: Maidstone£Competitive + Company Bonus & Benefits inc free Healthcare, On-site gym, subsidised lunch, EAP schemes, financial assistance, etcHours: 8:00 am until 4:30 pm Our client, a leading international manufacturer, is currently recruiting for an experienced Electrical and Instrumentation Supervisor to join their growing team on a permanent contract. As the Electrical and Instrumentation Supervisor, you will have a key focus on front-line maintenance and will be required to help coordinate the engineering departments' daily and weekly prioritization, scheduling, and preparations of workload. This requires a strong focus on reliability and preventative maintenance to ensure problems are resolved the first time. The post holder will be responsible for all day-to-day electrical, instrumentation, and some control systems maintenance activities associated with the paper machine, Stock Prep plant, the winder, and its transport system.Duties include:- To take or initiate any corrective action necessary to ensure continuity of production. - Working closely with the Production Superintendents, Shift Production Managers, and E&I and Mechanical colleagues as the E&I engineering lead contact for day-to-day and immediate machine problems. - Taking evaluation of morning production meeting problems to the engineering team so that they plan and coordinate the resolution. - All equipment contained within the PM9 machine house except for those under a specialist service contract, although there may be times when they will need support, direction, or some involvement from the Engineering team.- Take responsibility for the Electrical & Instrumentation area of the engineering workshops, including the test room, PAT testing, workbenches, and the general condition of the working area in line with 5S principles. - Use SAP MM for BOM and spare part information. What we are looking for:- A Competent Electrical Engineer with a degree in Electrical Engineering or similar, orworking towards an Electrical Degree or equivalent.- Previous experience in an E & I Technician position.- NEBOSH safety certificateAt KHR we take care to ensure that you are represented as well as possible so it is worth checking your CV for layout, spelling and grammar as well as making sure it is up to date before you submit. If you feel you need to highlight particular qualifications, skills or relevant experience with regards to a specific role then please add a cover letter or a preface page. This does not need to be formatted in the same manner. In addition, if your CV is heavy with graphics etc, please could you also submit a "clean" copy in Word. Thank you.KH Recruitment Ltd is acting as an Employment Agency in relation to this vacancy. KHR - Recruitment Specialists is a trading name of KH Recruitment Ltd Keep in touch with us online for job alerts, industry updates and market
Mechanical Technician - up to £28 per hour Inside IR35 - 12 Months (extensions highly likely) Herefordshire - standard 37 hours - Fully Onsite Working (Free Parking).Apprenticeship and NVQ needed* One stage F2F interview with skills test - Sector: Aerospace and Defence Are you a skilled production professional seeking a challenging opportunity with a leading company in the manufacturing sector? We are currently looking for dedicated individuals to join the Operations team of Our client who is a renowned Aerospace company at the forefront of space exploration and travel. Daily tasks will include assembly and final assembly processes of aluminium composite panel manufacture. Responsibilities: * Able to insert panels with the correct type of mechanical fasteners. * Potting of inserts * Bonding of various brackets and equipment * Bonding of inserts, using various adhesives * Bonding components and sub-assemblies using adhesives to drawing specifications * Produce work to drawing specification * Ability to read and understand Detailed engineering drawings and procedures. * Awareness and adherence to all the company Health & Safety procedures * High tolerance requirements (typically better than 0.05mm in various areas). Essential: Previous experience in a Manual Handling Role Previous experience within a production/manufacturing environment with regular use of hand tools Ability to follow procedures and work instructions/manuals. Relevant experience in carbon fibre A relevant Apprenticeship or NVQ Desirable: Clean room environment experience Previous experience of laminating Aluminium Ability to read and interpret engineering drawings preferred
Apr 23, 2024
Contractor
Mechanical Technician - up to £28 per hour Inside IR35 - 12 Months (extensions highly likely) Herefordshire - standard 37 hours - Fully Onsite Working (Free Parking).Apprenticeship and NVQ needed* One stage F2F interview with skills test - Sector: Aerospace and Defence Are you a skilled production professional seeking a challenging opportunity with a leading company in the manufacturing sector? We are currently looking for dedicated individuals to join the Operations team of Our client who is a renowned Aerospace company at the forefront of space exploration and travel. Daily tasks will include assembly and final assembly processes of aluminium composite panel manufacture. Responsibilities: * Able to insert panels with the correct type of mechanical fasteners. * Potting of inserts * Bonding of various brackets and equipment * Bonding of inserts, using various adhesives * Bonding components and sub-assemblies using adhesives to drawing specifications * Produce work to drawing specification * Ability to read and understand Detailed engineering drawings and procedures. * Awareness and adherence to all the company Health & Safety procedures * High tolerance requirements (typically better than 0.05mm in various areas). Essential: Previous experience in a Manual Handling Role Previous experience within a production/manufacturing environment with regular use of hand tools Ability to follow procedures and work instructions/manuals. Relevant experience in carbon fibre A relevant Apprenticeship or NVQ Desirable: Clean room environment experience Previous experience of laminating Aluminium Ability to read and interpret engineering drawings preferred
Position: Mechanical Technician Pay rate: £23.82 p/h inside IR35. location: Stevenage, UK Role Type: 12 Month contract with extension Position: Onsite IO Associates seeks a Panels Surface Treatments Technician for the Stevenage site . Join a global aerospace leader specializing in commercial and military aircraft, helicopters, defense, and space sectors. This role offers a chance to contribute to innovative projects within a dynamic team shaping the future of aviation and space systems. Responsibilities Collaborating within an AIT Operations team to consistently meet quality standards and adhere to production plans. Following LDS guidelines for methods and procedures, while ensuring compliance with standard processes, area requirements, and safety protocols. Upholding Cleanroom Regulations, local safety guidelines, and the 5S policy within the work area. Providing progress updates to Lead Technicians or Team Leads as needed, participating in shop floor meetings, supporting trainees, and contributing to continuous improvement efforts. Skills required Proficient in interpreting detailed drawings and electronic work instructions within prescribed procedures. Skilled in following procedures with defined checkpoints and quality gates. Experienced in various industries such as Space, Aerospace, Automotive, Motorsport, etc. Capable of working at elevated heights. Competent in preparing paint compounds according to manufacturer specifications. This is an excellent opportunity to work for an international company that encourages and facilitates personal growth. Please apply or get in touch with Munish or Email
Apr 22, 2024
Contractor
Position: Mechanical Technician Pay rate: £23.82 p/h inside IR35. location: Stevenage, UK Role Type: 12 Month contract with extension Position: Onsite IO Associates seeks a Panels Surface Treatments Technician for the Stevenage site . Join a global aerospace leader specializing in commercial and military aircraft, helicopters, defense, and space sectors. This role offers a chance to contribute to innovative projects within a dynamic team shaping the future of aviation and space systems. Responsibilities Collaborating within an AIT Operations team to consistently meet quality standards and adhere to production plans. Following LDS guidelines for methods and procedures, while ensuring compliance with standard processes, area requirements, and safety protocols. Upholding Cleanroom Regulations, local safety guidelines, and the 5S policy within the work area. Providing progress updates to Lead Technicians or Team Leads as needed, participating in shop floor meetings, supporting trainees, and contributing to continuous improvement efforts. Skills required Proficient in interpreting detailed drawings and electronic work instructions within prescribed procedures. Skilled in following procedures with defined checkpoints and quality gates. Experienced in various industries such as Space, Aerospace, Automotive, Motorsport, etc. Capable of working at elevated heights. Competent in preparing paint compounds according to manufacturer specifications. This is an excellent opportunity to work for an international company that encourages and facilitates personal growth. Please apply or get in touch with Munish or Email
Join Maintenance at one of our six world class manufacturing sites in Haverhill, UK to play a crucial role in delivering our portfolio of active pharmaceutical ingredients. Working in Calibration and Metrology you will be responsible for instrument calibration needs across the site. Your Responsibilities You will: Work collaboratively across a 9 hectare site to deliver on calibration needs. You will communicate with a range of teams and your role may include working in clean rooms, labs, production, manufacturing, warehouse and with external contractors. Take accountability as part of the Metrology team to maintain & calibrate operational process equipment and complete documentation in line with GMP, safety, quality and validation protocols to achieve site compliance. Regularly review performance of equiptment to minimize equipment downtime and troubleshoot equipment failures and effect repairs. Our Company EUROAPI is a new player in Active Pharmaceutical Ingredients (API), carve out from Sanofi with the purpose of becoming a worldwide champion in API commercial and Contract Development and Manufacturing Organization (CDMO) activities. Taking action for health by enabling access to essential therapies inspires our 3,350 people every day. Headquartered in Paris, Euroapi include 6 European API production sites located in Brindisi (Italy), Frankfurt (Germany), Haverhill (UK), St Aubin les Elbeuf (France), Budapest (Hungary) and Vertolaye (France). The EUROAPI Haverhill (UK) site has been established for 40 years and is located 15 miles east of Cambridge and 60 miles north of London, within the golden triangle. It employs over 250 people and has built a strong reputation in Active Pharmaceutical Ingredient (API) Spray Drying and Contract Development and Manufacturing Organisation (CDMO). Haverhill is proud to house the world's largest, continuous production, pharmaceutical spray dryer and performs secondary packaging and release activities for oncology and rare disease medicines supporting global markets. The site is also developing a contract testing and release facility within its laboratories. Our Requirements Proven experience in a maintenance role - reactive and preventative with hands on experience in carrying out scheduled calibration routines i.e. temp, pressure and flow. Instrumentation background - qualified by apprenticeship with a BTEC/HND or similar in instrumentation or electronic engineering. Forward thinking safety mindset with experience in maintaining documentation according to regulatory and compliance standards. Experience in the pharmaceutical (GxP), chemicals or energy sectors would highly be beneficial. Your Benefits 36 hours per week Monday to Friday, 8am start with an earlier finish on Friday. Attractive, competitive salary. Annual bonus. Overtime eligibility. Company paid medical, life assurance and dental insurance. Market leading reward boost scheme. A fantastic wellbeing team that run a range of initiatives on and off site. 14 weeks of paid parental leave at 100% of salary for any employee. 5 weeks annual leave with the opportunity to buy/sell 5 days per year. Support for development through training & courses relevant to your role. Culture & Values at Euroapi We bring our culture to life in the way we work every day. Our culture enables career development and talent management, we recognise that how we do things is as important as what we do, and our values set out how we achieve our goals and help us "do it right". Our values & behaviours are based on the following pillars: We empower our people for greater positive impact. We create value by putting our clients at the centre of everything we do. We are accountable for what we do, always acting with the company's interest in mind. We value and respect all our stakeholders. Culture & Values at EUROAPI We bring our culture to life in the way we work every day. Our culture enables career development and talent management, we recognise that how we do things is as important as what we do, and our values set out how we achieve our goals and help us "do it right". Diversity & Inclusion EUROAPI is committed to nurturing a culture of diversity and inclusion that contributes to improving innovation, performance, and engagement. We value transparency, mutual respect, and equal treatment of people. For this reason, we are firm in protecting our employees against any forms of discrimination. We are Disability Confiden t - Committed which means we make reasonable adjustments to our process and offer interviews to disabled people who meet the minimum criteria for our vacancies. If you would like any assistance or require the application to be completed in a different format, please call or contact our Haverhill site reception. Environment, Social and Governance We strongly believe that the success of our company lies in its capacity to adapt to tomorrow's challenges. Our responsibility as a company is to provide sustainability and resilience to the pharmaceutical value chain.
