Trainee QC Laboratory Analyst When registering to this job board you will be redirected to the online application form. Please ensure that this is completed in full in order that your application can be reviewed. We are looking to recruit a Trainee Analystfor the 2 shift / 5 day shift pattern within the Quality Control Laboratory at our Stowmarket Site click apply for full job details
Mar 29, 2024
Full time
Trainee QC Laboratory Analyst When registering to this job board you will be redirected to the online application form. Please ensure that this is completed in full in order that your application can be reviewed. We are looking to recruit a Trainee Analystfor the 2 shift / 5 day shift pattern within the Quality Control Laboratory at our Stowmarket Site click apply for full job details
Trainee QC Laboratory Analyst When registering to this job board you will be redirected to the online application form. Please ensure that this is completed in full in order that your application can be reviewed. We are looking to recruit a Trainee Analyst for the 2 shift / 5 day shift pattern within the Quality Control Laboratory at our Stowmarket Site. This is a permanent role. Prospective candidates should have a science based education (GCSE) and an ability to carry out multiple tasks in a logical fashion. Previous laboratory experience is not essential, as full training will be given. This is a great entry level role. Principle Responsibilities: To undertake quality control analysis on liquid and dried extract, barley, malt and milled products. Follow work instructions in an organised, accurate and tidy manner in order to provide the analysis by the required time. The Candidate: A good team player and communicator. An awareness of Health & Safety principles. Self confidence and initiative to work with minimum supervision. A science/mathematics based education Hours of Work: Current requirements for this role are for 37.5 hours per week covering a 2 shift / 5 day shift pattern. Monday to Friday. Alternative 6.00 am to 2.00 pm and 1.30 pm to 9.30 pm. However, there is potential for the role to progress into a 2 shift / 7 day role. Training: We anticipate that the initial training period will be for a minimum of 3 months depending on the experience of the successful candidate. During the training period the hours of work will be Monday to Friday, 6.00 am to 2.00 pm with a 30-minute unpaid meal break.
Mar 27, 2024
Full time
Trainee QC Laboratory Analyst When registering to this job board you will be redirected to the online application form. Please ensure that this is completed in full in order that your application can be reviewed. We are looking to recruit a Trainee Analyst for the 2 shift / 5 day shift pattern within the Quality Control Laboratory at our Stowmarket Site. This is a permanent role. Prospective candidates should have a science based education (GCSE) and an ability to carry out multiple tasks in a logical fashion. Previous laboratory experience is not essential, as full training will be given. This is a great entry level role. Principle Responsibilities: To undertake quality control analysis on liquid and dried extract, barley, malt and milled products. Follow work instructions in an organised, accurate and tidy manner in order to provide the analysis by the required time. The Candidate: A good team player and communicator. An awareness of Health & Safety principles. Self confidence and initiative to work with minimum supervision. A science/mathematics based education Hours of Work: Current requirements for this role are for 37.5 hours per week covering a 2 shift / 5 day shift pattern. Monday to Friday. Alternative 6.00 am to 2.00 pm and 1.30 pm to 9.30 pm. However, there is potential for the role to progress into a 2 shift / 7 day role. Training: We anticipate that the initial training period will be for a minimum of 3 months depending on the experience of the successful candidate. During the training period the hours of work will be Monday to Friday, 6.00 am to 2.00 pm with a 30-minute unpaid meal break.
Organic Analyst & Senior Analyst, GC/MS Location: Cambridge Salary:£26,000 - £28,000 Dependant on experience Role: Conducting regular/ daily GC test work (GC FID & GC/MS), whilst maintaining and calibrating the instruments. Assistance in the generation of accurate and timely sample and QC data in line with client expectations and our clients Quality Systems click apply for full job details
Mar 27, 2024
Full time
Organic Analyst & Senior Analyst, GC/MS Location: Cambridge Salary:£26,000 - £28,000 Dependant on experience Role: Conducting regular/ daily GC test work (GC FID & GC/MS), whilst maintaining and calibrating the instruments. Assistance in the generation of accurate and timely sample and QC data in line with client expectations and our clients Quality Systems click apply for full job details
AML/CDD Analyst required for a leading professional service firm based in Southampton. You will focus on CDD, client outreach, updating the company data management systems and conducting QC, plus lots more. The role covers the following: Liaising with members of the firm and clients to obtain refreshed CDD documentation as required Undertaking open-source searches via independent intelligence databases Updating the company data management systems accurately to allow for ongoing sanctions screening Ensuring that the electronic filing system is maintained correctly, including maintaining the central database for the storing of CDD and assessing client risk and escalating to senior compliance and management, where necessary Assistance with onboarding may also be required If you are interested in this opportunity and would like to apply, please submit your CV. Please note, should feedback not be received within 28 days due to the large volume of applications, unfortunately, your application has been unsuccessful. However, I may be in touch with similar relevant opportunities.
Mar 25, 2024
Full time
AML/CDD Analyst required for a leading professional service firm based in Southampton. You will focus on CDD, client outreach, updating the company data management systems and conducting QC, plus lots more. The role covers the following: Liaising with members of the firm and clients to obtain refreshed CDD documentation as required Undertaking open-source searches via independent intelligence databases Updating the company data management systems accurately to allow for ongoing sanctions screening Ensuring that the electronic filing system is maintained correctly, including maintaining the central database for the storing of CDD and assessing client risk and escalating to senior compliance and management, where necessary Assistance with onboarding may also be required If you are interested in this opportunity and would like to apply, please submit your CV. Please note, should feedback not be received within 28 days due to the large volume of applications, unfortunately, your application has been unsuccessful. However, I may be in touch with similar relevant opportunities.
