Specialist Pharmacy or Science Manufacturing Technician - Aseptic Services / Administration (Band 5) Northampton General Hospital University Hospitals of Northamptonshire NHS Group Full-Time, Perm or Bank Start Date: ASAP About the Role We are working with Northampton General Hospital to recruit a Band 5 Specialist Pharmacy or Science Manufacturing Technician to join their Aseptic Services Unit (ASU). This is a key role within a highly specialised pharmacy service, supporting the preparation and supply of aseptically prepared intravenous medicines, including chemotherapy and parenteral nutrition. Key Responsibilities Support the preparation and dispensing of aseptic medicines (patient-specific and batch production) Undertake final checking and release of aseptically prepared products (once competent) Work within cleanroom and isolator environments, following Good Manufacturing Practice (GMP) Coordinate day-to-day workload within the Aseptic Unit to ensure timely delivery of treatments Support cost improvement initiatives, data analysis, and reporting of key performance metrics Manage charging processes for external customers and resolve invoice queries Contribute to quality systems, audits, and service improvement initiatives Support training and supervision of junior staff where required This role combines technical aseptic services work with administrative and analytical responsibilities, offering a varied and rewarding position. Essential Requirements Qualified Pharmacy Technician (NVQ Level 3 or equivalent), or Science Manufacturing Technician qualification, or relevant degree in pharmaceutical science or related field Professional registration with GPhC, Science Council or RPS Knowledge and experience of aseptic preparation and GMP Strong attention to detail and accuracy Good communication, organisation, and IT skills Desirable Experience in hospital aseptic services Experience in final checking and releasing products Experience with quality systems, audits, or CAPA processes Experience supervising or training staff Knowledge of electronic quality management systems (EQMS) Why Apply? Work within a specialist aseptic and cancer services environment Gain experience in licensed pharmaceutical manufacturing Opportunity to develop skills in quality systems, data analysis, and service improvement Be part of a supportive multidisciplinary pharmacy team Contribute directly to patient safety and treatment delivery
Aug 26, 2026
Full time
Specialist Pharmacy or Science Manufacturing Technician - Aseptic Services / Administration (Band 5) Northampton General Hospital University Hospitals of Northamptonshire NHS Group Full-Time, Perm or Bank Start Date: ASAP About the Role We are working with Northampton General Hospital to recruit a Band 5 Specialist Pharmacy or Science Manufacturing Technician to join their Aseptic Services Unit (ASU). This is a key role within a highly specialised pharmacy service, supporting the preparation and supply of aseptically prepared intravenous medicines, including chemotherapy and parenteral nutrition. Key Responsibilities Support the preparation and dispensing of aseptic medicines (patient-specific and batch production) Undertake final checking and release of aseptically prepared products (once competent) Work within cleanroom and isolator environments, following Good Manufacturing Practice (GMP) Coordinate day-to-day workload within the Aseptic Unit to ensure timely delivery of treatments Support cost improvement initiatives, data analysis, and reporting of key performance metrics Manage charging processes for external customers and resolve invoice queries Contribute to quality systems, audits, and service improvement initiatives Support training and supervision of junior staff where required This role combines technical aseptic services work with administrative and analytical responsibilities, offering a varied and rewarding position. Essential Requirements Qualified Pharmacy Technician (NVQ Level 3 or equivalent), or Science Manufacturing Technician qualification, or relevant degree in pharmaceutical science or related field Professional registration with GPhC, Science Council or RPS Knowledge and experience of aseptic preparation and GMP Strong attention to detail and accuracy Good communication, organisation, and IT skills Desirable Experience in hospital aseptic services Experience in final checking and releasing products Experience with quality systems, audits, or CAPA processes Experience supervising or training staff Knowledge of electronic quality management systems (EQMS) Why Apply? Work within a specialist aseptic and cancer services environment Gain experience in licensed pharmaceutical manufacturing Opportunity to develop skills in quality systems, data analysis, and service improvement Be part of a supportive multidisciplinary pharmacy team Contribute directly to patient safety and treatment delivery
CBSbutler Holdings Limited trading as CBSbutler
Towcester, Northamptonshire