Feb 01, 2024
Full time
Join Maintenance at one of our six world class manufacturing sites in Haverhill, UK to play a crucial role in delivering our portfolio of active pharmaceutical ingredients. Working in Calibration and Metrology you will be responsible for instrument calibration needs across the site. Your Responsibilities You will: Work collaboratively across a 9 hectare site to deliver on calibration needs. You will communicate with a range of teams and your role may include working in clean rooms, labs, production, manufacturing, warehouse and with external contractors. Take accountability as part of the Metrology team to maintain & calibrate operational process equipment and complete documentation in line with GMP, safety, quality and validation protocols to achieve site compliance. Regularly review performance of equiptment to minimize equipment downtime and troubleshoot equipment failures and effect repairs. Our Company EUROAPI is a new player in Active Pharmaceutical Ingredients (API), carve out from Sanofi with the purpose of becoming a worldwide champion in API commercial and Contract Development and Manufacturing Organization (CDMO) activities. Taking action for health by enabling access to essential therapies inspires our 3,350 people every day. Headquartered in Paris, Euroapi include 6 European API production sites located in Brindisi (Italy), Frankfurt (Germany), Haverhill (UK), St Aubin les Elbeuf (France), Budapest (Hungary) and Vertolaye (France). The EUROAPI Haverhill (UK) site has been established for 40 years and is located 15 miles east of Cambridge and 60 miles north of London, within the golden triangle. It employs over 250 people and has built a strong reputation in Active Pharmaceutical Ingredient (API) Spray Drying and Contract Development and Manufacturing Organisation (CDMO). Haverhill is proud to house the world's largest, continuous production, pharmaceutical spray dryer and performs secondary packaging and release activities for oncology and rare disease medicines supporting global markets. The site is also developing a contract testing and release facility within its laboratories. Our Requirements Proven experience in a maintenance role - reactive and preventative with hands on experience in carrying out scheduled calibration routines i.e. temp, pressure and flow. Instrumentation background - qualified by apprenticeship with a BTEC/HND or similar in instrumentation or electronic engineering. Forward thinking safety mindset with experience in maintaining documentation according to regulatory and compliance standards. Experience in the pharmaceutical (GxP), chemicals or energy sectors would highly be beneficial. Your Benefits 36 hours per week Monday to Friday, 8am start with an earlier finish on Friday. Attractive, competitive salary. Annual bonus. Overtime eligibility. Company paid medical, life assurance and dental insurance. Market leading reward boost scheme. A fantastic wellbeing team that run a range of initiatives on and off site. 14 weeks of paid parental leave at 100% of salary for any employee. 5 weeks annual leave with the opportunity to buy/sell 5 days per year. Support for development through training & courses relevant to your role. Culture & Values at Euroapi We bring our culture to life in the way we work every day. Our culture enables career development and talent management, we recognise that how we do things is as important as what we do, and our values set out how we achieve our goals and help us "do it right". Our values & behaviours are based on the following pillars: We empower our people for greater positive impact. We create value by putting our clients at the centre of everything we do. We are accountable for what we do, always acting with the company's interest in mind. We value and respect all our stakeholders. Culture & Values at EUROAPI We bring our culture to life in the way we work every day. Our culture enables career development and talent management, we recognise that how we do things is as important as what we do, and our values set out how we achieve our goals and help us "do it right". Diversity & Inclusion EUROAPI is committed to nurturing a culture of diversity and inclusion that contributes to improving innovation, performance, and engagement. We value transparency, mutual respect, and equal treatment of people. For this reason, we are firm in protecting our employees against any forms of discrimination. We are Disability Confiden t - Committed which means we make reasonable adjustments to our process and offer interviews to disabled people who meet the minimum criteria for our vacancies. If you would like any assistance or require the application to be completed in a different format, please call or contact our Haverhill site reception. Environment, Social and Governance We strongly believe that the success of our company lies in its capacity to adapt to tomorrow's challenges. Our responsibility as a company is to provide sustainability and resilience to the pharmaceutical value chain.
Production Technician We are looking to recruit a Production Technician with experience in high precision equipment manufacturing to join an exciting and rapidly growing technology development company based in Hertfordshire. As the Production Technician, you will use your extensive expertise in precision assembly and manufacturing in a lab environment to support production and development activities. Production Technician's Responsibilities: Assembling ultra-precision components and subassemblies to high tolerances while following standard operating procedures. Using a range of automated processing equipment and measuring machines to check components against specification to achieve precision alignment of assemblies to micron level tolerances. Working in a close collaboration with the team supporting the smooth and safe running of the production process and facilities. Requirements: Experience working in precision assembly and manufacturing, in a high technology engineering environment, such as scientific instruments, microfluidic device fabrication or semiconductor processing Hands-on experience in at least two of the following areas: Cleanroom processing and fabrication, use of microscopes and other measuring equipment, precision mechanical assembly, Micromachining, Micron-scale moulding and replication. Being skilled in precision manual procedures and handling delicate components, ability to accurately follow standard operating procedures. Experience working as part of a team, recording and communicating observations and measurements
Dec 15, 2022
Full time
Production Technician We are looking to recruit a Production Technician with experience in high precision equipment manufacturing to join an exciting and rapidly growing technology development company based in Hertfordshire. As the Production Technician, you will use your extensive expertise in precision assembly and manufacturing in a lab environment to support production and development activities. Production Technician's Responsibilities: Assembling ultra-precision components and subassemblies to high tolerances while following standard operating procedures. Using a range of automated processing equipment and measuring machines to check components against specification to achieve precision alignment of assemblies to micron level tolerances. Working in a close collaboration with the team supporting the smooth and safe running of the production process and facilities. Requirements: Experience working in precision assembly and manufacturing, in a high technology engineering environment, such as scientific instruments, microfluidic device fabrication or semiconductor processing Hands-on experience in at least two of the following areas: Cleanroom processing and fabrication, use of microscopes and other measuring equipment, precision mechanical assembly, Micromachining, Micron-scale moulding and replication. Being skilled in precision manual procedures and handling delicate components, ability to accurately follow standard operating procedures. Experience working as part of a team, recording and communicating observations and measurements
The role is a Permanent Fabric Technician role with a lot of room for Progression. Client Details The client's mission is to make world class theatre that's entertaining, challenging and inspiring - and to make it for everyone. It aims to reach the widest possible audience and to be as inclusive, diverse and national as possible with a broad range of productions that play in London, on tour around the UK, on Broadway and across the globe. Description 1. To work with the Facilities team on all installation, maintenance, modifications of all building structures and fittings at the client's site and its other sites.2. You may be required to work with other NT Technical Departments at the request of the relevant Managers and assist with the Facilities M&E department.3. To carry out routine Lamping, cleaning, maintenance and replacement of plant and other consumable items and assist Engineers where required. To provide assistance to all Trades/Crafts/ Apprentices as directed by your Supervisor.4. To carry out weekly flushing and temperature tests following the latest L8 Legionella Testing and Compliance Guidance, ensuring Management Log is kept up to date (Training will be given).5. To assist with the building familiarisation for new members of staff.6. Liaise with National Theatre personnel, contractors and visitors to assist in the smooth running of events. Profile The ability to work as part of a team and on your own initiative, without supervision The ability to remain calm under pressure, in stressful situations, and in an emergency The ability to communicate effectively with staff, and members of the public, in a courteous and diplomatic manner. Ability to demonstrate high levels of adaptability; quick to take on board new ideas, logical in addressing technical or customer related issues and a flexible approach when doing tasks Punctual with strong time management skills and working to tight deadlines A strong focus and experience of delivering excellent customer service. Job Offer On offer for The Candidate is: Competitive Salary Great Progression
Dec 08, 2022
Full time
The role is a Permanent Fabric Technician role with a lot of room for Progression. Client Details The client's mission is to make world class theatre that's entertaining, challenging and inspiring - and to make it for everyone. It aims to reach the widest possible audience and to be as inclusive, diverse and national as possible with a broad range of productions that play in London, on tour around the UK, on Broadway and across the globe. Description 1. To work with the Facilities team on all installation, maintenance, modifications of all building structures and fittings at the client's site and its other sites.2. You may be required to work with other NT Technical Departments at the request of the relevant Managers and assist with the Facilities M&E department.3. To carry out routine Lamping, cleaning, maintenance and replacement of plant and other consumable items and assist Engineers where required. To provide assistance to all Trades/Crafts/ Apprentices as directed by your Supervisor.4. To carry out weekly flushing and temperature tests following the latest L8 Legionella Testing and Compliance Guidance, ensuring Management Log is kept up to date (Training will be given).5. To assist with the building familiarisation for new members of staff.6. Liaise with National Theatre personnel, contractors and visitors to assist in the smooth running of events. Profile The ability to work as part of a team and on your own initiative, without supervision The ability to remain calm under pressure, in stressful situations, and in an emergency The ability to communicate effectively with staff, and members of the public, in a courteous and diplomatic manner. Ability to demonstrate high levels of adaptability; quick to take on board new ideas, logical in addressing technical or customer related issues and a flexible approach when doing tasks Punctual with strong time management skills and working to tight deadlines A strong focus and experience of delivering excellent customer service. Job Offer On offer for The Candidate is: Competitive Salary Great Progression
About This Role We have a new opportunity for a Quality Control Radiochemist to join our Radiopharmacy site in Sutton. This is a full time position working 40 hours a week with a salary of between £31,000 - £40,000 (dependant on experience). Ideally you should be a scientific graduate with an Analytical Chemistry background, ideally with experience of (radio) pharmaceutical QC in a GMP environment. Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date. Radiochemist (Quality Control) Main Role Undertake the quality control operations to be carried out in respect of each batch of PET radiopharmaceuticals prior to release for patient use. Duties & Responsibilities QC routines Operate and maintain routine protocols for the Erigal chemistry laboratory including the production of standard 18FDG synthesis and other PET tracers in strict adherence to GMP and relevant EU pharmacopoeia standards. Manage raw material sampling, testing and release system. Maintenance Ensure efficient performance of, and undertake first-line maintenance of, Quality Control equipment including HPLC (radiochemical and chemical purity of 18F FDG), Gas Chromatography, pH measurement, Osmolality and LAL. Faults Maintain records of faults on any dysfunction - operational or equipment. Quality Systems In association with the QP to develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for standard PET tracers. Timetable Undertake function no.1 above in accordance with a pre-determined daily timetable. Materials Ordering of chemicals, glassware, cleaning and other consumables for routine QC analysis. Formulation of reagents for radiochemistry, mixing of solvents for HPLC and other analyses, cleaning of glassware and disposal of waste chemicals and materials. Standard Operating Procedures Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the QP and adoption by the unit. Training Others Provide training and support for others selected as rota / backup in undertaking routine QC operations. R & D Search out, promote and manage R& D initiatives that both enhance the reputation of Erigal and their professional staffs as is consistent within approved budgets and grants. Skills in Radiochemistry Develop necessary skills to advise and support radiochemical laboratory technician/s with specific reference to the functions of Synthesis and Dispensing of radiotracers. Maintain understanding of best practice and changes in requirements for QC analytical testing. Safety and Control Assume responsibility for the safe and efficient handling of all radioactive sample substances (solid, gas, liquid) received from the Hot Cells room for QC tests including their movement, storage, containerisation and decay control. In accordance with local rules for emergency or serious incident procedure record such events in accordance with SOPs. Responsible for following agreed safety procedures to ensure safety of yourself and others. Regulatory Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules developed by Erigal in conformity to such licensing requirement. Alliance Medical Values Alliance Medical Values: Leaders, managers, and supervisors have a particular responsibility to be role models in terms of how they demonstrate these values themselves and how they engage their teams to work in this way. Collaboration: We work together and in partnership for all our patients. We respect expertise and combine it to achieve more. Excellence: We never compromise. We strive to deliver the very best in everything we do to ensure the highest quality of care. We treat our patients and each other with compassion, dignity and respect. Learning: Knowledge and understanding comes from learning. At Alliance Medical we are committed to ensuring that each and every one of us keeps on learning and that we continuously look for improved ways of working. Efficiency: Efficiency in healthcare means more patients get better care. We constantly seek new ways to use the scarce resource of healthcare more intelligently so that more people can live longer, fuller lives. Openness: We act with transparency and honesty in everything we do, where staff are encouraged to speak up to ensure a safe and secure environment for our patients.