Job: Assistant Risk Analyst Location: London Job Type: Permanent Job Description The Assistant Risk Analyst supports the Risk Lead to drive best practice risk management and help provide data-driven insights to minimise the impacted value of risks through measuring mitigations and highlighting common themes across risk/high risk areas to drive and account for suitable contingency levels. Responsibilities Support the identification and mitigation of (threats and opportunity) through regular risk workshops. Support contractors and the internal organisation understanding on risk management practices. Help implement mitigation actions against associated risks across projects and programmes ensuring they are carried out as per agreed dates Maintain visibility of threat/opportunity trigger points to facilitate risk cost profiling, draw down of risk budget or retirement of risks. Support projects in improving their risk management skills and maturity. Assist with risk analysis, insight, and reporting around project and programme level risk Work across Capital programme to develop and share risk management best practice. You will learn to guide Capital programme through the risk management process. You will become an expert, providing advice and hands-on training to help them become better at managing risks. Support risk reviews to identify important themes across the Capital programme and guide best practice mitigations. Promote the need and implementation of mitigation actions against associated risks across projects and programmes. (SMART) which drive the impact of risk Maintain visibility of threat/opportunity P6 link to facilitate risk cost profiling, retirement of risks. Produce risk reports promptly to help communicate threat and opportunity status Qualifications Understanding of the main principles are QCRA/QSRA desirable. Previous experience in a project risk management setting desirable but not essential APM PMQ/IRM/Axelos Risk management qualifications advantageous
Mar 25, 2024
Full time
Job: Assistant Risk Analyst Location: London Job Type: Permanent Job Description The Assistant Risk Analyst supports the Risk Lead to drive best practice risk management and help provide data-driven insights to minimise the impacted value of risks through measuring mitigations and highlighting common themes across risk/high risk areas to drive and account for suitable contingency levels. Responsibilities Support the identification and mitigation of (threats and opportunity) through regular risk workshops. Support contractors and the internal organisation understanding on risk management practices. Help implement mitigation actions against associated risks across projects and programmes ensuring they are carried out as per agreed dates Maintain visibility of threat/opportunity trigger points to facilitate risk cost profiling, draw down of risk budget or retirement of risks. Support projects in improving their risk management skills and maturity. Assist with risk analysis, insight, and reporting around project and programme level risk Work across Capital programme to develop and share risk management best practice. You will learn to guide Capital programme through the risk management process. You will become an expert, providing advice and hands-on training to help them become better at managing risks. Support risk reviews to identify important themes across the Capital programme and guide best practice mitigations. Promote the need and implementation of mitigation actions against associated risks across projects and programmes. (SMART) which drive the impact of risk Maintain visibility of threat/opportunity P6 link to facilitate risk cost profiling, retirement of risks. Produce risk reports promptly to help communicate threat and opportunity status Qualifications Understanding of the main principles are QCRA/QSRA desirable. Previous experience in a project risk management setting desirable but not essential APM PMQ/IRM/Axelos Risk management qualifications advantageous
Territory: Midland's region with national travel as required and travel to clients in the Nordic region (Norway, Sweden, Denmark, Finland areas) circa 1 week every two months Your Location: Living anywhere on territory in the Midlands i.e., Birmingham, Coventry, Leicester, Derby, Nottingham, Lincoln, Northampton areas Do you want to work for a global leader in the development and manufacture of cutting-edge semi & fully automated pharmaceutical dissolution tablet testing technology?! Are you already a Field Service Engineer with 2+ years of experience installing, validating, and servicing pharmaceutical dissolution/tablet testing equipment from manufacturers such as Distek, Erweka, Agilent or similar dissolution equipment provider?! OR are you a Chemist, Scientist or QC Analyst, Team Leader with extensive experience (3+ years) of using and troubleshooting the above types of Dissolution/Tablet Testing equipment in a GMP environment who is motivated to progress into an exciting Dissolution Field Service Engineer role?! If you said yes to the above, then this brand-new role could be perfect for you! The requirements of the Field Service Engineer - Pharmaceutical Dissolution: You will ideally already be an experienced Field Service Engineer with 2+ years of experience installing, validating, and servicing pharmaceutical dissolution/tablet testing equipment from manufacturers such as Distek, Erweka, Agilent or similar dissolution equipment You could also be a Chemist, Scientist or QC Analyst/Team Leader with extensive experience (3+ years) of using and troubleshooting the above types of Dissolution/Tablet Testing equipment in a GMP environment who is motivated to progress into a Dissolution Field Service Engineer role Experience working in a GMP environment is a must You will be educated in either a life science/chemistry or engineering subject Must hold a full UK driving license & valid passport with the ability to travel both in the UK to the Nordic region each month Experience of effective verbal communication skills in a customer facing or customer service environment, with excellent telephone manner The responsibilities of the Field Service Engineer - Pharmaceutical Dissolution: Travel to customer sites both in your UK region and the Nordics (Sweden, Finland, Norway & Denmark) when required to deliver routine planned maintenance and breakdown support for my clients market leading Pharmaceutical dissolution & tablet testing equipment Refurbish and validate equipment for the refurbished instrument program in line with SOPs at my clients UK facility Ientify new customers or new market segments that could become long term accounts Build and maintain relationships with existing and potential customers to allow continuation of business and win incremental business Perform onsite duties including, service, validation, repair, accurately and in a timely fashion Complete and submit all paperwork to the admin team Build and maintains relationship with existing and new customers Promote the company's brand and range of services where applicable Manage and be accountable for stock allocated to the service call Provide remote support via phone and email to customers where requested Maintain knowledge of the products and services Benefits: Negotiable & Highly Competitive Base Salary DOE Fully expensed company car (hire car provided during probation) Tax free daily allowance (£10 when in the field for up to 8 hours) Over time will be paid in following fiscal year (January) or this can be taken of during the year as recover days, so no impact is made on statutory holidays Pension - 6% employer contribution with a minimum 3% employee contribution after 3 months continuous employment 23 days holiday rising to 25 with continual service + 8 bank holidays Life Insurance (3x value of annual base salary) after 3 months continuous employment Laptop & Phone To be considered for this role you must have full right to work in the UK and hold a valid UK driving licence. If you require Visa sponsorship and/or don't have a valid UK licence, please don't apply.
Mar 16, 2024
Full time
Territory: Midland's region with national travel as required and travel to clients in the Nordic region (Norway, Sweden, Denmark, Finland areas) circa 1 week every two months Your Location: Living anywhere on territory in the Midlands i.e., Birmingham, Coventry, Leicester, Derby, Nottingham, Lincoln, Northampton areas Do you want to work for a global leader in the development and manufacture of cutting-edge semi & fully automated pharmaceutical dissolution tablet testing technology?! Are you already a Field Service Engineer with 2+ years of experience installing, validating, and servicing pharmaceutical dissolution/tablet testing equipment from manufacturers such as Distek, Erweka, Agilent or similar dissolution equipment provider?! OR are you a Chemist, Scientist or QC Analyst, Team Leader with extensive experience (3+ years) of using and troubleshooting the above types of Dissolution/Tablet Testing equipment in a GMP environment who is motivated to progress into an exciting Dissolution Field Service Engineer role?! If you said yes to the above, then this brand-new role could be perfect for you! The requirements of the Field Service Engineer - Pharmaceutical Dissolution: You will ideally already be an experienced Field Service Engineer with 2+ years of experience installing, validating, and servicing pharmaceutical dissolution/tablet testing equipment from manufacturers such as Distek, Erweka, Agilent or similar dissolution equipment You could also be a Chemist, Scientist or QC Analyst/Team Leader with extensive experience (3+ years) of using and troubleshooting the above types of Dissolution/Tablet Testing equipment in a GMP environment who is motivated to progress into a Dissolution Field Service Engineer role Experience working in a GMP environment is a must You will be educated in either a life science/chemistry or engineering subject Must hold a full UK driving license & valid passport with the ability to travel both in the UK to the Nordic region each month Experience of effective verbal communication skills in a customer facing or customer service environment, with excellent telephone manner The responsibilities of the Field Service Engineer - Pharmaceutical Dissolution: Travel to customer sites both in your UK region and the Nordics (Sweden, Finland, Norway & Denmark) when required to deliver routine planned maintenance and breakdown support for my clients market leading Pharmaceutical dissolution & tablet testing equipment Refurbish and validate equipment for the refurbished instrument program in line with SOPs at my clients UK facility Ientify new customers or new market segments that could become long term accounts Build and maintain relationships with existing and potential customers to allow continuation of business and win incremental business Perform onsite duties including, service, validation, repair, accurately and in a timely fashion Complete and submit all paperwork to the admin team Build and maintains relationship with existing and new customers Promote the company's brand and range of services where applicable Manage and be accountable for stock allocated to the service call Provide remote support via phone and email to customers where requested Maintain knowledge of the products and services Benefits: Negotiable & Highly Competitive Base Salary DOE Fully expensed company car (hire car provided during probation) Tax free daily allowance (£10 when in the field for up to 8 hours) Over time will be paid in following fiscal year (January) or this can be taken of during the year as recover days, so no impact is made on statutory holidays Pension - 6% employer contribution with a minimum 3% employee contribution after 3 months continuous employment 23 days holiday rising to 25 with continual service + 8 bank holidays Life Insurance (3x value of annual base salary) after 3 months continuous employment Laptop & Phone To be considered for this role you must have full right to work in the UK and hold a valid UK driving licence. If you require Visa sponsorship and/or don't have a valid UK licence, please don't apply.