Equipment Technician Location: Northamptonshire Salary: Up to 40,000 + 35% Shift Allowance + Excellent Benefits Shift Pattern: Continental - 2 Days / 2 Nights / 4 Off We are seeking an experienced Equipment Technician to join a highly advanced engineering and manufacturing facility, supporting the operation and maintenance of complex semiconductor production equipment. This is a hands-on role working with sophisticated electro-mechanical, vacuum, pneumatic, electrical and RF systems within a high-tech cleanroom environment. Key Responsibilities Diagnose, repair and maintain advanced manufacturing and process equipment. Provide rapid engineering response to minimise equipment downtime. Carry out planned and preventative maintenance to maximise equipment uptime and performance. Fault-find across electrical, electronic, mechanical, vacuum and pneumatic systems. Support equipment including lithography, etch, deposition and epitaxy systems. Work safely with specialist gases, chemicals and associated delivery and exhaust systems. Manage critical spare parts and support continuous improvement initiatives. Maintain accurate technical documentation, procedures and maintenance records. Work closely with Engineering, Manufacturing, Facilities and other technical teams. Skills & Experience Apprenticeship, HNC, HND or Degree in Electrical or Mechanical Engineering, or equivalent experience. Strong fault-finding and diagnostic skills across complex electro-mechanical systems. Experience within a high-tech, precision or safety-critical engineering environment. Ability to interpret technical drawings and documentation. Experience following detailed procedures, risk assessments and method statements. Strong communication, organisational and problem-solving skills. Candidates from semiconductor, aerospace, defence, automotive, pharmaceuticals, oil & gas, power generation or Armed Forces engineering backgrounds are encouraged to apply. Semiconductor or cleanroom experience is advantageous but not essential. Additional Information 40.3 hours per week. Continental shift pattern: 2 days, 2 nights, 4 days off . 12-hour shifts, including weekends and bank holidays. Cleanroom-based working environment. SCBA use required; training and relevant assessments provided. Forklift training can be provided. Due to the rural location, a full UK driving licence and access to your own transport are essential . This is an excellent opportunity to work with cutting-edge technology in a highly specialised engineering environment, with strong career development opportunities and an excellent benefits package.
Aug 20, 2026
Full time
Equipment Technician Location: Northamptonshire Salary: Up to 40,000 + 35% Shift Allowance + Excellent Benefits Shift Pattern: Continental - 2 Days / 2 Nights / 4 Off We are seeking an experienced Equipment Technician to join a highly advanced engineering and manufacturing facility, supporting the operation and maintenance of complex semiconductor production equipment. This is a hands-on role working with sophisticated electro-mechanical, vacuum, pneumatic, electrical and RF systems within a high-tech cleanroom environment. Key Responsibilities Diagnose, repair and maintain advanced manufacturing and process equipment. Provide rapid engineering response to minimise equipment downtime. Carry out planned and preventative maintenance to maximise equipment uptime and performance. Fault-find across electrical, electronic, mechanical, vacuum and pneumatic systems. Support equipment including lithography, etch, deposition and epitaxy systems. Work safely with specialist gases, chemicals and associated delivery and exhaust systems. Manage critical spare parts and support continuous improvement initiatives. Maintain accurate technical documentation, procedures and maintenance records. Work closely with Engineering, Manufacturing, Facilities and other technical teams. Skills & Experience Apprenticeship, HNC, HND or Degree in Electrical or Mechanical Engineering, or equivalent experience. Strong fault-finding and diagnostic skills across complex electro-mechanical systems. Experience within a high-tech, precision or safety-critical engineering environment. Ability to interpret technical drawings and documentation. Experience following detailed procedures, risk assessments and method statements. Strong communication, organisational and problem-solving skills. Candidates from semiconductor, aerospace, defence, automotive, pharmaceuticals, oil & gas, power generation or Armed Forces engineering backgrounds are encouraged to apply. Semiconductor or cleanroom experience is advantageous but not essential. Additional Information 40.3 hours per week. Continental shift pattern: 2 days, 2 nights, 4 days off . 12-hour shifts, including weekends and bank holidays. Cleanroom-based working environment. SCBA use required; training and relevant assessments provided. Forklift training can be provided. Due to the rural location, a full UK driving licence and access to your own transport are essential . This is an excellent opportunity to work with cutting-edge technology in a highly specialised engineering environment, with strong career development opportunities and an excellent benefits package.