Sep 23, 2022
Full time
About This Role We have a new opportunity for a Quality Control Radiochemist to join our Radiopharmacy site in Sutton. This is a full time position working 40 hours a week with a salary of between £31,000 - £40,000 (dependant on experience). Ideally you should be a scientific graduate with an Analytical Chemistry background, ideally with experience of (radio) pharmaceutical QC in a GMP environment. Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date. Radiochemist (Quality Control) Main Role Undertake the quality control operations to be carried out in respect of each batch of PET radiopharmaceuticals prior to release for patient use. Duties & Responsibilities QC routines Operate and maintain routine protocols for the Erigal chemistry laboratory including the production of standard 18FDG synthesis and other PET tracers in strict adherence to GMP and relevant EU pharmacopoeia standards. Manage raw material sampling, testing and release system. Maintenance Ensure efficient performance of, and undertake first-line maintenance of, Quality Control equipment including HPLC (radiochemical and chemical purity of 18F FDG), Gas Chromatography, pH measurement, Osmolality and LAL. Faults Maintain records of faults on any dysfunction - operational or equipment. Quality Systems In association with the QP to develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for standard PET tracers. Timetable Undertake function no.1 above in accordance with a pre-determined daily timetable. Materials Ordering of chemicals, glassware, cleaning and other consumables for routine QC analysis. Formulation of reagents for radiochemistry, mixing of solvents for HPLC and other analyses, cleaning of glassware and disposal of waste chemicals and materials. Standard Operating Procedures Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the QP and adoption by the unit. Training Others Provide training and support for others selected as rota / backup in undertaking routine QC operations. R & D Search out, promote and manage R& D initiatives that both enhance the reputation of Erigal and their professional staffs as is consistent within approved budgets and grants. Skills in Radiochemistry Develop necessary skills to advise and support radiochemical laboratory technician/s with specific reference to the functions of Synthesis and Dispensing of radiotracers. Maintain understanding of best practice and changes in requirements for QC analytical testing. Safety and Control Assume responsibility for the safe and efficient handling of all radioactive sample substances (solid, gas, liquid) received from the Hot Cells room for QC tests including their movement, storage, containerisation and decay control. In accordance with local rules for emergency or serious incident procedure record such events in accordance with SOPs. Responsible for following agreed safety procedures to ensure safety of yourself and others. Regulatory Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules developed by Erigal in conformity to such licensing requirement. Alliance Medical Values Alliance Medical Values: Leaders, managers, and supervisors have a particular responsibility to be role models in terms of how they demonstrate these values themselves and how they engage their teams to work in this way. Collaboration: We work together and in partnership for all our patients. We respect expertise and combine it to achieve more. Excellence: We never compromise. We strive to deliver the very best in everything we do to ensure the highest quality of care. We treat our patients and each other with compassion, dignity and respect. Learning: Knowledge and understanding comes from learning. At Alliance Medical we are committed to ensuring that each and every one of us keeps on learning and that we continuously look for improved ways of working. Efficiency: Efficiency in healthcare means more patients get better care. We constantly seek new ways to use the scarce resource of healthcare more intelligently so that more people can live longer, fuller lives. Openness: We act with transparency and honesty in everything we do, where staff are encouraged to speak up to ensure a safe and secure environment for our patients.
About This Role We have an exciting opportunity for a Production Radiochemist to join us on a 12 month Fixed Term Contract at our Guildford Radiopharmacy. We also have a second vacancy for a Production Radiochemist on a permanent contract. Please state in your application if you are interested in the Fixed Term or Permanent position. These are full time positions working 40 hours a week (Monday-Sunday) with a salary circa £31,000. Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date. Radiochemist (Production) Main Role Undertake production of Fluorine-18 (18F) and radio-synthesis of 18F radiopharmaceuticals for PET imaging. Duties & Responsibilities Production Operate and maintain protocols for the manufacture of 18F and for the Alliance Medical Radiopharmacy chemistry laboratory including the production synthesis of standard 18FDG, 18Ethylcholine (18FEC), and other PET tracers in strict adherence to GMP and relevant EU pharmacopoeia standards. Operate routine protocols for customer orders and distribution of 18FDG and other PET tracers to sites. Maintenance Arrange first-line scheduled and emergency maintenance for the cyclotron and associated plant, in collaboration with GE engineers. Participate in GE training courses and maintain links with the GE Medical Systems, Sweden and other 'PETtrace' centres. Ensure efficient performance of, and undertake first-line maintenance of, the FDG & FEC Synthesisers, Dispensing Equipment, Hot Cells, including dose calibration, monitoring and sterility checks within the context of strict application of environmental and 'clean room' protocols. Faults Maintain records of faults on any dysfunction - operational, equipment or environment integrity. Interpret and rectify operational faults where possible and indicate where the GE engineer or contractor should be called. Quality Systems Develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for all aspects of cyclotron operations, and radiopharmaceutical production of standard PET tracers Principal Operator/Timetable On a rota basis, act as either cyclotron principal operator or as principal laboratory technician for radio-synthesis of PET tracers in accordance with a pre-determined daily timetable. Targetary Maintain routine protocols for production of standard 18F and other PET targetary in accordance with GMP guidelines. Maintenance and Engineering Services Support appropriate Maintenance/Engineering arrangements to ensure reliable delivery of critical services including air handling, chilled water, gases, electric power and security. Chemical Preparation Ordering of stock, preparation of chemicals required for routine radiochemistry production including formulation of reagents, etc and the safe disposal of waste chemicals and materials. Standard Operating Procedures Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the QP and adoption by the unit. Training Others Provide training and support for others selected as rota/backup in cyclotron operation and production of Radiopharmaceuticals. R & D Search out, promote and manage R&D initiatives that both enhance the reputation of Alliance Medical Radiopharmacy and their professional staffs as is consistent within approved budgets and grants. Skills in Radiochemistry Develop necessary skills to provide relief and rota support to radiochemical laboratory technician/s with specific reference to the functions of: Operation of cyclotron. Production of Radioisotopes Safety and Control Assume responsibility for the safe and efficient handling of all radioactive substances (solid, gas, liquid) received from the Centre's cyclotron including their synthesis, transmission, dispensing, storage, containerisation, packing, despatch, transport, decay control, and release. In accordance with local rules for emergency or serious incident procedure record such events in accordance with SOPs. Responsible for following agreed safety procedures to ensure safety of yourself and others. Regulatory Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules developed by Alliance Medical Radiopharmacy in conformity to such licensing requirement. Alliance Medical Values Alliance Medical Values: Leaders, managers, and supervisors have a particular responsibility to be role models in terms of how they demonstrate these values themselves and how they engage their teams to work in this way. Collaboration: We work together and in partnership for all our patients. We respect expertise and combine it to achieve more. Excellence: We never compromise. We strive to deliver the very best in everything we do to ensure the highest quality of care. We treat our patients and each other with compassion, dignity and respect. Learning: Knowledge and understanding comes from learning. At Alliance Medical we are committed to ensuring that each and every one of us keeps on learning and that we continuously look for improved ways of working. Efficiency: Efficiency in healthcare means more patients get better care. We constantly seek new ways to use the scarce resource of healthcare more intelligently so that more people can live longer, fuller lives. Openness: We act with transparency and honesty in everything we do, where staff are encouraged to speak up to ensure a safe and secure environment for our patients. Additional note This Job Description is not inflexible, but is an outline and account of the main duties of the position. Any changes will be discussed with the job holder in advance. The Job Description will be reviewed periodically to take into account changes and/or developments in service requirements.
Sep 23, 2022
Full time
About This Role We have an exciting opportunity for a Production Radiochemist to join us on a 12 month Fixed Term Contract at our Guildford Radiopharmacy. We also have a second vacancy for a Production Radiochemist on a permanent contract. Please state in your application if you are interested in the Fixed Term or Permanent position. These are full time positions working 40 hours a week (Monday-Sunday) with a salary circa £31,000. Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date. Radiochemist (Production) Main Role Undertake production of Fluorine-18 (18F) and radio-synthesis of 18F radiopharmaceuticals for PET imaging. Duties & Responsibilities Production Operate and maintain protocols for the manufacture of 18F and for the Alliance Medical Radiopharmacy chemistry laboratory including the production synthesis of standard 18FDG, 18Ethylcholine (18FEC), and other PET tracers in strict adherence to GMP and relevant EU pharmacopoeia standards. Operate routine protocols for customer orders and distribution of 18FDG and other PET tracers to sites. Maintenance Arrange first-line scheduled and emergency maintenance for the cyclotron and associated plant, in collaboration with GE engineers. Participate in GE training courses and maintain links with the GE Medical Systems, Sweden and other 'PETtrace' centres. Ensure efficient performance of, and undertake first-line maintenance of, the FDG & FEC Synthesisers, Dispensing Equipment, Hot Cells, including dose calibration, monitoring and sterility checks within the context of strict application of environmental and 'clean room' protocols. Faults Maintain records of faults on any dysfunction - operational, equipment or environment integrity. Interpret and rectify operational faults where possible and indicate where the GE engineer or contractor should be called. Quality Systems Develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for all aspects of cyclotron operations, and radiopharmaceutical production of standard PET tracers Principal Operator/Timetable On a rota basis, act as either cyclotron principal operator or as principal laboratory technician for radio-synthesis of PET tracers in accordance with a pre-determined daily timetable. Targetary Maintain routine protocols for production of standard 18F and other PET targetary in accordance with GMP guidelines. Maintenance and Engineering Services Support appropriate Maintenance/Engineering arrangements to ensure reliable delivery of critical services including air handling, chilled water, gases, electric power and security. Chemical Preparation Ordering of stock, preparation of chemicals required for routine radiochemistry production including formulation of reagents, etc and the safe disposal of waste chemicals and materials. Standard Operating Procedures Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the QP and adoption by the unit. Training Others Provide training and support for others selected as rota/backup in cyclotron operation and production of Radiopharmaceuticals. R & D Search out, promote and manage R&D initiatives that both enhance the reputation of Alliance Medical Radiopharmacy and their professional staffs as is consistent within approved budgets and grants. Skills in Radiochemistry Develop necessary skills to provide relief and rota support to radiochemical laboratory technician/s with specific reference to the functions of: Operation of cyclotron. Production of Radioisotopes Safety and Control Assume responsibility for the safe and efficient handling of all radioactive substances (solid, gas, liquid) received from the Centre's cyclotron including their synthesis, transmission, dispensing, storage, containerisation, packing, despatch, transport, decay control, and release. In accordance with local rules for emergency or serious incident procedure record such events in accordance with SOPs. Responsible for following agreed safety procedures to ensure safety of yourself and others. Regulatory Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules developed by Alliance Medical Radiopharmacy in conformity to such licensing requirement. Alliance Medical Values Alliance Medical Values: Leaders, managers, and supervisors have a particular responsibility to be role models in terms of how they demonstrate these values themselves and how they engage their teams to work in this way. Collaboration: We work together and in partnership for all our patients. We respect expertise and combine it to achieve more. Excellence: We never compromise. We strive to deliver the very best in everything we do to ensure the highest quality of care. We treat our patients and each other with compassion, dignity and respect. Learning: Knowledge and understanding comes from learning. At Alliance Medical we are committed to ensuring that each and every one of us keeps on learning and that we continuously look for improved ways of working. Efficiency: Efficiency in healthcare means more patients get better care. We constantly seek new ways to use the scarce resource of healthcare more intelligently so that more people can live longer, fuller lives. Openness: We act with transparency and honesty in everything we do, where staff are encouraged to speak up to ensure a safe and secure environment for our patients. Additional note This Job Description is not inflexible, but is an outline and account of the main duties of the position. Any changes will be discussed with the job holder in advance. The Job Description will be reviewed periodically to take into account changes and/or developments in service requirements.