Highgrove Recruitment Group Limited
Stafford, Staffordshire
Surveyor: Conduct Management/Refurbishment/Demolition asbestos surveys with meticulous attention to detail. On-the-Go: Explore multiple sites daily to ensure every survey meets our exacting standards. Care and Precision: Safeguard domestic and commercial properties with utmost care and precision. Sampling Mastery: Collect samples and make things right when necessary. Quality Control: Keep our reports top-notch, consistently meeting our KPIs. Digital Prowess: Input survey data with ease using our cutting-edge system (TEAMS). Professional Poise: Maintain professionalism in all interactions with clients, contractors, and residents. Compliance Champion: Uphold UKAS requirements every step of the way. Analyst: Air Quality Expertise: Execute various Air Fibre Monitoring tasks, including Personals, Backgrounds, Reassurance, and 4 Stage Clearances. On-the-Road Pro: Travel to multiple sites, equipped with a company vehicle. Survey Savvy: Conduct Management/Refurbishment/Demolition asbestos surveys with precision. Sample Specialist: Master the art of sample collection and remediation when needed. Digital Proficiency: Input survey data electronically using our advanced system (TEAMS). Client Liaison: Maintain professionalism while interacting with clients, contractors, and residents. Compliance Commitment: Uphold UKAS requirements as second nature, with comprehensive training provided. Slide Reader: Perform regular QC/RICE slide readings with accuracy. Requirements UK Driving Licence (required). The ability to work overtime when required. BOHS P402, P403, P404 certificates or equivalent. Extensive travel required, therefore flexibility in working hours is required
Mar 14, 2024
Full time
Surveyor: Conduct Management/Refurbishment/Demolition asbestos surveys with meticulous attention to detail. On-the-Go: Explore multiple sites daily to ensure every survey meets our exacting standards. Care and Precision: Safeguard domestic and commercial properties with utmost care and precision. Sampling Mastery: Collect samples and make things right when necessary. Quality Control: Keep our reports top-notch, consistently meeting our KPIs. Digital Prowess: Input survey data with ease using our cutting-edge system (TEAMS). Professional Poise: Maintain professionalism in all interactions with clients, contractors, and residents. Compliance Champion: Uphold UKAS requirements every step of the way. Analyst: Air Quality Expertise: Execute various Air Fibre Monitoring tasks, including Personals, Backgrounds, Reassurance, and 4 Stage Clearances. On-the-Road Pro: Travel to multiple sites, equipped with a company vehicle. Survey Savvy: Conduct Management/Refurbishment/Demolition asbestos surveys with precision. Sample Specialist: Master the art of sample collection and remediation when needed. Digital Proficiency: Input survey data electronically using our advanced system (TEAMS). Client Liaison: Maintain professionalism while interacting with clients, contractors, and residents. Compliance Commitment: Uphold UKAS requirements as second nature, with comprehensive training provided. Slide Reader: Perform regular QC/RICE slide readings with accuracy. Requirements UK Driving Licence (required). The ability to work overtime when required. BOHS P402, P403, P404 certificates or equivalent. Extensive travel required, therefore flexibility in working hours is required
Surveyor: Conduct Management/Refurbishment/Demolition asbestos surveys with meticulous attention to detail. On-the-Go: Explore multiple sites daily to ensure every survey meets our exacting standards. Care and Precision: Safeguard domestic and commercial properties with utmost care and precision. Sampling Mastery: Collect samples and make things right when necessary. Quality Control: Keep our reports top-notch, consistently meeting our KPIs. Digital Prowess: Input survey data with ease using our cutting-edge system (TEAMS). Professional Poise: Maintain professionalism in all interactions with clients, contractors, and residents. Compliance Champion: Uphold UKAS requirements every step of the way. Analyst: Air Quality Expertise: Execute various Air Fibre Monitoring tasks, including Personals, Backgrounds, Reassurance, and 4 Stage Clearances. On-the-Road Pro: Travel to multiple sites, equipped with a company vehicle. Survey Savvy: Conduct Management/Refurbishment/Demolition asbestos surveys with precision. Sample Specialist: Master the art of sample collection and remediation when needed. Digital Proficiency: Input survey data electronically using our advanced system (TEAMS). Client Liaison: Maintain professionalism while interacting with clients, contractors, and residents. Compliance Commitment: Uphold UKAS requirements as second nature, with comprehensive training provided. Slide Reader: Perform regular QC/RICE slide readings with accuracy. Requirements UK Driving Licence (required). The ability to work overtime when required. BOHS P402, P403, P404 certificates or equivalent. Extensive travel required, therefore flexibility in working hours is required
Mar 14, 2024
Full time
Surveyor: Conduct Management/Refurbishment/Demolition asbestos surveys with meticulous attention to detail. On-the-Go: Explore multiple sites daily to ensure every survey meets our exacting standards. Care and Precision: Safeguard domestic and commercial properties with utmost care and precision. Sampling Mastery: Collect samples and make things right when necessary. Quality Control: Keep our reports top-notch, consistently meeting our KPIs. Digital Prowess: Input survey data with ease using our cutting-edge system (TEAMS). Professional Poise: Maintain professionalism in all interactions with clients, contractors, and residents. Compliance Champion: Uphold UKAS requirements every step of the way. Analyst: Air Quality Expertise: Execute various Air Fibre Monitoring tasks, including Personals, Backgrounds, Reassurance, and 4 Stage Clearances. On-the-Road Pro: Travel to multiple sites, equipped with a company vehicle. Survey Savvy: Conduct Management/Refurbishment/Demolition asbestos surveys with precision. Sample Specialist: Master the art of sample collection and remediation when needed. Digital Proficiency: Input survey data electronically using our advanced system (TEAMS). Client Liaison: Maintain professionalism while interacting with clients, contractors, and residents. Compliance Commitment: Uphold UKAS requirements as second nature, with comprehensive training provided. Slide Reader: Perform regular QC/RICE slide readings with accuracy. Requirements UK Driving Licence (required). The ability to work overtime when required. BOHS P402, P403, P404 certificates or equivalent. Extensive travel required, therefore flexibility in working hours is required
Adecco Newbury are seeking a QC Data Reviewer to join a client based in Swindon. The main requirement is responsible for the GMP review of QC Chemistry analytical documentation and logbooks. This is an ongoing temporary position working Monday to Friday 8.30am to 4.30pm. Responsibilities: To perform GMP data review quality control analytical testing of incoming goods, intermediates and/or finished products under cGMP conditions for QC release or as part of stability studies. To provide support and training for QC Analysts to ensure that there is understanding of why any corrections are required and how to better present data in future. To author and review technical documentation including but not limited to standard operating procedures, investigations and reports. To perform tracking and trending of right first time (RFT) data for QC Chemistry with regards to analytical RFT and documentation RFT. To perform tracking and trending of Laboratory Investigations and Laboratory Events. To review QC logbooks for accuracy and completeness. To maintain own training records and support and train other team members as required. To participate in continuous improvement activities and look for further opportunities to progress the team/department. To communicate effectively with others on site and internationally, and to participate with them in problem solving activities. Ensure cGMP is applied in their area of work and comply with cGMP in all areas of the business. To work with HSE, cGMP and 5S in mind at all times. To carry out any other tasks which may be required from time to time. EH &S Understand emergency procedures and comply with safe systems of work. Ensure compliance with environment, health and safety rules, signage and instructions at all times. Ensure prompt reporting and investigation of all accidents, near misses and breaches of rules. Minimum Requirements/Qualifications: Degree in Chemistry or strongly related scientific discipline or equivalent Experience of instrumental and traditional analytical techniques. Ability to work to critical timelines Effective communication skills at all internal and external levels. Excellent attention to detail. Excellent organisational skills. Do you have experience in a similar role and all the relevant skills? If so, apply today Adecco Newbury. Please note: This position is based in Swindon, please only apply if you are willing and able to work in this location. All applications will be reviewed within five working days by one of our experienced consultants and successful applicants only will be contacted within that time frame. Please be assured that your details remain confidential, and they will not be sent out to our client(s) until you have been contacted by us and have given us your consent, in accordance with REC guidelines. Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.