Our client, a leading entity in the defence and security manufacturing sector, is looking for an Optical Assembly Build Technician to join their dynamic new team in Farnborough. This full-time, permanent role offers an exciting opportunity to work on cutting-edge defence technology and innovations, contributing to future-defining projects. You will be integral to delivering high-performance optical and optomechanical products that support advanced technologies in demanding applications. Key Responsibilities: Assemble, integrate and test precision optical and optomechanical products in accordance with engineering drawings, work instructions, and production requirements Carry out optical alignment activities using specialised equipment, including lasers, alignment telescopes, and autocollimators Perform mechanical and optical inspections using precision measurement equipment to ensure products meet quality and compliance standards Maintain accurate manufacturing records, production documentation, and traceability within ERP/MRP and electronic production systems Support troubleshooting, root cause investigations, and continuous improvement activities to optimise product quality and manufacturing efficiency Collaborate within a multidisciplinary team while adhering to cleanroom procedures, health & safety requirements, and contamination control standards Job Requirements: Extensive experience in the assembly, integration, and testing of precision optomechanical assemblies Proven ability to manufacture and assemble optomechanical products to specification using engineering drawings, work instructions, and electronic production systems Experience in carrying out optical alignment, integration, and verification activities on precision optical and mechanical systems Previous experience in an optomechanical, photonics, aerospace, defence, scientific instrumentation, or advanced manufacturing environment Experience working within cleanrooms and controlled manufacturing environments, adhering to quality and safety standards Experience using quality control processes, inspection methods, and revision-controlled manufacturing documentation Essential Qualifications: NVQ Level 3, Apprenticeship, HNC, HND or equivalent qualification in Mechanical Engineering, Manufacturing Engineering, Photonics, Physics, or a related technical discipline Evidence of formal technical training in precision manufacturing, engineering assembly or a related engineering field Demonstrable ability to interpret engineering drawings, assembly instructions, and technical documentation Proven competency in the use of precision measurement and inspection equipment within a manufacturing environment Understanding of quality standards, manufacturing documentation, and controlled production processes Commitment to working in accordance with health & safety requirements and quality management systems within a regulated manufacturing environment Benefits: Competitive salary Opportunity to work with state-of-the-art technologies Professional development and career growth opportunities Supportive and collaborative working environment Comprehensive employee benefits package If you are ready to join a cutting-edge team and have the required expertise, we encourage you to take the next step in your career. Apply now to be part of our client's innovative and forward-thinking projects at their Farnborough facility.
Aug 20, 2026
Full time
Our client, a leading entity in the defence and security manufacturing sector, is looking for an Optical Assembly Build Technician to join their dynamic new team in Farnborough. This full-time, permanent role offers an exciting opportunity to work on cutting-edge defence technology and innovations, contributing to future-defining projects. You will be integral to delivering high-performance optical and optomechanical products that support advanced technologies in demanding applications. Key Responsibilities: Assemble, integrate and test precision optical and optomechanical products in accordance with engineering drawings, work instructions, and production requirements Carry out optical alignment activities using specialised equipment, including lasers, alignment telescopes, and autocollimators Perform mechanical and optical inspections using precision measurement equipment to ensure products meet quality and compliance standards Maintain accurate manufacturing records, production documentation, and traceability within ERP/MRP and electronic production systems Support troubleshooting, root cause investigations, and continuous improvement activities to optimise product quality and manufacturing efficiency Collaborate within a multidisciplinary team while adhering to cleanroom procedures, health & safety requirements, and contamination control standards Job Requirements: Extensive experience in the assembly, integration, and testing of precision optomechanical assemblies Proven ability to manufacture and assemble optomechanical products to specification using engineering drawings, work instructions, and electronic production systems Experience in carrying out optical alignment, integration, and verification activities on precision optical and mechanical systems Previous experience in an optomechanical, photonics, aerospace, defence, scientific instrumentation, or advanced manufacturing environment Experience working within cleanrooms and controlled manufacturing environments, adhering to quality and safety standards Experience using quality control processes, inspection methods, and revision-controlled manufacturing documentation Essential Qualifications: NVQ Level 3, Apprenticeship, HNC, HND or equivalent qualification in Mechanical Engineering, Manufacturing Engineering, Photonics, Physics, or a related technical discipline Evidence of formal technical training in precision manufacturing, engineering assembly or a related engineering field Demonstrable ability to interpret engineering drawings, assembly instructions, and technical documentation Proven competency in the use of precision measurement and inspection equipment within a manufacturing environment Understanding of quality standards, manufacturing documentation, and controlled production processes Commitment to working in accordance with health & safety requirements and quality management systems within a regulated manufacturing environment Benefits: Competitive salary Opportunity to work with state-of-the-art technologies Professional development and career growth opportunities Supportive and collaborative working environment Comprehensive employee benefits package If you are ready to join a cutting-edge team and have the required expertise, we encourage you to take the next step in your career. Apply now to be part of our client's innovative and forward-thinking projects at their Farnborough facility.