Mouldshop Technician 1 x continental Days and 1 x Nights Salary: Continental days £34000 - £37000, Nights £35000 - £41000 (plus private Medical) Do you want to work for a company where you can develop? What's in it for me? We offer a range of attractive staff benefits including accessible employee forums, comprehensive pension packages, flexible working arrangements, private medical healthcare for all employees and inclusive employment practices. This role will focus on: Working primarily within the clean rooms, where our mould machines are located, this role is responsible for tool changes and machine setting, and ensuring our moulding machines are running at their most efficient production rates to ensure maximum output. Additionally, this role will work closely with Supervisors and Operators to ensure correct and safe use of our machines. Carrying out mould tool changes as required- assisted by Tool Hangers Troubleshoot tooling/machinery defects to conclusion Drive the OEE system via SMED and ensure continuous improvement Drive the OEE system with cycle times, scrap reduction & downtime reduction Ensure first-off products meet the required standard before submitting for Quality Control Organise mould tool repairs, servicing and lot number updates Carry out maintenance activities in all production areas as required Facilitate plant servicing and repair by suppliers' engineers Support production requirements when necessary Provide training to production staff as required Provide continual support to Mouldshop Supervisors and Assembly Team Leaders To be successful in this role, youwill need: Technical experienceof injection moulding mould tool setting, ideally in a medical/ pharmaceuticalenvironment NVQ level 2 IMT qualification or equivalent experience Ability to effectively communicate to a wide range ofcolleagues Knowledge of manufacture to BS EN ISO 9001 and cGMP standards isdesirable Awareness of BS EN ISO 14644 clean room requirements isdesirable As a growing and ambitious organisation with a presence in over60 global locations and across multiple markets, we can offer you the workingenvironment and support needed to be successful. We are committed toachieving workforce diversity and creating an inclusive working environment. Wewelcome all applications irrespective of social and cultural background, age,gender, disability, sexual orientation or religious belief. About Watson Marlow Every day, we help companies across the globe to bemore efficient and sustainable. Watson-Marlow FluidTechnology Group (WMFTG) is the world leader in niche peristaltic pumps andassociated fluid path technologies. Comprising ten established brands, eachwith their area of expertise, but together offering our customers unrivalledsolutions for their pumping and fluid transfer applications. Together with our colleagues across Spirax- Sarco Engineeringplc, we are proud to be a FTSE 100 company.
Sep 06, 2022
Full time
Mouldshop Technician 1 x continental Days and 1 x Nights Salary: Continental days £34000 - £37000, Nights £35000 - £41000 (plus private Medical) Do you want to work for a company where you can develop? What's in it for me? We offer a range of attractive staff benefits including accessible employee forums, comprehensive pension packages, flexible working arrangements, private medical healthcare for all employees and inclusive employment practices. This role will focus on: Working primarily within the clean rooms, where our mould machines are located, this role is responsible for tool changes and machine setting, and ensuring our moulding machines are running at their most efficient production rates to ensure maximum output. Additionally, this role will work closely with Supervisors and Operators to ensure correct and safe use of our machines. Carrying out mould tool changes as required- assisted by Tool Hangers Troubleshoot tooling/machinery defects to conclusion Drive the OEE system via SMED and ensure continuous improvement Drive the OEE system with cycle times, scrap reduction & downtime reduction Ensure first-off products meet the required standard before submitting for Quality Control Organise mould tool repairs, servicing and lot number updates Carry out maintenance activities in all production areas as required Facilitate plant servicing and repair by suppliers' engineers Support production requirements when necessary Provide training to production staff as required Provide continual support to Mouldshop Supervisors and Assembly Team Leaders To be successful in this role, youwill need: Technical experienceof injection moulding mould tool setting, ideally in a medical/ pharmaceuticalenvironment NVQ level 2 IMT qualification or equivalent experience Ability to effectively communicate to a wide range ofcolleagues Knowledge of manufacture to BS EN ISO 9001 and cGMP standards isdesirable Awareness of BS EN ISO 14644 clean room requirements isdesirable As a growing and ambitious organisation with a presence in over60 global locations and across multiple markets, we can offer you the workingenvironment and support needed to be successful. We are committed toachieving workforce diversity and creating an inclusive working environment. Wewelcome all applications irrespective of social and cultural background, age,gender, disability, sexual orientation or religious belief. About Watson Marlow Every day, we help companies across the globe to bemore efficient and sustainable. Watson-Marlow FluidTechnology Group (WMFTG) is the world leader in niche peristaltic pumps andassociated fluid path technologies. Comprising ten established brands, eachwith their area of expertise, but together offering our customers unrivalledsolutions for their pumping and fluid transfer applications. Together with our colleagues across Spirax- Sarco Engineeringplc, we are proud to be a FTSE 100 company.
About This Role We have a new opportunity for a Production Radiochemist to join us at our Sutton Radiopharmacy Site. This is a full time position working 40 hours a week attracting a salary of £31,000. Ideally you are a scientific graduate with a scientific background, ideally with experience of (radio) pharmaceutical manufacture in a GMP environment. Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date. Radiochemist (Production) Main Role Undertake production of Fluorine-18 (18F) and radio-synthesis of 18F radiopharmaceuticals for PET imaging. Your place in our world Operations Manager Production Radiochemist Skills Required IT Skills Duties & Responsibilities Production Operate and maintain protocols for the manufacture of 18F and for the Alliance Medical Radiopharmacy chemistry laboratory including the production synthesis of standard 18FDG, 18Ethylcholine (18FEC), and other PET tracers in strict adherence to GMP and relevant EU pharmacopoeia standards. Operate routine protocols for customer orders and distribution of 18FDG and other PET tracers to sites. Maintenance Arrange first-line scheduled and emergency maintenance for the cyclotron and associated plant, in collaboration with GE engineers. Participate in GE training courses and maintain links with the GE Medical Systems, Sweden and other 'PETtrace' centres. Ensure efficient performance of, and undertake first-line maintenance of, the FDG & FEC Synthesisers, Dispensing Equipment, Hot Cells, including dose calibration, monitoring and sterility checks within the context of strict application of environmental and 'clean room' protocols. Faults Maintain records of faults on any dysfunction - operational, equipment or environment integrity. Interpret and rectify operational faults where possible and indicate where the GE engineer or contractor should be called. Quality Systems Develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for all aspects of cyclotron operations, and radiopharmaceutical production of standard PET tracers Principal Operator/Timetable On a rota basis, act as either cyclotron principal operator or as principal laboratory technician for radio-synthesis of PET tracers in accordance with a pre-determined daily timetable. Targetary Maintain routine protocols for production of standard 18F and other PET targetary in accordance with GMP guidelines. Maintenance and Engineering Services Support appropriate Maintenance/Engineering arrangements to ensure reliable delivery of critical services including air handling, chilled water, gases, electric power and security. Chemical Preparation Ordering of stock, preparation of chemicals required for routine radiochemistry production including formulation of reagents, etc and the safe disposal of waste chemicals and materials. Standard Operating Procedures Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the QP and adoption by the unit. Training Others Provide training and support for others selected as rota/backup in cyclotron operation and production of Radiopharmaceuticals. R & D Search out, promote and manage R&D initiatives that both enhance the reputation of Alliance Medical Radiopharmacy and their professional staffs as is consistent within approved budgets and grants. Skills in Radiochemistry Develop necessary skills to provide relief and rota support to radiochemical laboratory technician/s with specific reference to the functions of: Operation of cyclotron. Production of Radioisotopes Safety and Control Assume responsibility for the safe and efficient handling of all radioactive substances (solid, gas, liquid) received from the Centre's cyclotron including their synthesis, transmission, dispensing, storage, containerisation, packing, despatch, transport, decay control, and release. In accordance with local rules for emergency or serious incident procedure record such events in accordance with SOPs. Responsible for following agreed safety procedures to ensure safety of yourself and others. Regulatory Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules developed by Alliance Medical Radiopharmacy in conformity to such licensing requirement. Alliance Medical Values Alliance Medical Values: Leaders, managers, and supervisors have a particular responsibility to be role models in terms of how they demonstrate these values themselves and how they engage their teams to work in this way. Collaboration: We work together and in partnership for all our patients. We respect expertise and combine it to achieve more. Excellence: We never compromise. We strive to deliver the very best in everything we do to ensure the highest quality of care. We treat our patients and each other with compassion, dignity and respect. Learning: Knowledge and understanding comes from learning. At Alliance Medical we are committed to ensuring that each and every one of us keeps on learning and that we continuously look for improved ways of working. Efficiency: Efficiency in healthcare means more patients get better care. We constantly seek new ways to use the scarce resource of healthcare more intelligently so that more people can live longer, fuller lives. Openness: We act with transparency and honesty in everything we do, where staff are encouraged to speak up to ensure a safe and secure environment for our patients. Additional note This Job Description is not inflexible, but is an outline and account of the main duties of the position. Any changes will be discussed with the job holder in advance. The Job Description will be reviewed periodically to take into account changes and/or developments in service requirements.