Feb 01, 2024
Full time
Adecco Newbury are seeking a QC Data Reviewer to join a client based in Swindon. The main requirement is responsible for the GMP review of QC Chemistry analytical documentation and logbooks. This is an ongoing temporary position working Monday to Friday 8.30am to 4.30pm. Responsibilities: To perform GMP data review quality control analytical testing of incoming goods, intermediates and/or finished products under cGMP conditions for QC release or as part of stability studies. To provide support and training for QC Analysts to ensure that there is understanding of why any corrections are required and how to better present data in future. To author and review technical documentation including but not limited to standard operating procedures, investigations and reports. To perform tracking and trending of right first time (RFT) data for QC Chemistry with regards to analytical RFT and documentation RFT. To perform tracking and trending of Laboratory Investigations and Laboratory Events. To review QC logbooks for accuracy and completeness. To maintain own training records and support and train other team members as required. To participate in continuous improvement activities and look for further opportunities to progress the team/department. To communicate effectively with others on site and internationally, and to participate with them in problem solving activities. Ensure cGMP is applied in their area of work and comply with cGMP in all areas of the business. To work with HSE, cGMP and 5S in mind at all times. To carry out any other tasks which may be required from time to time. EH &S Understand emergency procedures and comply with safe systems of work. Ensure compliance with environment, health and safety rules, signage and instructions at all times. Ensure prompt reporting and investigation of all accidents, near misses and breaches of rules. Minimum Requirements/Qualifications: Degree in Chemistry or strongly related scientific discipline or equivalent Experience of instrumental and traditional analytical techniques. Ability to work to critical timelines Effective communication skills at all internal and external levels. Excellent attention to detail. Excellent organisational skills. Do you have experience in a similar role and all the relevant skills? If so, apply today Adecco Newbury. Please note: This position is based in Swindon, please only apply if you are willing and able to work in this location. All applications will be reviewed within five working days by one of our experienced consultants and successful applicants only will be contacted within that time frame. Please be assured that your details remain confidential, and they will not be sent out to our client(s) until you have been contacted by us and have given us your consent, in accordance with REC guidelines. Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.
Technical Leader - Analytical Development Partnering with a market leader in the CDMO space, with sites globally and with significant investment across their UK operations, I am supporting them continue their international expansion of services. Given this investment, there has been a sizeable increase of their analytical services offering for clients, meaning greater resource required across the analytical laboratories at all levels. This specific hire is for a Technical Leader in the development team. With a key focus on client management and team management, this person will have solid experience in analytical chemistry method development and validation - allowing them to troubleshoot and provide expert advice and guidance to clients on project milestones. Whilst you won't need to be hands on frequently, it will be necessary to step in as required and deal with out of specification issues in particular. A willingness to pass on your experience and commercial understanding is crucial. Given the way the business is expanding, development opportunities are genuine and discussed transparently from the start. Key experience: Chemistry based or Pharmaceutical Science degree (or equivalent) Experienced analytical development professional with at least 7 years experience across a range of analytical and wet chemistry methods GMP experience essential Management/supervisory experience essential Experience in overseeing OOS and compliance documentation Method validation experience essential A strong appreciation for a project focus in a client led environment is required - if you have worked in a CMO/CDMO/CRO setting, this would be advantageous QC, quality, control, analytical, testing, solid, dose, powders, liquids, raw, materials, stability, laboratory, analyst, technician, graduate, entry, GMP, manufacturing, HPLC, chromatography, GC, chemistry, development, validation, method, development, validation
Dec 06, 2023
Full time
Technical Leader - Analytical Development Partnering with a market leader in the CDMO space, with sites globally and with significant investment across their UK operations, I am supporting them continue their international expansion of services. Given this investment, there has been a sizeable increase of their analytical services offering for clients, meaning greater resource required across the analytical laboratories at all levels. This specific hire is for a Technical Leader in the development team. With a key focus on client management and team management, this person will have solid experience in analytical chemistry method development and validation - allowing them to troubleshoot and provide expert advice and guidance to clients on project milestones. Whilst you won't need to be hands on frequently, it will be necessary to step in as required and deal with out of specification issues in particular. A willingness to pass on your experience and commercial understanding is crucial. Given the way the business is expanding, development opportunities are genuine and discussed transparently from the start. Key experience: Chemistry based or Pharmaceutical Science degree (or equivalent) Experienced analytical development professional with at least 7 years experience across a range of analytical and wet chemistry methods GMP experience essential Management/supervisory experience essential Experience in overseeing OOS and compliance documentation Method validation experience essential A strong appreciation for a project focus in a client led environment is required - if you have worked in a CMO/CDMO/CRO setting, this would be advantageous QC, quality, control, analytical, testing, solid, dose, powders, liquids, raw, materials, stability, laboratory, analyst, technician, graduate, entry, GMP, manufacturing, HPLC, chromatography, GC, chemistry, development, validation, method, development, validation
REED Colchester are delighted to be recruiting for an amazing Governance and Quality Analyst role for a care company based in Central Colchester. Fixed Term 12 Months - Maternity Cover This job role is remote (working from home) however requires occasional travel to visit the office and clients (will vary but expected one or two days a week). Hours: Monday - Friday Standard Office Hours The Job Role: The Governance & Quality Analyst will work collaboratively across the company to support managers and their deputies to deliver a quality focused service which meets and exceeds the needs of our customers and regulators. The role will support managers in maintaining a standardised approach to CQC readiness and compliance through the use of Quality and Compliance systems. Key Outcomes • Support managers and deputies across the business to demonstrate the principles of good governance to meet regulatory requirements through the use of Quality and Compliance systems• Understand the new CQC Inspection Process, Regulations and Enforcement guidelines• Support the implementation and maintenance of the Compliance system to enable an effective and efficient method of recording, reviewing and reporting on governance and quality across the organisation• Support with the preparation, delivery and reporting of auditing across all Services• Support operational team to follow through the completion of action plans in a timely manner• Attend Governance meetings, taking minutes and providing data required where needed• Support with relevant contract monitoring requirements from Local Authorities, and where possible working with them to develop a standardised report which meets their requirements• Support Operations with CQC notifications regarding new services, change of provision or deregistration• Providing relevant information for the quarterly SQI report and any other related governance and quality reports• Preparation and communication of the On Call Rotas• Supporting managers with the Complaints, Compliments and Safeguarding recording processes and maintaining an oversight on the Compliance system• Managing any subject access requests from customers in tandem with the Data Protection Officer• Deputise for and support the Corporate Services Manager & Quality Analyst as required The Person: Good general standard of education (to GCSE level) including Mathematics & English or equivalent qualifications / experience. Strong Administration background required and computer literate. A car owner and full UK Clean Driving License required. Similar experience desirable Benefits HSF - Dental / Health cover (preferential contributory rates) Reward / Recognition programmes Empathy - our employee assistance programme When you need it - Sick leave, maternity & paternity Refer a Friend Scheme Pension and life assurance cover Disability Friendly If this role is what you are looking I urge to apply ASAP, as they are looking to start conducting interviews as soon as. I will be in touch if I agree you're are a good match. Best of luck
Dec 19, 2022
Full time