Our client, a leader in the Defence & Security and Manufacturing sectors, is seeking a Principal Optical Test Technician to join their dynamic team. This permanent role is focused on supporting and developing manufacturing capabilities through detailed verification and validation processes. Key Responsibilities: Set up, align, and calibrate optical test equipment, ensuring accurate configuration and optimisation. Lead acceptance testing to ensure products meet defined optical specifications and quality standards. Implement process control techniques to maintain production consistency and perform statistical analysis for performance metrics. Work collaboratively with Optical SMEs to collate, summarise and record evidence. Produce comprehensive reports with actionable insights to refine and improve designs and processes. Oversee the transfer of test techniques and methods from R&D to mass production, ensuring scalability and repeatability. Investigate test discrepancies, implement corrective actions, and collaborate with cross-functional teams for performance enhancement. Create and maintain detailed technical documentation, including test plans, procedures, and data analysis reports. Optimise value streams and create manufacturing workflows using Lean6Sigma, TIM WOODS, and Lean methodology. Specify and implement digital production tools and capital equipment to maximise productivity and efficiency. Job Requirements: Significant experience in optical testing and a solid understanding of product manufacturing or assembly principles. Detailed understanding of risk assessments and quality standards. Excellent communication, organisational, and interpersonal skills. Strong analytical skills and experience in resolving complex issues. Proficiency in statistical data analysis and MS Office and ERP software. Knowledge of Lean and 6-sigma manufacturing principles is beneficial. Experience in the following areas is essential: fibre Laser and bulk-optic assembly testing, bulk optics handling and cleaning, using test equipment like Thermal Power meters, OSA, Scope, NI-DAQ, and PSU, alignment and adjustment of optical assemblies, and working in cleanroom environments. Understanding of product lifecycles and revision control, and experience in optical modelling and test methods. Qualifications: Bachelor's degree or higher in Industrial Engineering, Operations Management, or a related field. Advanced degrees or professional certifications in Optical Engineering, Physics, or similar are highly desirable. Or equivalent level and depth of experience and training. Benefits: Opportunity to work on complex, large-scale projects within the Defence & Security sector. Professional development and training opportunities. Collaborative and innovative work environment. Comprehensive employee benefits package. If you are an experienced Principal Optical Test Technician with a proven track record in optimising production workflows and driving production solutions, we would love to hear from you. Apply now to join our client's dedicated team.