Mar 30, 2022
Full time
About This Role We have a new opportunity for a Production Radiochemist to join us at our Sutton Radiopharmacy Site. This is a full time position working 40 hours a week attracting a salary of £31,000. Ideally you are a scientific graduate with a scientific background, ideally with experience of (radio) pharmaceutical manufacture in a GMP environment. Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date. Radiochemist (Production) Main Role Undertake production of Fluorine-18 (18F) and radio-synthesis of 18F radiopharmaceuticals for PET imaging. Your place in our world Operations Manager Production Radiochemist Skills Required IT Skills Duties & Responsibilities Production Operate and maintain protocols for the manufacture of 18F and for the Alliance Medical Radiopharmacy chemistry laboratory including the production synthesis of standard 18FDG, 18Ethylcholine (18FEC), and other PET tracers in strict adherence to GMP and relevant EU pharmacopoeia standards. Operate routine protocols for customer orders and distribution of 18FDG and other PET tracers to sites. Maintenance Arrange first-line scheduled and emergency maintenance for the cyclotron and associated plant, in collaboration with GE engineers. Participate in GE training courses and maintain links with the GE Medical Systems, Sweden and other 'PETtrace' centres. Ensure efficient performance of, and undertake first-line maintenance of, the FDG & FEC Synthesisers, Dispensing Equipment, Hot Cells, including dose calibration, monitoring and sterility checks within the context of strict application of environmental and 'clean room' protocols. Faults Maintain records of faults on any dysfunction - operational, equipment or environment integrity. Interpret and rectify operational faults where possible and indicate where the GE engineer or contractor should be called. Quality Systems Develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for all aspects of cyclotron operations, and radiopharmaceutical production of standard PET tracers Principal Operator/Timetable On a rota basis, act as either cyclotron principal operator or as principal laboratory technician for radio-synthesis of PET tracers in accordance with a pre-determined daily timetable. Targetary Maintain routine protocols for production of standard 18F and other PET targetary in accordance with GMP guidelines. Maintenance and Engineering Services Support appropriate Maintenance/Engineering arrangements to ensure reliable delivery of critical services including air handling, chilled water, gases, electric power and security. Chemical Preparation Ordering of stock, preparation of chemicals required for routine radiochemistry production including formulation of reagents, etc and the safe disposal of waste chemicals and materials. Standard Operating Procedures Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the QP and adoption by the unit. Training Others Provide training and support for others selected as rota/backup in cyclotron operation and production of Radiopharmaceuticals. R & D Search out, promote and manage R&D initiatives that both enhance the reputation of Alliance Medical Radiopharmacy and their professional staffs as is consistent within approved budgets and grants. Skills in Radiochemistry Develop necessary skills to provide relief and rota support to radiochemical laboratory technician/s with specific reference to the functions of: Operation of cyclotron. Production of Radioisotopes Safety and Control Assume responsibility for the safe and efficient handling of all radioactive substances (solid, gas, liquid) received from the Centre's cyclotron including their synthesis, transmission, dispensing, storage, containerisation, packing, despatch, transport, decay control, and release. In accordance with local rules for emergency or serious incident procedure record such events in accordance with SOPs. Responsible for following agreed safety procedures to ensure safety of yourself and others. Regulatory Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules developed by Alliance Medical Radiopharmacy in conformity to such licensing requirement. Alliance Medical Values Alliance Medical Values: Leaders, managers, and supervisors have a particular responsibility to be role models in terms of how they demonstrate these values themselves and how they engage their teams to work in this way. Collaboration: We work together and in partnership for all our patients. We respect expertise and combine it to achieve more. Excellence: We never compromise. We strive to deliver the very best in everything we do to ensure the highest quality of care. We treat our patients and each other with compassion, dignity and respect. Learning: Knowledge and understanding comes from learning. At Alliance Medical we are committed to ensuring that each and every one of us keeps on learning and that we continuously look for improved ways of working. Efficiency: Efficiency in healthcare means more patients get better care. We constantly seek new ways to use the scarce resource of healthcare more intelligently so that more people can live longer, fuller lives. Openness: We act with transparency and honesty in everything we do, where staff are encouraged to speak up to ensure a safe and secure environment for our patients. Additional note This Job Description is not inflexible, but is an outline and account of the main duties of the position. Any changes will be discussed with the job holder in advance. The Job Description will be reviewed periodically to take into account changes and/or developments in service requirements.
About This RoleWe have a new opportunity for a Production Radiochemist to join us at our Keele Radiopharmacy. This is a full time role working 40 hours a week attracting a salary of between £29,000 £38,000Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date.Radiochemist (Production)Main Role Undertake production of Fluorine-18 (18F) and radio-synthesis of 18F radiopharmaceuticals for PET imaging.Your place in our worldOperations Manager Production RadiochemistSkills RequiredIT SkillsDuties & ResponsibilitiesProduction Operate and maintain protocols for the manufacture of 18F and for the Alliance Medical Radiopharmacy chemistry laboratory including the production synthesis of standard 18FDG, 18Ethylcholine (18FEC), and other PET tracers in strict adherence to GMP and relevant EU pharmacopoeia standards. Operate routine protocols for customer orders and distribution of 18FDG and other PET tracers to sites. Maintenance Arrange first-line scheduled and emergency maintenance for the cyclotron and associated plant, in collaboration with GE engineers. Participate in GE training courses and maintain links with the GE Medical Systems, Sweden and other 'PETtrace' centres. Ensure efficient performance of, and undertake first-line maintenance of, the FDG & FEC Synthesisers, Dispensing Equipment, Hot Cells, including dose calibration, monitoring and sterility checks within the context of strict application of environmental and 'clean room' protocols. Faults Maintain records of faults on any dysfunction - operational, equipment or environment integrity. Interpret and rectify operational faults where possible and indicate where the GE engineer or contractor should be called. Quality Systems Develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for all aspects of cyclotron operations, and radiopharmaceutical production of standard PET tracers Principal Operator/Timetable On a rota basis, act as either cyclotron principal operator or as principal laboratory technician for radio-synthesis of PET tracers in accordance with a pre-determined daily timetable. Targetary Maintain routine protocols for production of standard 18F and other PET targetary in accordance with GMP guidelines. Maintenance and Engineering Services Support appropriate Maintenance/Engineering arrangements to ensure reliable delivery of critical services including air handling, chilled water, gases, electric power and security. Chemical Preparation Ordering of stock, preparation of chemicals required for routine radiochemistry production including formulation of reagents, etc and the safe disposal of waste chemicals and materials. Standard Operating Procedures Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the QP and adoption by the unit. Training Others Provide training and support for others selected as rota/backup in cyclotron operation and production of Radiopharmaceuticals. R & D Search out, promote and manage R& D initiatives that both enhance the reputation of Alliance Medical Radiopharmacy and their professional staffs as is consistent within approved budgets and grants. Skills in Radiochemistry Develop necessary skills to provide relief and rota support to radiochemical laboratory technician/s with specific reference to the functions of: Operation of cyclotron. Production of Radioisotopes Safety and Control Assume responsibility for the safe and efficient handling of all radioactive substances (solid, gas, liquid) received from the Centre's cyclotron including their synthesis, transmission, dispensing, storage, containerisation, packing, despatch, transport, decay control, and release. In accordance with local rules for emergency or serious incident procedure record such events in accordance with SOPs. Responsible for following agreed safety procedures to ensure safety of yourself and others. Regulatory Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules developed by Alliance Medical Radiopharmacy in conformity to such licensing requirement. Alliance Medical ValuesAlliance Medical Values: Leaders, managers, and supervisors have a particular responsibility to be role models in terms of how they demonstrate these values themselves and how they engage their teams to work in this way. Collaboration: We work together and in partnership for all our patients. We respect expertise and combine it to achieve more. Excellence: We never compromise. We strive to deliver the very best in everything we do to ensure the highest quality of care. We treat our patients and each other with compassion, dignity and respect. Learning: Knowledge and understanding comes from learning. At Alliance Medical we are committed to ensuring that each and every one of us keeps on learning and that we continuously look for improved ways of working. Efficiency: Efficiency in healthcare means more patients get better care. We constantly seek new ways to use the scarce resource of healthcare more intelligently so that more people can live longer, fuller lives. Openness: We act with transparency and honesty in everything we do, where staff are encouraged to speak up to ensure a safe and secure environment for our patients.Additional noteThis Job Description is not inflexible, but is an outline and account of the main duties of the position. Any changes will be discussed with the job holder in advance. The Job Description will be reviewed periodically to take into account changes and/or developments in service requirements.
Feb 18, 2022
Full time
About This RoleWe have a new opportunity for a Production Radiochemist to join us at our Keele Radiopharmacy. This is a full time role working 40 hours a week attracting a salary of between £29,000 £38,000Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date.Radiochemist (Production)Main Role Undertake production of Fluorine-18 (18F) and radio-synthesis of 18F radiopharmaceuticals for PET imaging.Your place in our worldOperations Manager Production RadiochemistSkills RequiredIT SkillsDuties & ResponsibilitiesProduction Operate and maintain protocols for the manufacture of 18F and for the Alliance Medical Radiopharmacy chemistry laboratory including the production synthesis of standard 18FDG, 18Ethylcholine (18FEC), and other PET tracers in strict adherence to GMP and relevant EU pharmacopoeia standards. Operate routine protocols for customer orders and distribution of 18FDG and other PET tracers to sites. Maintenance Arrange first-line scheduled and emergency maintenance for the cyclotron and associated plant, in collaboration with GE engineers. Participate in GE training courses and maintain links with the GE Medical Systems, Sweden and other 'PETtrace' centres. Ensure efficient performance of, and undertake first-line maintenance of, the FDG & FEC Synthesisers, Dispensing Equipment, Hot Cells, including dose calibration, monitoring and sterility checks within the context of strict application of environmental and 'clean room' protocols. Faults Maintain records of faults on any dysfunction - operational, equipment or environment integrity. Interpret and rectify operational faults where possible and indicate where the GE engineer or contractor should be called. Quality Systems Develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for all aspects of cyclotron operations, and radiopharmaceutical production of standard PET tracers Principal Operator/Timetable On a rota basis, act as either cyclotron principal operator or as principal laboratory technician for radio-synthesis of PET tracers in accordance with a pre-determined daily timetable. Targetary Maintain routine protocols for production of standard 18F and other PET targetary in accordance with GMP guidelines. Maintenance and Engineering Services Support appropriate Maintenance/Engineering arrangements to ensure reliable delivery of critical services including air handling, chilled water, gases, electric power and security. Chemical Preparation Ordering of stock, preparation of chemicals required for routine radiochemistry production including formulation of reagents, etc and the safe disposal of waste chemicals and materials. Standard Operating Procedures Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the QP and adoption by the unit. Training Others Provide training and support for others selected as rota/backup in cyclotron operation and production of Radiopharmaceuticals. R & D Search out, promote and manage R& D initiatives that both enhance the reputation of Alliance Medical Radiopharmacy and their professional staffs as is consistent within approved budgets and grants. Skills in Radiochemistry Develop necessary skills to provide relief and rota support to radiochemical laboratory technician/s with specific reference to the functions of: Operation of cyclotron. Production of Radioisotopes Safety and Control Assume responsibility for the safe and efficient handling of all radioactive substances (solid, gas, liquid) received from the Centre's cyclotron including their synthesis, transmission, dispensing, storage, containerisation, packing, despatch, transport, decay control, and release. In accordance with local rules for emergency or serious incident procedure record such events in accordance with SOPs. Responsible for following agreed safety procedures to ensure safety of yourself and others. Regulatory Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules developed by Alliance Medical Radiopharmacy in conformity to such licensing requirement. Alliance Medical ValuesAlliance Medical Values: Leaders, managers, and supervisors have a particular responsibility to be role models in terms of how they demonstrate these values themselves and how they engage their teams to work in this way. Collaboration: We work together and in partnership for all our patients. We respect expertise and combine it to achieve more. Excellence: We never compromise. We strive to deliver the very best in everything we do to ensure the highest quality of care. We treat our patients and each other with compassion, dignity and respect. Learning: Knowledge and understanding comes from learning. At Alliance Medical we are committed to ensuring that each and every one of us keeps on learning and that we continuously look for improved ways of working. Efficiency: Efficiency in healthcare means more patients get better care. We constantly seek new ways to use the scarce resource of healthcare more intelligently so that more people can live longer, fuller lives. Openness: We act with transparency and honesty in everything we do, where staff are encouraged to speak up to ensure a safe and secure environment for our patients.Additional noteThis Job Description is not inflexible, but is an outline and account of the main duties of the position. Any changes will be discussed with the job holder in advance. The Job Description will be reviewed periodically to take into account changes and/or developments in service requirements.