REED Colchester are delighted to be recruiting for an amazing Governance and Quality Analyst role for a care company based in Central Colchester. Fixed Term 12 Months - Maternity Cover This job role is remote (working from home) however requires occasional travel to visit the office and clients (will vary but expected one or two days a week). Hours: Monday - Friday Standard Office Hours The Job Role: The Governance & Quality Analyst will work collaboratively across the company to support managers and their deputies to deliver a quality focused service which meets and exceeds the needs of our customers and regulators. The role will support managers in maintaining a standardised approach to CQC readiness and compliance through the use of Quality and Compliance systems. Key Outcomes • Support managers and deputies across the business to demonstrate the principles of good governance to meet regulatory requirements through the use of Quality and Compliance systems• Understand the new CQC Inspection Process, Regulations and Enforcement guidelines• Support the implementation and maintenance of the Compliance system to enable an effective and efficient method of recording, reviewing and reporting on governance and quality across the organisation• Support with the preparation, delivery and reporting of auditing across all Services• Support operational team to follow through the completion of action plans in a timely manner• Attend Governance meetings, taking minutes and providing data required where needed• Support with relevant contract monitoring requirements from Local Authorities, and where possible working with them to develop a standardised report which meets their requirements• Support Operations with CQC notifications regarding new services, change of provision or deregistration• Providing relevant information for the quarterly SQI report and any other related governance and quality reports• Preparation and communication of the On Call Rotas• Supporting managers with the Complaints, Compliments and Safeguarding recording processes and maintaining an oversight on the Compliance system• Managing any subject access requests from customers in tandem with the Data Protection Officer• Deputise for and support the Corporate Services Manager & Quality Analyst as required The Person: Good general standard of education (to GCSE level) including Mathematics & English or equivalent qualifications / experience. Strong Administration background required and computer literate. A car owner and full UK Clean Driving License required. Similar experience desirable Benefits HSF - Dental / Health cover (preferential contributory rates) Reward / Recognition programmes Empathy - our employee assistance programme When you need it - Sick leave, maternity & paternity Refer a Friend Scheme Pension and life assurance cover Disability Friendly If this role is what you are looking I urge to apply ASAP, as they are looking to start conducting interviews as soon as. I will be in touch if I agree you're are a good match. Best of luck
Contract Type: Permanent Salary: Earnings circa £31,600/yr Job Elements This is a shift based role working 38hrs per week, mornings (6am-2pm) and afternoons (2-10) on a weekly rotation Perform the analysis of starting materials, intermediates and finished products in accordance with written procedures click apply for full job details
Dec 15, 2022
Full time
Contract Type: Permanent Salary: Earnings circa £31,600/yr Job Elements This is a shift based role working 38hrs per week, mornings (6am-2pm) and afternoons (2-10) on a weekly rotation Perform the analysis of starting materials, intermediates and finished products in accordance with written procedures click apply for full job details
Just Life Sciences are working with a leading Pharma business who have experienced exceptional growth of the business in the last two years and who are now looking to strengthen their Analytical Services department. We are looking for experienced Analysts for Development and Operations, and these will be on 2 shift patterns alternating form 6am to 2pm and 12pm to 8pm Mon to Fri. Should you be successful Your responsibilities will be Use, familiarity and expertise in a range of analytical techniques, instrumentation and software, such as GC, HPLC, FTIR, ICP, Auto-titration and Karl Fischer to test both finished products and raw materials Troubleshooting and problem solving for routine methods and afore mentioned equipment Developing and validating test methods and equipment Preparing specifications, standard test methods, operating procedures and performing risk assessments Analysis on varying Drug compounds yet with specific understanding of the Largest Pharmacopoeia being USP, EP, JP and BP. As such you will have ideally worked with HPLC, Dissolution Chambers, and have worked with Content of Active Ingredient, Uniformity of Content, Uniformity of Weight, Disintegration Time Test and Dissolution Test. Qualifications/Experience Degree (or equivalent) in Chemistry or related science subject with a significant Analytical component. Minimum of 1 years QC Analysis using HPLC Experience with High Performance Liquid Chromatography (mandatory). Experience in a GMP compliant environment (preferred). Detail orientated person and highly organised. Proactive personable to ensure consistent levels of lab organisation are achieved. Interested please contact justyn at justlifesciences dot com
Dec 10, 2022
Full time
Just Life Sciences are working with a leading Pharma business who have experienced exceptional growth of the business in the last two years and who are now looking to strengthen their Analytical Services department. We are looking for experienced Analysts for Development and Operations, and these will be on 2 shift patterns alternating form 6am to 2pm and 12pm to 8pm Mon to Fri. Should you be successful Your responsibilities will be Use, familiarity and expertise in a range of analytical techniques, instrumentation and software, such as GC, HPLC, FTIR, ICP, Auto-titration and Karl Fischer to test both finished products and raw materials Troubleshooting and problem solving for routine methods and afore mentioned equipment Developing and validating test methods and equipment Preparing specifications, standard test methods, operating procedures and performing risk assessments Analysis on varying Drug compounds yet with specific understanding of the Largest Pharmacopoeia being USP, EP, JP and BP. As such you will have ideally worked with HPLC, Dissolution Chambers, and have worked with Content of Active Ingredient, Uniformity of Content, Uniformity of Weight, Disintegration Time Test and Dissolution Test. Qualifications/Experience Degree (or equivalent) in Chemistry or related science subject with a significant Analytical component. Minimum of 1 years QC Analysis using HPLC Experience with High Performance Liquid Chromatography (mandatory). Experience in a GMP compliant environment (preferred). Detail orientated person and highly organised. Proactive personable to ensure consistent levels of lab organisation are achieved. Interested please contact justyn at justlifesciences dot com
QCL Analyst Temporary Liverpool £12.50ph Kelly Services, working with a global Pharmaceutical business, undergoing a period of steady growth are now looking to add a number of QCL Analysts to join the team on a temporary ongoing basis to assist in additional workloads. We are keen to speak with individuals with a background of analysis in either HPLC, Micro or Wet chemistry. You will be responsible for safely performing laboratory analyses of purchased and manufactured materials, utilities/EM and stability samples to cGMP and Regulatory requirements. Functions, Duties, Tasks: Maintain laboratory and office areas in compliance with EHS and cGMP requirements. Archive completed laboratory documentation in a timely manner. Chemical and/or microbial based analyses of purchased and manufactured materials, utilities/EM, stability samples and non-routine samples. Report and approve results using standard laboratory systems ensuring all statistical monitoring charts (paper and electronic) are updated in a timely manner. Perform all aspects of sample handling, e.g. sample receipt, storage and disposal as per procedures. If authorised, perform second person verification of analytical data generated in QCL as per procedures. Liaise with Supervision and planners to prioritise workload to ensure OSSCE lead times and expected customer service levels are met. Conduct the equipment calibrations, maintenance and IQ/OQ that you are trained to perform. Train other QCL staff in these tasks as appropriate. Write, update and review analytical workbooks, methods and procedures. Perform analyses and document results to support method verifications, validations and transfers. Assist the QCL Scientist/Equipment group when required, by participating in analytical investigations, investigative testing and method/equipment fault finding and troubleshooting. Follow lab purchasing procedures to ensure laboratory remains sufficiently stocked with standards/reagents and consumables. If trained and authorised to do so, purchase standards/reagents/consumables. Communicate with regulatory auditors such as GQA, MHRA, FDA etc in accordance with company policy. If you are interested in this position or for more information, please apply or contact Kelly Scientific on Kelly Services are acting as an Employment Business in relation to this role. Should you choose to apply, your information will be processed in accordance with Kelly's Privacy Statement. For information regarding data protection at Kelly, please visit the Kelly website and have a look into the Privacy Statement. As an Equal Opportunities employer we welcome applications from all suitably qualified persons regardless of their race, sex, disability, religion/belief, sexual orientation or age.