Aug 20, 2026
Full time
Our client, a leader in the Defence & Security and Manufacturing sectors, is seeking a Principal Optical Test Technician to join their dynamic team. This permanent role is focused on supporting and developing manufacturing capabilities through detailed verification and validation processes. Key Responsibilities: Set up, align, and calibrate optical test equipment, ensuring accurate configuration and optimisation. Lead acceptance testing to ensure products meet defined optical specifications and quality standards. Implement process control techniques to maintain production consistency and perform statistical analysis for performance metrics. Work collaboratively with Optical SMEs to collate, summarise and record evidence. Produce comprehensive reports with actionable insights to refine and improve designs and processes. Oversee the transfer of test techniques and methods from R&D to mass production, ensuring scalability and repeatability. Investigate test discrepancies, implement corrective actions, and collaborate with cross-functional teams for performance enhancement. Create and maintain detailed technical documentation, including test plans, procedures, and data analysis reports. Optimise value streams and create manufacturing workflows using Lean6Sigma, TIM WOODS, and Lean methodology. Specify and implement digital production tools and capital equipment to maximise productivity and efficiency. Job Requirements: Significant experience in optical testing and a solid understanding of product manufacturing or assembly principles. Detailed understanding of risk assessments and quality standards. Excellent communication, organisational, and interpersonal skills. Strong analytical skills and experience in resolving complex issues. Proficiency in statistical data analysis and MS Office and ERP software. Knowledge of Lean and 6-sigma manufacturing principles is beneficial. Experience in the following areas is essential: fibre Laser and bulk-optic assembly testing, bulk optics handling and cleaning, using test equipment like Thermal Power meters, OSA, Scope, NI-DAQ, and PSU, alignment and adjustment of optical assemblies, and working in cleanroom environments. Understanding of product lifecycles and revision control, and experience in optical modelling and test methods. Qualifications: Bachelor's degree or higher in Industrial Engineering, Operations Management, or a related field. Advanced degrees or professional certifications in Optical Engineering, Physics, or similar are highly desirable. Or equivalent level and depth of experience and training. Benefits: Opportunity to work on complex, large-scale projects within the Defence & Security sector. Professional development and training opportunities. Collaborative and innovative work environment. Comprehensive employee benefits package. If you are an experienced Principal Optical Test Technician with a proven track record in optimising production workflows and driving production solutions, we would love to hear from you. Apply now to join our client's dedicated team.
Manufacturing Technician Location: Edinburgh (on-site) Duration: Initially until 31st March 2027 Rate: 30.81 p/h Umbrella + 30% (day) or 40% (night) shift allowance IR35: Inside Clearance: SC Cleared Overview On-site contract opportunities (x4 headcount) supporting high-precision micro-assembly/manufacturing in a controlled environment (cleanroom / temperature & humidity controlled). Working a 4 days on / 4 days off shift pattern on either days (7:00am-17:30pm) or nights (22:00pm-8:30am), you'll assemble and inspect extremely small, high-precision components using both automated machinery and manual techniques. Responsibilities: Assemble high-precision components using Automated machines, hand tools, tweezers, microscopes, or magnification systems Previous experience of Auto Assembly machines such as MRSI is preferred and/or experience of gold wire Auto bonding machines such as HESSE, Palomar or K&S. Perform fine alignment, fitting, and adjustment of components Conduct detailed visual inspections to identify defects not detectable by automated systems Follow exacting work instructions and standard operating procedures Maintain cleanroom or controlled-environment discipline where required Collaborate with quality and engineering teams to resolve precision-related issues Skillset/experience required: Good fine motor skills and hand-eye coordination Ability to manipulate extremely small parts with consistent accuracy Attention to detail and error detection Previous work in precision manufacturing, micro-assembly, electronics or similar fields Manufacturing / Production working environment (Cleanroom & Temperature and Humidity Controlled) Familiarity with precision hand tools and micro-assembly equipment
Aug 17, 2026
Contractor