About This Role We have a new opportunity for a Quality Control Radiochemist to join our Radiopharmacy site in Sutton. This is a full time position working 40 hours a week with a salary of between £31,000 - £40,000 (dependant on experience). Ideally you should be a scientific graduate with an Analytical Chemistry background, ideally with experience of (radio) pharmaceutical QC in a GMP environment. Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date. Radiochemist (Quality Control) Main Role Undertake the quality control operations to be carried out in respect of each batch of PET radiopharmaceuticals prior to release for patient use. Duties & Responsibilities QC routines Operate and maintain routine protocols for the Erigal chemistry laboratory including the production of standard 18FDG synthesis and other PET tracers in strict adherence to GMP and relevant EU pharmacopoeia standards. Manage raw material sampling, testing and release system. Maintenance Ensure efficient performance of, and undertake first-line maintenance of, Quality Control equipment including HPLC (radiochemical and chemical purity of 18F FDG), Gas Chromatography, pH measurement, Osmolality and LAL. Faults Maintain records of faults on any dysfunction - operational or equipment. Quality Systems In association with the QP to develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for standard PET tracers. Timetable Undertake function no.1 above in accordance with a pre-determined daily timetable. Materials Ordering of chemicals, glassware, cleaning and other consumables for routine QC analysis. Formulation of reagents for radiochemistry, mixing of solvents for HPLC and other analyses, cleaning of glassware and disposal of waste chemicals and materials. Standard Operating Procedures Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the QP and adoption by the unit. Training Others Provide training and support for others selected as rota / backup in undertaking routine QC operations. R & D Search out, promote and manage R& D initiatives that both enhance the reputation of Erigal and their professional staffs as is consistent within approved budgets and grants. Skills in Radiochemistry Develop necessary skills to advise and support radiochemical laboratory technician/s with specific reference to the functions of Synthesis and Dispensing of radiotracers. Maintain understanding of best practice and changes in requirements for QC analytical testing. Safety and Control Assume responsibility for the safe and efficient handling of all radioactive sample substances (solid, gas, liquid) received from the Hot Cells room for QC tests including their movement, storage, containerisation and decay control. In accordance with local rules for emergency or serious incident procedure record such events in accordance with SOPs. Responsible for following agreed safety procedures to ensure safety of yourself and others. Regulatory Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules developed by Erigal in conformity to such licensing requirement. Alliance Medical Values Alliance Medical Values: Leaders, managers, and supervisors have a particular responsibility to be role models in terms of how they demonstrate these values themselves and how they engage their teams to work in this way. Collaboration: We work together and in partnership for all our patients. We respect expertise and combine it to achieve more. Excellence: We never compromise. We strive to deliver the very best in everything we do to ensure the highest quality of care. We treat our patients and each other with compassion, dignity and respect. Learning: Knowledge and understanding comes from learning. At Alliance Medical we are committed to ensuring that each and every one of us keeps on learning and that we continuously look for improved ways of working. Efficiency: Efficiency in healthcare means more patients get better care. We constantly seek new ways to use the scarce resource of healthcare more intelligently so that more people can live longer, fuller lives. Openness: We act with transparency and honesty in everything we do, where staff are encouraged to speak up to ensure a safe and secure environment for our patients. Additional note This Job Description is not inflexible, but is an outline and account of the main duties of the position. Any changes will be discussed with the job holder in advance. The Job Description will be reviewed periodically to take into account changes and/or developments in service requirements.
Dec 08, 2021
Full time
About This Role We have a new opportunity for a Quality Control Radiochemist to join our Radiopharmacy site in Sutton. This is a full time position working 40 hours a week with a salary of between £31,000 - £40,000 (dependant on experience). Ideally you should be a scientific graduate with an Analytical Chemistry background, ideally with experience of (radio) pharmaceutical QC in a GMP environment. Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date. Radiochemist (Quality Control) Main Role Undertake the quality control operations to be carried out in respect of each batch of PET radiopharmaceuticals prior to release for patient use. Duties & Responsibilities QC routines Operate and maintain routine protocols for the Erigal chemistry laboratory including the production of standard 18FDG synthesis and other PET tracers in strict adherence to GMP and relevant EU pharmacopoeia standards. Manage raw material sampling, testing and release system. Maintenance Ensure efficient performance of, and undertake first-line maintenance of, Quality Control equipment including HPLC (radiochemical and chemical purity of 18F FDG), Gas Chromatography, pH measurement, Osmolality and LAL. Faults Maintain records of faults on any dysfunction - operational or equipment. Quality Systems In association with the QP to develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for standard PET tracers. Timetable Undertake function no.1 above in accordance with a pre-determined daily timetable. Materials Ordering of chemicals, glassware, cleaning and other consumables for routine QC analysis. Formulation of reagents for radiochemistry, mixing of solvents for HPLC and other analyses, cleaning of glassware and disposal of waste chemicals and materials. Standard Operating Procedures Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the QP and adoption by the unit. Training Others Provide training and support for others selected as rota / backup in undertaking routine QC operations. R & D Search out, promote and manage R& D initiatives that both enhance the reputation of Erigal and their professional staffs as is consistent within approved budgets and grants. Skills in Radiochemistry Develop necessary skills to advise and support radiochemical laboratory technician/s with specific reference to the functions of Synthesis and Dispensing of radiotracers. Maintain understanding of best practice and changes in requirements for QC analytical testing. Safety and Control Assume responsibility for the safe and efficient handling of all radioactive sample substances (solid, gas, liquid) received from the Hot Cells room for QC tests including their movement, storage, containerisation and decay control. In accordance with local rules for emergency or serious incident procedure record such events in accordance with SOPs. Responsible for following agreed safety procedures to ensure safety of yourself and others. Regulatory Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules developed by Erigal in conformity to such licensing requirement. Alliance Medical Values Alliance Medical Values: Leaders, managers, and supervisors have a particular responsibility to be role models in terms of how they demonstrate these values themselves and how they engage their teams to work in this way. Collaboration: We work together and in partnership for all our patients. We respect expertise and combine it to achieve more. Excellence: We never compromise. We strive to deliver the very best in everything we do to ensure the highest quality of care. We treat our patients and each other with compassion, dignity and respect. Learning: Knowledge and understanding comes from learning. At Alliance Medical we are committed to ensuring that each and every one of us keeps on learning and that we continuously look for improved ways of working. Efficiency: Efficiency in healthcare means more patients get better care. We constantly seek new ways to use the scarce resource of healthcare more intelligently so that more people can live longer, fuller lives. Openness: We act with transparency and honesty in everything we do, where staff are encouraged to speak up to ensure a safe and secure environment for our patients. Additional note This Job Description is not inflexible, but is an outline and account of the main duties of the position. Any changes will be discussed with the job holder in advance. The Job Description will be reviewed periodically to take into account changes and/or developments in service requirements.
About This Role We have an exciting opportunity for a Production Radiochemist to join us on a 12 month Fixed Term Contract at our Guildford Radiopharmacy. We also have a second vacancy for a Production Radiochemist on a permanent contract. Please state in your application if you are interested in the Fixed Term or Permanent position. These are full time positions working 40 hours a week (Monday-Sunday) with a salary circa £31,000. Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date. Radiochemist (Production) Main Role Undertake production of Fluorine-18 (18F) and radio-synthesis of 18F radiopharmaceuticals for PET imaging. Duties & Responsibilities Production Operate and maintain protocols for the manufacture of 18F and for the Alliance Medical Radiopharmacy chemistry laboratory including the production synthesis of standard 18FDG, 18Ethylcholine (18FEC), and other PET tracers in strict adherence to GMP and relevant EU pharmacopoeia standards. Operate routine protocols for customer orders and distribution of 18FDG and other PET tracers to sites. Maintenance Arrange first-line scheduled and emergency maintenance for the cyclotron and associated plant, in collaboration with GE engineers. Participate in GE training courses and maintain links with the GE Medical Systems, Sweden and other 'PETtrace' centres. Ensure efficient performance of, and undertake first-line maintenance of, the FDG & FEC Synthesisers, Dispensing Equipment, Hot Cells, including dose calibration, monitoring and sterility checks within the context of strict application of environmental and 'clean room' protocols. Faults Maintain records of faults on any dysfunction - operational, equipment or environment integrity. Interpret and rectify operational faults where possible and indicate where the GE engineer or contractor should be called. Quality Systems Develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for all aspects of cyclotron operations, and radiopharmaceutical production of standard PET tracers Principal Operator/Timetable On a rota basis, act as either cyclotron principal operator or as principal laboratory technician for radio-synthesis of PET tracers in accordance with a pre-determined daily timetable. Targetary Maintain routine protocols for production of standard 18F and other PET targetary in accordance with GMP guidelines. Maintenance and Engineering Services Support appropriate Maintenance/Engineering arrangements to ensure reliable delivery of critical services including air handling, chilled water, gases, electric power and security. Chemical Preparation Ordering of stock, preparation of chemicals required for routine radiochemistry production including formulation of reagents, etc and the safe disposal of waste chemicals and materials. Standard Operating Procedures Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the QP and adoption by the unit. Training Others Provide training and support for others selected as rota/backup in cyclotron operation and production of Radiopharmaceuticals. R & D Search out, promote and manage R&D initiatives that both enhance the reputation of Alliance Medical Radiopharmacy and their professional staffs as is consistent within approved budgets and grants. Skills in Radiochemistry Develop necessary skills to provide relief and rota support to radiochemical laboratory technician/s with specific reference to the functions of: Operation of cyclotron. Production of Radioisotopes Safety and Control Assume responsibility for the safe and efficient handling of all radioactive substances (solid, gas, liquid) received from the Centre's cyclotron including their synthesis, transmission, dispensing, storage, containerisation, packing, despatch, transport, decay control, and release. In accordance with local rules for emergency or serious incident procedure record such events in accordance with SOPs. Responsible for following agreed safety procedures to ensure safety of yourself and others. Regulatory Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules developed by Alliance Medical Radiopharmacy in conformity to such licensing requirement. Alliance Medical Values Alliance Medical Values: Leaders, managers, and supervisors have a particular responsibility to be role models in terms of how they demonstrate these values themselves and how they engage their teams to work in this way. Collaboration: We work together and in partnership for all our patients. We respect expertise and combine it to achieve more. Excellence: We never compromise. We strive to deliver the very best in everything we do to ensure the highest quality of care. We treat our patients and each other with compassion, dignity and respect. Learning: Knowledge and understanding comes from learning. At Alliance Medical we are committed to ensuring that each and every one of us keeps on learning and that we continuously look for improved ways of working. Efficiency: Efficiency in healthcare means more patients get better care. We constantly seek new ways to use the scarce resource of healthcare more intelligently so that more people can live longer, fuller lives. Openness: We act with transparency and honesty in everything we do, where staff are encouraged to speak up to ensure a safe and secure environment for our patients. Additional note This Job Description is not inflexible, but is an outline and account of the main duties of the position. Any changes will be discussed with the job holder in advance. The Job Description will be reviewed periodically to take into account changes and/or developments in service requirements.