Dec 10, 2022
Full time
QCL Analyst Temporary Liverpool £12.50ph Kelly Services, working with a global Pharmaceutical business, undergoing a period of steady growth are now looking to add a number of QCL Analysts to join the team on a temporary ongoing basis to assist in additional workloads. We are keen to speak with individuals with a background of analysis in either HPLC, Micro or Wet chemistry. You will be responsible for safely performing laboratory analyses of purchased and manufactured materials, utilities/EM and stability samples to cGMP and Regulatory requirements. Functions, Duties, Tasks: Maintain laboratory and office areas in compliance with EHS and cGMP requirements. Archive completed laboratory documentation in a timely manner. Chemical and/or microbial based analyses of purchased and manufactured materials, utilities/EM, stability samples and non-routine samples. Report and approve results using standard laboratory systems ensuring all statistical monitoring charts (paper and electronic) are updated in a timely manner. Perform all aspects of sample handling, e.g. sample receipt, storage and disposal as per procedures. If authorised, perform second person verification of analytical data generated in QCL as per procedures. Liaise with Supervision and planners to prioritise workload to ensure OSSCE lead times and expected customer service levels are met. Conduct the equipment calibrations, maintenance and IQ/OQ that you are trained to perform. Train other QCL staff in these tasks as appropriate. Write, update and review analytical workbooks, methods and procedures. Perform analyses and document results to support method verifications, validations and transfers. Assist the QCL Scientist/Equipment group when required, by participating in analytical investigations, investigative testing and method/equipment fault finding and troubleshooting. Follow lab purchasing procedures to ensure laboratory remains sufficiently stocked with standards/reagents and consumables. If trained and authorised to do so, purchase standards/reagents/consumables. Communicate with regulatory auditors such as GQA, MHRA, FDA etc in accordance with company policy. If you are interested in this position or for more information, please apply or contact Kelly Scientific on Kelly Services are acting as an Employment Business in relation to this role. Should you choose to apply, your information will be processed in accordance with Kelly's Privacy Statement. For information regarding data protection at Kelly, please visit the Kelly website and have a look into the Privacy Statement. As an Equal Opportunities employer we welcome applications from all suitably qualified persons regardless of their race, sex, disability, religion/belief, sexual orientation or age.
QC Shift Analyst - Food manufacturing Daventry Permanent Salary - £26,000 per annum Hours: 37.5 per week - A 2-shift rotating system operates; 06:00-14:00 and 12:00-20:00 Monday to Friday Do you have a real interest and passion in the analysis and properties of chemicals and organic molecules in particular? Our Daventry based client are looking to recruit a QC Analyst to join their quality depar click apply for full job details
Dec 08, 2022
Full time
QC Shift Analyst - Food manufacturing Daventry Permanent Salary - £26,000 per annum Hours: 37.5 per week - A 2-shift rotating system operates; 06:00-14:00 and 12:00-20:00 Monday to Friday Do you have a real interest and passion in the analysis and properties of chemicals and organic molecules in particular? Our Daventry based client are looking to recruit a QC Analyst to join their quality depar click apply for full job details
We are currently looking for a Material QC Analyst to join a leading BioTech company based in the London area. As the Material QC Analyst you will be responsible for KEY DUTIES AND RESPONSIBILITIES: Your duties as the Material QC Analyst will be varied however the key duties and responsibilities are as follows: 1 click apply for full job details
Dec 08, 2022
Full time
We are currently looking for a Material QC Analyst to join a leading BioTech company based in the London area. As the Material QC Analyst you will be responsible for KEY DUTIES AND RESPONSIBILITIES: Your duties as the Material QC Analyst will be varied however the key duties and responsibilities are as follows: 1 click apply for full job details
CK Group are recruiting for a Quality Analyst to join a materials manufacturing company at their site based in Runcorn on a full time, permanent basis. The Company: Our client is a leading manufacturer of niche materials used in a range of commercial applications. They are also committed to R&D. Recent investments obtained by the company allowed them to build and commission a significant new production facility at their Runcorn site which doubles the production area and provides the potential to generate revenue three to four times higher than the original plant.Our client places a lot of importance on health and wellbeing, and allowing everyone to be able to balance the needs of work and home, which is reflected in the benefits they offer. Salary: £20,000 - £23,000 per annum (depending on experience, with scope to go a little higher for more experienced candidate) Other benefits include: Bonus scheme, Company share option scheme, 25 days holiday per year plus Bank Holidays, opportunity for sponsorship with professional qualifications, Company events, Life insurance scheme (4 x salary), Company pension (7.5% contribution), Wellbeing Policies, free onsite parking, Cycle-to-work scheme Location: The Quality Analyst will be based at the company's site in Runcorn, easily commutable from Warrington, Widnes, Frodsham, Chester, Liverpool and Manchester. There is also flexibility to work at other locations as the business may reasonably require. Hours of work: Full-time, 35 hours per week, Monday - Friday. Role: This is a hands-on role involving analysis of materials and maintenance and calibration of equipment. It requires flexibility to work with a wide and developing range of measurement and analytical techniques and includes Health and Safety responsibilities, participation in continuous improvement programmes and laboratory housekeeping. Key Responsibilities: Carry out routine and non-routine QC testing of nanomaterials samples, precursors and incoming raw materials using a range of analytical techniques including (but not limited to) GC-FID, TGA, FT-IR, Karl Fischer titrations, UV-Vis-NIR and fluorescence spectroscopy Develop personal expertise in the range of analytical techniques used by the company Ensure that all analytical instruments are maintained in working order, calibrated and serviced Report and investigate quality failures Ensure compliance with ISO 9001 quality standards when analysing samples and recording data Critically evaluate QC procedures and assist in the development and improvement of analytical methods by working closely with R&D and Production teams Prepare COSHH forms and Risk Assessments Carry Safety and Quality audits as required Your Background: BSc. (or equivalent) in Chemistry or similar subject with a significant chemistry portion. Experience in one or more of the analytical techniques listed above (experience working within an ISO-certified laboratory is advantageous). Ability to work effectively in a small team and across multiple projects simultaneously Ability to plan ahead, prioritise and address forthcoming issues Flexibility to work under strict deadlines and changing priorities Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 54807 in all correspondence.