Manufacturing Technician Location: Edinburgh (on-site) Duration: Initially until 31st March 2027 Rate: 30.81 p/h Umbrella + 30% (day) or 40% (night) shift allowance IR35: Inside Clearance: SC Cleared Overview On-site contract opportunities (x4 headcount) supporting high-precision micro-assembly/manufacturing in a controlled environment (cleanroom / temperature & humidity controlled). Working a 4 days on / 4 days off shift pattern on either days (7:00am-17:30pm) or nights (22:00pm-8:30am), you'll assemble and inspect extremely small, high-precision components using both automated machinery and manual techniques. Responsibilities: Assemble high-precision components using Automated machines, hand tools, tweezers, microscopes, or magnification systems Previous experience of Auto Assembly machines such as MRSI is preferred and/or experience of gold wire Auto bonding machines such as HESSE, Palomar or K&S. Perform fine alignment, fitting, and adjustment of components Conduct detailed visual inspections to identify defects not detectable by automated systems Follow exacting work instructions and standard operating procedures Maintain cleanroom or controlled-environment discipline where required Collaborate with quality and engineering teams to resolve precision-related issues Skillset/experience required: Good fine motor skills and hand-eye coordination Ability to manipulate extremely small parts with consistent accuracy Attention to detail and error detection Previous work in precision manufacturing, micro-assembly, electronics or similar fields Manufacturing / Production working environment (Cleanroom & Temperature and Humidity Controlled) Familiarity with precision hand tools and micro-assembly equipment
Inspection Technician Location: Edinburgh (on-site) Duration: Initially until 31st March 2027 Rate: 30.81 p/h Umbrella + 30% shift allowance IR35: Inside Clearance: SC Clearance required Overview An on-site contract role focused on detailed visual inspection of microelectronic components, sub-assemblies and PCBs, working to defined instructions/SOPs within a controlled manufacturing environment (cleanroom / temperature & humidity controlled). Shift pattern is 4 days on / 4 days off (7:00am-17:30pm). Responsibilities: Conduct detailed visual inspections of microelectronic components, Sub-Assemblies and PCBs to identify defects Follow work instructions and standard operating procedures Maintain cleanroom or controlled-environment discipline where required Collaborate with quality and engineering teams to resolve precision-related issues Skillset/experience required: Proven experience in electronics inspection IPC 610 certified preferable Exceptional fine motor skills and hand-eye coordination Superior attention to detail and error detection Previous work in precision manufacturing, micro-assembly, electronics or similar fields Manufacturing / Production working environment (Cleanroom & Temperature and Humidity Controlled) Familiarity with Microscope, precision hand tools and micro-assembly equipment
Aug 15, 2026
Contractor
Inspection Technician Location: Edinburgh (on-site) Duration: Initially until 31st March 2027 Rate: 30.81 p/h Umbrella + 30% shift allowance IR35: Inside Clearance: SC Clearance required Overview An on-site contract role focused on detailed visual inspection of microelectronic components, sub-assemblies and PCBs, working to defined instructions/SOPs within a controlled manufacturing environment (cleanroom / temperature & humidity controlled). Shift pattern is 4 days on / 4 days off (7:00am-17:30pm). Responsibilities: Conduct detailed visual inspections of microelectronic components, Sub-Assemblies and PCBs to identify defects Follow work instructions and standard operating procedures Maintain cleanroom or controlled-environment discipline where required Collaborate with quality and engineering teams to resolve precision-related issues Skillset/experience required: Proven experience in electronics inspection IPC 610 certified preferable Exceptional fine motor skills and hand-eye coordination Superior attention to detail and error detection Previous work in precision manufacturing, micro-assembly, electronics or similar fields Manufacturing / Production working environment (Cleanroom & Temperature and Humidity Controlled) Familiarity with Microscope, precision hand tools and micro-assembly equipment
GMP Production Manufacturing Technician Opportunity Oxford Opportunity: An exciting opportunity has been created due to company growth. My client a global pharmaceutical manufacturing company is looking to recruit a Production Manufacturing Technician based in Oxford where you will be working in a sterile GMP clean room manufacturing environment making drug products / compounding as allocated on the production planning system to cGMP and ISO standards. The hours of work are 37.5 hours per week on a weekly rotating shift pattern of 7:00 am 3:00 pm 1 week and then 10:00 am 6:00 pm for 1 week (Monday to Friday). Duties and Responsibilities include: Working in a controlled cleanroom environment using manufacturing equipment and computer systems. Collaborating with a team to produce high-quality medical products. Meeting tight production deadlines whilst maintaining accuracy and compliance. Carrying out environmental monitoring activities. Performing routine quality checks throughout the compounding process. Accurately completing and managing production documentation in line with Good Documentation Practices (GDP). Supporting various stages of manufacturing such as labelling, visual inspection, picking, preparation, and sanitization. As you will be working in a sterile clean room no make or jewellery is allowed. This is a 12 months contract which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance. The PAYE rate is £16.17 per hour. Skills: To apply for the role of GMP Production Manufacturing Technician Nights you will have the following: GCSE English and Maths Grade C or above. Ideally pharmaceutical / medical device GMP production / manufacturing / operator experience, in a clean room environment but flexible on this. PC literate and numerate. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Aug 08, 2026