Dec 07, 2021
Full time
About This Role We have an exciting opportunity for a Production Radiochemist to join us on a 12 month Fixed Term Contract at our Guildford Radiopharmacy. We also have a second vacancy for a Production Radiochemist on a permanent contract. Please state in your application if you are interested in the Fixed Term or Permanent position. These are full time positions working 40 hours a week (Monday-Sunday) with a salary circa £31,000. Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date. Radiochemist (Production) Main Role Undertake production of Fluorine-18 (18F) and radio-synthesis of 18F radiopharmaceuticals for PET imaging. Duties & Responsibilities Production Operate and maintain protocols for the manufacture of 18F and for the Alliance Medical Radiopharmacy chemistry laboratory including the production synthesis of standard 18FDG, 18Ethylcholine (18FEC), and other PET tracers in strict adherence to GMP and relevant EU pharmacopoeia standards. Operate routine protocols for customer orders and distribution of 18FDG and other PET tracers to sites. Maintenance Arrange first-line scheduled and emergency maintenance for the cyclotron and associated plant, in collaboration with GE engineers. Participate in GE training courses and maintain links with the GE Medical Systems, Sweden and other 'PETtrace' centres. Ensure efficient performance of, and undertake first-line maintenance of, the FDG & FEC Synthesisers, Dispensing Equipment, Hot Cells, including dose calibration, monitoring and sterility checks within the context of strict application of environmental and 'clean room' protocols. Faults Maintain records of faults on any dysfunction - operational, equipment or environment integrity. Interpret and rectify operational faults where possible and indicate where the GE engineer or contractor should be called. Quality Systems Develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for all aspects of cyclotron operations, and radiopharmaceutical production of standard PET tracers Principal Operator/Timetable On a rota basis, act as either cyclotron principal operator or as principal laboratory technician for radio-synthesis of PET tracers in accordance with a pre-determined daily timetable. Targetary Maintain routine protocols for production of standard 18F and other PET targetary in accordance with GMP guidelines. Maintenance and Engineering Services Support appropriate Maintenance/Engineering arrangements to ensure reliable delivery of critical services including air handling, chilled water, gases, electric power and security. Chemical Preparation Ordering of stock, preparation of chemicals required for routine radiochemistry production including formulation of reagents, etc and the safe disposal of waste chemicals and materials. Standard Operating Procedures Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the QP and adoption by the unit. Training Others Provide training and support for others selected as rota/backup in cyclotron operation and production of Radiopharmaceuticals. R & D Search out, promote and manage R&D initiatives that both enhance the reputation of Alliance Medical Radiopharmacy and their professional staffs as is consistent within approved budgets and grants. Skills in Radiochemistry Develop necessary skills to provide relief and rota support to radiochemical laboratory technician/s with specific reference to the functions of: Operation of cyclotron. Production of Radioisotopes Safety and Control Assume responsibility for the safe and efficient handling of all radioactive substances (solid, gas, liquid) received from the Centre's cyclotron including their synthesis, transmission, dispensing, storage, containerisation, packing, despatch, transport, decay control, and release. In accordance with local rules for emergency or serious incident procedure record such events in accordance with SOPs. Responsible for following agreed safety procedures to ensure safety of yourself and others. Regulatory Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules developed by Alliance Medical Radiopharmacy in conformity to such licensing requirement. Alliance Medical Values Alliance Medical Values: Leaders, managers, and supervisors have a particular responsibility to be role models in terms of how they demonstrate these values themselves and how they engage their teams to work in this way. Collaboration: We work together and in partnership for all our patients. We respect expertise and combine it to achieve more. Excellence: We never compromise. We strive to deliver the very best in everything we do to ensure the highest quality of care. We treat our patients and each other with compassion, dignity and respect. Learning: Knowledge and understanding comes from learning. At Alliance Medical we are committed to ensuring that each and every one of us keeps on learning and that we continuously look for improved ways of working. Efficiency: Efficiency in healthcare means more patients get better care. We constantly seek new ways to use the scarce resource of healthcare more intelligently so that more people can live longer, fuller lives. Openness: We act with transparency and honesty in everything we do, where staff are encouraged to speak up to ensure a safe and secure environment for our patients. Additional note This Job Description is not inflexible, but is an outline and account of the main duties of the position. Any changes will be discussed with the job holder in advance. The Job Description will be reviewed periodically to take into account changes and/or developments in service requirements.
Leading international Pharmaceutical Manufacturer seeks a Microbiology Laboratory Technician on a 9 month FTC. About the role: To carry out environmental monitoring (EM) program of aseptic compounding centre including; taking daily samples within production cleanroom areas, incubation, plate reading and identification of isolates...... click apply for full job details
Dec 05, 2021
Contractor
Leading international Pharmaceutical Manufacturer seeks a Microbiology Laboratory Technician on a 9 month FTC. About the role: To carry out environmental monitoring (EM) program of aseptic compounding centre including; taking daily samples within production cleanroom areas, incubation, plate reading and identification of isolates...... click apply for full job details
About This Role We have a new opportunity for a Production Radiochemist to join us at our Preston Radiopharmacy Site. This is a full time, permanent position attracting a salary of £29,000. Ideally you should be a scientific graduate with a scientific background, ideally with experience of (radio) pharmaceutical manufacture in a GMP environment. Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date. Radiochemist (Production) Main Role Undertake production of Fluorine-18 (18F) and radio-synthesis of 18F radiopharmaceuticals for PET imaging. Duties & Responsibilities Production Operate and maintain protocols for the manufacture of 18F and for the Alliance Medical Radiopharmacy chemistry laboratory including the production synthesis of standard 18FDG, 18Ethylcholine (18FEC), and other PET tracers in strict adherence to GMP and relevant EU pharmacopoeia standards. Operate routine protocols for customer orders and distribution of 18FDG and other PET tracers to sites. Maintenance Arrange first-line scheduled and emergency maintenance for the cyclotron and associated plant, in collaboration with GE engineers. Participate in GE training courses and maintain links with the GE Medical Systems, Sweden and other 'PETtrace' centres. Ensure efficient performance of, and undertake first-line maintenance of, the FDG & FEC Synthesisers, Dispensing Equipment, Hot Cells, including dose calibration, monitoring and sterility checks within the context of strict application of environmental and 'clean room' protocols. Faults Maintain records of faults on any dysfunction - operational, equipment or environment integrity. Interpret and rectify operational faults where possible and indicate where the GE engineer or contractor should be called. Quality Systems Develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for all aspects of cyclotron operations, and radiopharmaceutical production of standard PET tracers Principal Operator/Timetable On a rota basis, act as either cyclotron principal operator or as principal laboratory technician for radio-synthesis of PET tracers in accordance with a pre-determined daily timetable. Targetary Maintain routine protocols for production of standard 18F and other PET targetary in accordance with GMP guidelines. Maintenance and Engineering Services Support appropriate Maintenance/Engineering arrangements to ensure reliable delivery of critical services including air handling, chilled water, gases, electric power and security. Chemical Preparation Ordering of stock, preparation of chemicals required for routine radiochemistry production including formulation of reagents, etc and the safe disposal of waste chemicals and materials. Standard Operating Procedures Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the QP and adoption by the unit. Training Others Provide training and support for others selected as rota/backup in cyclotron operation and production of Radiopharmaceuticals. R & D Search out, promote and manage R&D initiatives that both enhance the reputation of Alliance Medical Radiopharmacy and their professional staffs as is consistent within approved budgets and grants. Skills in Radiochemistry Develop necessary skills to provide relief and rota support to radiochemical laboratory technician/s with specific reference to the functions of: Operation of cyclotron. Production of Radioisotopes Safety and Control Assume responsibility for the safe and efficient handling of all radioactive substances (solid, gas, liquid) received from the Centre's cyclotron including their synthesis, transmission, dispensing, storage, containerisation, packing, despatch, transport, decay control, and release. In accordance with local rules for emergency or serious incident procedure record such events in accordance with SOPs. Responsible for following agreed safety procedures to ensure safety of yourself and others. Regulatory Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules developed by Alliance Medical Radiopharmacy in conformity to such licensing requirement. Alliance Medical Values Alliance Medical Values: Leaders, managers, and supervisors have a particular responsibility to be role models in terms of how they demonstrate these values themselves and how they engage their teams to work in this way. Collaboration: We work together and in partnership for all our patients. We respect expertise and combine it to achieve more. Excellence: We never compromise. We strive to deliver the very best in everything we do to ensure the highest quality of care. We treat our patients and each other with compassion, dignity and respect. Learning: Knowledge and understanding comes from learning. At Alliance Medical we are committed to ensuring that each and every one of us keeps on learning and that we continuously look for improved ways of working. Efficiency: Efficiency in healthcare means more patients get better care. We constantly seek new ways to use the scarce resource of healthcare more intelligently so that more people can live longer, fuller lives. Openness: We act with transparency and honesty in everything we do, where staff are encouraged to speak up to ensure a safe and secure environment for our patients. Additional note This Job Description is not inflexible, but is an outline and account of the main duties of the position. Any changes will be discussed with the job holder in advance. The Job Description will be reviewed periodically to take into account changes and/or developments in service requirements.