Dec 05, 2022
Full time
CK Group are recruiting for a Quality Analyst to join a materials manufacturing company at their site based in Runcorn on a full time, permanent basis. The Company: Our client is a leading manufacturer of niche materials used in a range of commercial applications. They are also committed to R&D. Recent investments obtained by the company allowed them to build and commission a significant new production facility at their Runcorn site which doubles the production area and provides the potential to generate revenue three to four times higher than the original plant.Our client places a lot of importance on health and wellbeing, and allowing everyone to be able to balance the needs of work and home, which is reflected in the benefits they offer. Salary: £20,000 - £23,000 per annum (depending on experience, with scope to go a little higher for more experienced candidate) Other benefits include: Bonus scheme, Company share option scheme, 25 days holiday per year plus Bank Holidays, opportunity for sponsorship with professional qualifications, Company events, Life insurance scheme (4 x salary), Company pension (7.5% contribution), Wellbeing Policies, free onsite parking, Cycle-to-work scheme Location: The Quality Analyst will be based at the company's site in Runcorn, easily commutable from Warrington, Widnes, Frodsham, Chester, Liverpool and Manchester. There is also flexibility to work at other locations as the business may reasonably require. Hours of work: Full-time, 35 hours per week, Monday - Friday. Role: This is a hands-on role involving analysis of materials and maintenance and calibration of equipment. It requires flexibility to work with a wide and developing range of measurement and analytical techniques and includes Health and Safety responsibilities, participation in continuous improvement programmes and laboratory housekeeping. Key Responsibilities: Carry out routine and non-routine QC testing of nanomaterials samples, precursors and incoming raw materials using a range of analytical techniques including (but not limited to) GC-FID, TGA, FT-IR, Karl Fischer titrations, UV-Vis-NIR and fluorescence spectroscopy Develop personal expertise in the range of analytical techniques used by the company Ensure that all analytical instruments are maintained in working order, calibrated and serviced Report and investigate quality failures Ensure compliance with ISO 9001 quality standards when analysing samples and recording data Critically evaluate QC procedures and assist in the development and improvement of analytical methods by working closely with R&D and Production teams Prepare COSHH forms and Risk Assessments Carry Safety and Quality audits as required Your Background: BSc. (or equivalent) in Chemistry or similar subject with a significant chemistry portion. Experience in one or more of the analytical techniques listed above (experience working within an ISO-certified laboratory is advantageous). Ability to work effectively in a small team and across multiple projects simultaneously Ability to plan ahead, prioritise and address forthcoming issues Flexibility to work under strict deadlines and changing priorities Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 54807 in all correspondence.
We are currently looking for an Analytical Chemist for growing pharmaceutical company in the South East. As an Analytical Chemist you will carry out laboratory analysis using a range of techniques including HPLC, UPLC, GC and FTIR in support of R&D projects. Responsibilities include: Analyse a range of samples using analytical instrumentation such as HPLC, GC, UV and FTIR Run/ support stability studies. Carry out method validation, troubleshooting and tech transfers. Ensure all work is carried out to cGMP standards Ideal candidates will be Degree, masters (BSc, MSc, MChem) qualified in chemistry, analytical chemistry or forensic sciences and have some previous experience working as an Analytical Chemist or QC Analyst in industry using HPLC. This is a rapidly growing company that offers a highly competitive salary and benefits package. Analytical Chemist roles available include normal days (Monday-Friday) and on shifts (The shift allowance is very attractive!) To apply to the Analytical Chemist roles please send your CV to Peter at Rowland Talent Solutions. Key words: QC, Quality Control, Analyst, Chemistry, Laboratory, GMP, Pharmaceutical, HPLC
Dec 02, 2022
Full time
We are currently looking for an Analytical Chemist for growing pharmaceutical company in the South East. As an Analytical Chemist you will carry out laboratory analysis using a range of techniques including HPLC, UPLC, GC and FTIR in support of R&D projects. Responsibilities include: Analyse a range of samples using analytical instrumentation such as HPLC, GC, UV and FTIR Run/ support stability studies. Carry out method validation, troubleshooting and tech transfers. Ensure all work is carried out to cGMP standards Ideal candidates will be Degree, masters (BSc, MSc, MChem) qualified in chemistry, analytical chemistry or forensic sciences and have some previous experience working as an Analytical Chemist or QC Analyst in industry using HPLC. This is a rapidly growing company that offers a highly competitive salary and benefits package. Analytical Chemist roles available include normal days (Monday-Friday) and on shifts (The shift allowance is very attractive!) To apply to the Analytical Chemist roles please send your CV to Peter at Rowland Talent Solutions. Key words: QC, Quality Control, Analyst, Chemistry, Laboratory, GMP, Pharmaceutical, HPLC
Salary 80,000 - 85,000 GBP per year Requirements: - Senior Business Analyst with Understanding of investments, lending, and equity. Must be able to Write a clear business requirement document (BRD).in the form of user stories in Jira Ability to raise a defect, and experience in Agile methodologies Waterfall model Interaction with all stakeholders, analysis, and requirement documentation, creating test case scenario, Acceptance Criteria, documentation in QC, test execution and test result documentation. Must acquire business knowledge, understand business analyst process, and perform testing of the new requirement in the system Responsibilities: - Performs and coordinates the analysis and design of business systems. Develops and maintains a thorough understanding of the needs of the assigned customer group from the business and technical perspective. Works closely with clients and with other system groups to capture business requirements and see them through implementation. Develops and executes systems testing. Acts as a liaison between the business user groups and the technical systems groups. This resource type provides analytical, technical, business and management expertise to the group and completes assignments which require this expertise. The resource may be required to lead teams of up to 10 professionals or operations personnel. This resource will respond and resolve issues beyond standard management requests as well as using independent judgment to make decisions where no clear precedents exist and should typically be used for a senior or lead level resource Technologies: - JIRA More: Strong analytical skills Ability to collaborate Adaptability Excellent communication skills Innovation, Inquisitive mind, endless curiosity, and passion for learning about customers, industries, and new approaches to doing things, how end users perform their jobs, industry challenges and solutions. Strong self-starter with the ability to effectively build, develop and manage relationships with internal and client stakeholders.
Nov 24, 2022
Full time
Salary 80,000 - 85,000 GBP per year Requirements: - Senior Business Analyst with Understanding of investments, lending, and equity. Must be able to Write a clear business requirement document (BRD).in the form of user stories in Jira Ability to raise a defect, and experience in Agile methodologies Waterfall model Interaction with all stakeholders, analysis, and requirement documentation, creating test case scenario, Acceptance Criteria, documentation in QC, test execution and test result documentation. Must acquire business knowledge, understand business analyst process, and perform testing of the new requirement in the system Responsibilities: - Performs and coordinates the analysis and design of business systems. Develops and maintains a thorough understanding of the needs of the assigned customer group from the business and technical perspective. Works closely with clients and with other system groups to capture business requirements and see them through implementation. Develops and executes systems testing. Acts as a liaison between the business user groups and the technical systems groups. This resource type provides analytical, technical, business and management expertise to the group and completes assignments which require this expertise. The resource may be required to lead teams of up to 10 professionals or operations personnel. This resource will respond and resolve issues beyond standard management requests as well as using independent judgment to make decisions where no clear precedents exist and should typically be used for a senior or lead level resource Technologies: - JIRA More: Strong analytical skills Ability to collaborate Adaptability Excellent communication skills Innovation, Inquisitive mind, endless curiosity, and passion for learning about customers, industries, and new approaches to doing things, how end users perform their jobs, industry challenges and solutions. Strong self-starter with the ability to effectively build, develop and manage relationships with internal and client stakeholders.