Contractor
GMP Production Manufacturing Technician Opportunity Oxford Opportunity: An exciting opportunity has been created due to company growth. My client a global pharmaceutical manufacturing company is looking to recruit a Production Manufacturing Technician based in Oxford where you will be working in a sterile GMP clean room manufacturing environment making drug products / compounding as allocated on the production planning system to cGMP and ISO standards. The hours of work are 37.5 hours per week on a weekly rotating shift pattern of 7:00 am 3:00 pm 1 week and then 10:00 am 6:00 pm for 1 week (Monday to Friday). Duties and Responsibilities include: Working in a controlled cleanroom environment using manufacturing equipment and computer systems. Collaborating with a team to produce high-quality medical products. Meeting tight production deadlines whilst maintaining accuracy and compliance. Carrying out environmental monitoring activities. Performing routine quality checks throughout the compounding process. Accurately completing and managing production documentation in line with Good Documentation Practices (GDP). Supporting various stages of manufacturing such as labelling, visual inspection, picking, preparation, and sanitization. As you will be working in a sterile clean room no make or jewellery is allowed. This is a 12 months contract which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance. The PAYE rate is £16.17 per hour. Skills: To apply for the role of GMP Production Manufacturing Technician Nights you will have the following: GCSE English and Maths Grade C or above. Ideally pharmaceutical / medical device GMP production / manufacturing / operator experience, in a clean room environment but flexible on this. PC literate and numerate. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
At OQC, we aren't just theorising about the future; we're building it. Born from a philosophy of bold innovation, we've successfully transitioned quantum computing from an academic dream into a commercial reality. The most exciting thing is that we're just getting started and we've recently closed our £260 million Series C funding round - the largest fundraise ever completed by a quantum computing company in Europe. The Purpose As our Cleanroom Operations Manager, you'll lead the day-to-day operation of OQC's cleanroom as we scale the manufacture of world-leading quantum technologies. You'll build the operational discipline, team capability and processes that enable safe, reliable and efficient fabrication while supporting the next generation of quantum hardware. The Role Leading a team of engineers and technicians, you'll oversee cleanroom operations, equipment readiness, maintenance planning and operational excellence. Working closely with engineering, quality, facilities, supply chain and programme teams, you'll ensure our fabrication environment operates safely, efficiently and is ready to support increasing production demands. What You'll Be Working On Lead the day-to-day operation of OQC's cleanroom, ensuring resources, equipment and priorities are aligned to fabrication goals. Manage, coach and develop a team of engineers and technicians, supporting performance, capability growth and operational excellence. Coordinate equipment readiness, maintenance, consumables and inventory to maximise uptime and minimise disruption. Monitor operational KPIs, identify delivery risks and drive continuous improvements in reliability, throughput, quality and safety. Maintain robust operational procedures, documentation, SOPs and traceability to support controlled fabrication processes. Collaborate with engineering, facilities, quality, supply chain and programme teams to ensure operational readiness and successful delivery. Support the continued industrialisation of OQC's fabrication capability by improving scheduling, operational controls and team effectiveness. What We're Looking For Experience leading operations within a cleanroom, semiconductor manufacturing, fabrication, production or other critical technical environment. Experience managing or leading engineers, technicians or operational teams, including coaching, task allocation and performance management. Strong experience coordinating production schedules, equipment readiness and maintenance activities in complex technical environments. Experience using operational KPIs to improve reliability, utilisation, throughput and delivery performance. Experience working with SOPs, controlled documentation, traceability requirements and operational processes. Strong planning, stakeholder management and organisational skills, with the ability to balance competing priorities. Commitment to safety, quality and continuous improvement. Bachelor's degree in Engineering, Physics, Microelectronics, Semiconductor Manufacturing, Production Management or a related discipline. The 'Nice-to-Haves' Experience supporting industrialisation, production ramp-up or operational excellence programmes. Master's degree in Engineering, Physics, Microelectronics, Semiconductor Manufacturing, Production Management or a related discipline.