Dec 01, 2021
Full time
About This Role We have a new opportunity for a Production Radiochemist to join us at our Preston Radiopharmacy Site. This is a full time, permanent position attracting a salary of £29,000. Ideally you should be a scientific graduate with a scientific background, ideally with experience of (radio) pharmaceutical manufacture in a GMP environment. Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date. Radiochemist (Production) Main Role Undertake production of Fluorine-18 (18F) and radio-synthesis of 18F radiopharmaceuticals for PET imaging. Duties & Responsibilities Production Operate and maintain protocols for the manufacture of 18F and for the Alliance Medical Radiopharmacy chemistry laboratory including the production synthesis of standard 18FDG, 18Ethylcholine (18FEC), and other PET tracers in strict adherence to GMP and relevant EU pharmacopoeia standards. Operate routine protocols for customer orders and distribution of 18FDG and other PET tracers to sites. Maintenance Arrange first-line scheduled and emergency maintenance for the cyclotron and associated plant, in collaboration with GE engineers. Participate in GE training courses and maintain links with the GE Medical Systems, Sweden and other 'PETtrace' centres. Ensure efficient performance of, and undertake first-line maintenance of, the FDG & FEC Synthesisers, Dispensing Equipment, Hot Cells, including dose calibration, monitoring and sterility checks within the context of strict application of environmental and 'clean room' protocols. Faults Maintain records of faults on any dysfunction - operational, equipment or environment integrity. Interpret and rectify operational faults where possible and indicate where the GE engineer or contractor should be called. Quality Systems Develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for all aspects of cyclotron operations, and radiopharmaceutical production of standard PET tracers Principal Operator/Timetable On a rota basis, act as either cyclotron principal operator or as principal laboratory technician for radio-synthesis of PET tracers in accordance with a pre-determined daily timetable. Targetary Maintain routine protocols for production of standard 18F and other PET targetary in accordance with GMP guidelines. Maintenance and Engineering Services Support appropriate Maintenance/Engineering arrangements to ensure reliable delivery of critical services including air handling, chilled water, gases, electric power and security. Chemical Preparation Ordering of stock, preparation of chemicals required for routine radiochemistry production including formulation of reagents, etc and the safe disposal of waste chemicals and materials. Standard Operating Procedures Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the QP and adoption by the unit. Training Others Provide training and support for others selected as rota/backup in cyclotron operation and production of Radiopharmaceuticals. R & D Search out, promote and manage R&D initiatives that both enhance the reputation of Alliance Medical Radiopharmacy and their professional staffs as is consistent within approved budgets and grants. Skills in Radiochemistry Develop necessary skills to provide relief and rota support to radiochemical laboratory technician/s with specific reference to the functions of: Operation of cyclotron. Production of Radioisotopes Safety and Control Assume responsibility for the safe and efficient handling of all radioactive substances (solid, gas, liquid) received from the Centre's cyclotron including their synthesis, transmission, dispensing, storage, containerisation, packing, despatch, transport, decay control, and release. In accordance with local rules for emergency or serious incident procedure record such events in accordance with SOPs. Responsible for following agreed safety procedures to ensure safety of yourself and others. Regulatory Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules developed by Alliance Medical Radiopharmacy in conformity to such licensing requirement. Alliance Medical Values Alliance Medical Values: Leaders, managers, and supervisors have a particular responsibility to be role models in terms of how they demonstrate these values themselves and how they engage their teams to work in this way. Collaboration: We work together and in partnership for all our patients. We respect expertise and combine it to achieve more. Excellence: We never compromise. We strive to deliver the very best in everything we do to ensure the highest quality of care. We treat our patients and each other with compassion, dignity and respect. Learning: Knowledge and understanding comes from learning. At Alliance Medical we are committed to ensuring that each and every one of us keeps on learning and that we continuously look for improved ways of working. Efficiency: Efficiency in healthcare means more patients get better care. We constantly seek new ways to use the scarce resource of healthcare more intelligently so that more people can live longer, fuller lives. Openness: We act with transparency and honesty in everything we do, where staff are encouraged to speak up to ensure a safe and secure environment for our patients. Additional note This Job Description is not inflexible, but is an outline and account of the main duties of the position. Any changes will be discussed with the job holder in advance. The Job Description will be reviewed periodically to take into account changes and/or developments in service requirements.
About This Role We have a new opportunity for a Production Radiochemist to join us at our Sutton Radiopharmacy Site. This is a full time position working 40 hours a week attracting a salary of £31,000. Ideally you are a scientific graduate with a scientific background, ideally with experience of (radio) pharmaceutical manufacture in a GMP environment. Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date. Radiochemist (Production) Main Role Undertake production of Fluorine-18 (18F) and radio-synthesis of 18F radiopharmaceuticals for PET imaging. Duties & Responsibilities Production Operate and maintain protocols for the manufacture of 18F and for the Alliance Medical Radiopharmacy chemistry laboratory including the production synthesis of standard 18FDG, 18Ethylcholine (18FEC), and other PET tracers in strict adherence to GMP and relevant EU pharmacopoeia standards. Operate routine protocols for customer orders and distribution of 18FDG and other PET tracers to sites. Maintenance Arrange first-line scheduled and emergency maintenance for the cyclotron and associated plant, in collaboration with GE engineers. Participate in GE training courses and maintain links with the GE Medical Systems, Sweden and other 'PETtrace' centres. Ensure efficient performance of, and undertake first-line maintenance of, the FDG & FEC Synthesisers, Dispensing Equipment, Hot Cells, including dose calibration, monitoring and sterility checks within the context of strict application of environmental and 'clean room' protocols. Faults Maintain records of faults on any dysfunction - operational, equipment or environment integrity. Interpret and rectify operational faults where possible and indicate where the GE engineer or contractor should be called. Quality Systems Develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for all aspects of cyclotron operations, and radiopharmaceutical production of standard PET tracers Principal Operator/Timetable On a rota basis, act as either cyclotron principal operator or as principal laboratory technician for radio-synthesis of PET tracers in accordance with a pre-determined daily timetable. Targetary Maintain routine protocols for production of standard 18F and other PET targetary in accordance with GMP guidelines. Maintenance and Engineering Services Support appropriate Maintenance/Engineering arrangements to ensure reliable delivery of critical services including air handling, chilled water, gases, electric power and security. Chemical Preparation Ordering of stock, preparation of chemicals required for routine radiochemistry production including formulation of reagents, etc and the safe disposal of waste chemicals and materials. Standard Operating Procedures Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the QP and adoption by the unit. Training Others Provide training and support for others selected as rota/backup in cyclotron operation and production of Radiopharmaceuticals. R & D Search out, promote and manage R&D initiatives that both enhance the reputation of Alliance Medical Radiopharmacy and their professional staffs as is consistent within approved budgets and grants. Skills in Radiochemistry Develop necessary skills to provide relief and rota support to radiochemical laboratory technician/s with specific reference to the functions of: Operation of cyclotron. Production of Radioisotopes Safety and Control Assume responsibility for the safe and efficient handling of all radioactive substances (solid, gas, liquid) received from the Centre's cyclotron including their synthesis, transmission, dispensing, storage, containerisation, packing, despatch, transport, decay control, and release. In accordance with local rules for emergency or serious incident procedure record such events in accordance with SOPs. Responsible for following agreed safety procedures to ensure safety of yourself and others. Regulatory Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules developed by Alliance Medical Radiopharmacy in conformity to such licensing requirement. Alliance Medical Values Alliance Medical Values: Leaders, managers, and supervisors have a particular responsibility to be role models in terms of how they demonstrate these values themselves and how they engage their teams to work in this way. Collaboration: We work together and in partnership for all our patients. We respect expertise and combine it to achieve more. Excellence: We never compromise. We strive to deliver the very best in everything we do to ensure the highest quality of care. We treat our patients and each other with compassion, dignity and respect. Learning: Knowledge and understanding comes from learning. At Alliance Medical we are committed to ensuring that each and every one of us keeps on learning and that we continuously look for improved ways of working. Efficiency: Efficiency in healthcare means more patients get better care. We constantly seek new ways to use the scarce resource of healthcare more intelligently so that more people can live longer, fuller lives. Openness: We act with transparency and honesty in everything we do, where staff are encouraged to speak up to ensure a safe and secure environment for our patients. Additional note This Job Description is not inflexible, but is an outline and account of the main duties of the position. Any changes will be discussed with the job holder in advance. The Job Description will be reviewed periodically to take into account changes and/or developments in service requirements.
Dec 01, 2021
Full time
About This Role We have a new opportunity for a Production Radiochemist to join us at our Sutton Radiopharmacy Site. This is a full time position working 40 hours a week attracting a salary of £31,000. Ideally you are a scientific graduate with a scientific background, ideally with experience of (radio) pharmaceutical manufacture in a GMP environment. Please note that we will be interviewing throughout the duration of this advert. Therefore if you are interested in this role an early application is advised as we may close the advert prior to the advertised date. Radiochemist (Production) Main Role Undertake production of Fluorine-18 (18F) and radio-synthesis of 18F radiopharmaceuticals for PET imaging. Duties & Responsibilities Production Operate and maintain protocols for the manufacture of 18F and for the Alliance Medical Radiopharmacy chemistry laboratory including the production synthesis of standard 18FDG, 18Ethylcholine (18FEC), and other PET tracers in strict adherence to GMP and relevant EU pharmacopoeia standards. Operate routine protocols for customer orders and distribution of 18FDG and other PET tracers to sites. Maintenance Arrange first-line scheduled and emergency maintenance for the cyclotron and associated plant, in collaboration with GE engineers. Participate in GE training courses and maintain links with the GE Medical Systems, Sweden and other 'PETtrace' centres. Ensure efficient performance of, and undertake first-line maintenance of, the FDG & FEC Synthesisers, Dispensing Equipment, Hot Cells, including dose calibration, monitoring and sterility checks within the context of strict application of environmental and 'clean room' protocols. Faults Maintain records of faults on any dysfunction - operational, equipment or environment integrity. Interpret and rectify operational faults where possible and indicate where the GE engineer or contractor should be called. Quality Systems Develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for all aspects of cyclotron operations, and radiopharmaceutical production of standard PET tracers Principal Operator/Timetable On a rota basis, act as either cyclotron principal operator or as principal laboratory technician for radio-synthesis of PET tracers in accordance with a pre-determined daily timetable. Targetary Maintain routine protocols for production of standard 18F and other PET targetary in accordance with GMP guidelines. Maintenance and Engineering Services Support appropriate Maintenance/Engineering arrangements to ensure reliable delivery of critical services including air handling, chilled water, gases, electric power and security. Chemical Preparation Ordering of stock, preparation of chemicals required for routine radiochemistry production including formulation of reagents, etc and the safe disposal of waste chemicals and materials. Standard Operating Procedures Prepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the QP and adoption by the unit. Training Others Provide training and support for others selected as rota/backup in cyclotron operation and production of Radiopharmaceuticals. R & D Search out, promote and manage R&D initiatives that both enhance the reputation of Alliance Medical Radiopharmacy and their professional staffs as is consistent within approved budgets and grants. Skills in Radiochemistry Develop necessary skills to provide relief and rota support to radiochemical laboratory technician/s with specific reference to the functions of: Operation of cyclotron. Production of Radioisotopes Safety and Control Assume responsibility for the safe and efficient handling of all radioactive substances (solid, gas, liquid) received from the Centre's cyclotron including their synthesis, transmission, dispensing, storage, containerisation, packing, despatch, transport, decay control, and release. In accordance with local rules for emergency or serious incident procedure record such events in accordance with SOPs. Responsible for following agreed safety procedures to ensure safety of yourself and others. Regulatory Strictly adhere to GMP, GLP and safety protocols laid down by the MHRA, EA and HSE in accordance with issued licenses as determined from time to time. Corresponding adherence to local rules developed by Alliance Medical Radiopharmacy in conformity to such licensing requirement. Alliance Medical Values Alliance Medical Values: Leaders, managers, and supervisors have a particular responsibility to be role models in terms of how they demonstrate these values themselves and how they engage their teams to work in this way. Collaboration: We work together and in partnership for all our patients. We respect expertise and combine it to achieve more. Excellence: We never compromise. We strive to deliver the very best in everything we do to ensure the highest quality of care. We treat our patients and each other with compassion, dignity and respect. Learning: Knowledge and understanding comes from learning. At Alliance Medical we are committed to ensuring that each and every one of us keeps on learning and that we continuously look for improved ways of working. Efficiency: Efficiency in healthcare means more patients get better care. We constantly seek new ways to use the scarce resource of healthcare more intelligently so that more people can live longer, fuller lives. Openness: We act with transparency and honesty in everything we do, where staff are encouraged to speak up to ensure a safe and secure environment for our patients. Additional note This Job Description is not inflexible, but is an outline and account of the main duties of the position. Any changes will be discussed with the job holder in advance. The Job Description will be reviewed periodically to take into account changes and/or developments in service requirements.