QC Senior Sponsor Contracts Manager Summary: Manages Quality Control of all client deliverables within the Global Deal and Contract Management (GDCM) group. Guarantees high quality of departmental output through detailed review of both contract documentation and study budgets. Ensures all deliverables conform to both client expectations and audit requirements. Provides detailed and constructive feedback to internal stakeholders and works with them to refine contractual materials. Tracks adherence to company processes and provides regular performance feedback. Why Syneos Health • means we're committed to our Total Self culture - where everyone can authentically be themselves. Our Total Self culture is what unites us globally, and we know every person's unique contributions make a difference. • We believe our success is a direct result of the people who are driving it - you! We value your dedication to care for our customers and patients, so we want to focus on taking care of you. That's why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong. Job responsibilities : Analytically reviews the more complex budget tools and contractual materials from a Syneos Health, client and audit perspective to ensure the highest possible quality of output. Proactively works with contract analysts to refine deliverables in accordance with existing QC checklists and company policies. Evaluates all budget commentary to ensure a clear, concise and robust narrative. Assesses validity of study pricing and suitability of budgets prior to client delivery. Ensures consistency between pricing tools, budget grids, payment schedules and all contractual documentation. Utilizes QC checklists to perform a thorough review of Change Order, Change Notification Form and Ballpark documentation to ensure quality and consistency. Ensures all legal entities and defined terms are correct, appropriate and applied consistently throughout documents. Validates the presence and accuracy of inflation language if applicable. Maintains a high level of flexibility and adaptability. Proactively creates and revises priorities as the need arises whilst working toward standard cycle times of review. Supports the Change Order process through expeditious reviews and the provision of concise feedback. Identifies and raises issues before they become critical and adjusts quickly to the changes of a dynamic organization. Ensures adherence to Contract Management systems by reviewing records during the QC process. Reviews these systems to drive compliance with both GDCM and Syneos Health reporting processes and approval policies. Evaluates the performance of analysts within the GDCM group by assessing the quality of materials submitted for QC and providing performance feedback on a monthly basis. Assists with ownership of this performance report as needed. Updates and maintains departmental template and process documents. Leads QC training for the Client Contracting Solutions group as needed. Assists with audit inquiries as needed. Mentors members of the QC team as needed. Performs other duties as assigned. What we're looking for: BA/BS degree in a Business Administration or Finance with a minimum of 7 years' experience preferably in budgeting, finance, proposal development and/or contracts management within a clinical research/pharmaceutical environment; or equivalent combination of education, training and experience. Flexibility in responding to job demands. Have excellent problems solving skills and outstanding attention to detail. Ability to perform several tasks simultaneously to meet critical deadlines and possess strong analytical skills. Knowledge of Microsoft Excel, Word and understanding of costing models. Ability to review and interpret budgets. Ability to work successfully in a team environment and maintain effective working relationships with colleagues and manager. Demonstrates effective time management skills. Ability to prioritize multiple tasks with management guidance and oversight. Excellent interpersonal, verbal and written communication skills. Demonstrates a positive and flexible attitude toward new and/or unconventional work assignments. Ability to consistently perform and deliver a high quality work product. Excellent organizational skills. Ability to work well under pressure and adapt to changing priorities. Knowledge of clinical trial proposal process and budget management. Professional ability to interact with individuals at all levels and different personalities. Proficiency in mathematics, written language and ability to work with both budgets and text. Good interpersonal skills and ability to work well with others. Disclaimer: Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.
Sep 24, 2022
Full time
QC Senior Sponsor Contracts Manager Summary: Manages Quality Control of all client deliverables within the Global Deal and Contract Management (GDCM) group. Guarantees high quality of departmental output through detailed review of both contract documentation and study budgets. Ensures all deliverables conform to both client expectations and audit requirements. Provides detailed and constructive feedback to internal stakeholders and works with them to refine contractual materials. Tracks adherence to company processes and provides regular performance feedback. Why Syneos Health • means we're committed to our Total Self culture - where everyone can authentically be themselves. Our Total Self culture is what unites us globally, and we know every person's unique contributions make a difference. • We believe our success is a direct result of the people who are driving it - you! We value your dedication to care for our customers and patients, so we want to focus on taking care of you. That's why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong. Job responsibilities : Analytically reviews the more complex budget tools and contractual materials from a Syneos Health, client and audit perspective to ensure the highest possible quality of output. Proactively works with contract analysts to refine deliverables in accordance with existing QC checklists and company policies. Evaluates all budget commentary to ensure a clear, concise and robust narrative. Assesses validity of study pricing and suitability of budgets prior to client delivery. Ensures consistency between pricing tools, budget grids, payment schedules and all contractual documentation. Utilizes QC checklists to perform a thorough review of Change Order, Change Notification Form and Ballpark documentation to ensure quality and consistency. Ensures all legal entities and defined terms are correct, appropriate and applied consistently throughout documents. Validates the presence and accuracy of inflation language if applicable. Maintains a high level of flexibility and adaptability. Proactively creates and revises priorities as the need arises whilst working toward standard cycle times of review. Supports the Change Order process through expeditious reviews and the provision of concise feedback. Identifies and raises issues before they become critical and adjusts quickly to the changes of a dynamic organization. Ensures adherence to Contract Management systems by reviewing records during the QC process. Reviews these systems to drive compliance with both GDCM and Syneos Health reporting processes and approval policies. Evaluates the performance of analysts within the GDCM group by assessing the quality of materials submitted for QC and providing performance feedback on a monthly basis. Assists with ownership of this performance report as needed. Updates and maintains departmental template and process documents. Leads QC training for the Client Contracting Solutions group as needed. Assists with audit inquiries as needed. Mentors members of the QC team as needed. Performs other duties as assigned. What we're looking for: BA/BS degree in a Business Administration or Finance with a minimum of 7 years' experience preferably in budgeting, finance, proposal development and/or contracts management within a clinical research/pharmaceutical environment; or equivalent combination of education, training and experience. Flexibility in responding to job demands. Have excellent problems solving skills and outstanding attention to detail. Ability to perform several tasks simultaneously to meet critical deadlines and possess strong analytical skills. Knowledge of Microsoft Excel, Word and understanding of costing models. Ability to review and interpret budgets. Ability to work successfully in a team environment and maintain effective working relationships with colleagues and manager. Demonstrates effective time management skills. Ability to prioritize multiple tasks with management guidance and oversight. Excellent interpersonal, verbal and written communication skills. Demonstrates a positive and flexible attitude toward new and/or unconventional work assignments. Ability to consistently perform and deliver a high quality work product. Excellent organizational skills. Ability to work well under pressure and adapt to changing priorities. Knowledge of clinical trial proposal process and budget management. Professional ability to interact with individuals at all levels and different personalities. Proficiency in mathematics, written language and ability to work with both budgets and text. Good interpersonal skills and ability to work well with others. Disclaimer: Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.