Aug 08, 2026
Full time
At OQC, we aren't just theorising about the future; we're building it. Born from a philosophy of bold innovation, we've successfully transitioned quantum computing from an academic dream into a commercial reality. The most exciting thing is that we're just getting started and we've recently closed our £260 million Series C funding round - the largest fundraise ever completed by a quantum computing company in Europe. The Purpose As our Cleanroom Operations Manager, you'll lead the day-to-day operation of OQC's cleanroom as we scale the manufacture of world-leading quantum technologies. You'll build the operational discipline, team capability and processes that enable safe, reliable and efficient fabrication while supporting the next generation of quantum hardware. The Role Leading a team of engineers and technicians, you'll oversee cleanroom operations, equipment readiness, maintenance planning and operational excellence. Working closely with engineering, quality, facilities, supply chain and programme teams, you'll ensure our fabrication environment operates safely, efficiently and is ready to support increasing production demands. What You'll Be Working On Lead the day-to-day operation of OQC's cleanroom, ensuring resources, equipment and priorities are aligned to fabrication goals. Manage, coach and develop a team of engineers and technicians, supporting performance, capability growth and operational excellence. Coordinate equipment readiness, maintenance, consumables and inventory to maximise uptime and minimise disruption. Monitor operational KPIs, identify delivery risks and drive continuous improvements in reliability, throughput, quality and safety. Maintain robust operational procedures, documentation, SOPs and traceability to support controlled fabrication processes. Collaborate with engineering, facilities, quality, supply chain and programme teams to ensure operational readiness and successful delivery. Support the continued industrialisation of OQC's fabrication capability by improving scheduling, operational controls and team effectiveness. What We're Looking For Experience leading operations within a cleanroom, semiconductor manufacturing, fabrication, production or other critical technical environment. Experience managing or leading engineers, technicians or operational teams, including coaching, task allocation and performance management. Strong experience coordinating production schedules, equipment readiness and maintenance activities in complex technical environments. Experience using operational KPIs to improve reliability, utilisation, throughput and delivery performance. Experience working with SOPs, controlled documentation, traceability requirements and operational processes. Strong planning, stakeholder management and organisational skills, with the ability to balance competing priorities. Commitment to safety, quality and continuous improvement. Bachelor's degree in Engineering, Physics, Microelectronics, Semiconductor Manufacturing, Production Management or a related discipline. The 'Nice-to-Haves' Experience supporting industrialisation, production ramp-up or operational excellence programmes. Master's degree in Engineering, Physics, Microelectronics, Semiconductor Manufacturing, Production Management or a related discipline.
GMP Production Manufacturing Technician Opportunity Oxford Opportunity: An exciting opportunity has been created due to company growth. My client a global pharmaceutical manufacturing company is looking to recruit a Production Manufacturing Technician based in Oxford where you will be working in a sterile GMP clean room manufacturing environment making drug products / compounding as allocated on the production planning system to cGMP and ISO standards. The hours of work are 37.5 hours per week on a weekly rotating shift pattern of 7:00 am 3:00 pm 1 week and then 10:00 am 6:00 pm for 1 week (Monday to Friday). Duties and Responsibilities include: Working in a controlled cleanroom environment using manufacturing equipment and computer systems. Collaborating with a team to produce high-quality medical products. Meeting tight production deadlines whilst maintaining accuracy and compliance. Carrying out environmental monitoring activities. Performing routine quality checks throughout the compounding process. Accurately completing and managing production documentation in line with Good Documentation Practices (GDP). Supporting various stages of manufacturing such as labelling, visual inspection, picking, preparation, and sanitization. As you will be working in a sterile clean room no make or jewellery is allowed. This is a 12 months contract which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance. The PAYE rate is £16.17 per hour. Skills: To apply for the role of GMP Production Manufacturing Technician Nights you will have the following: GCSE English and Maths Grade C or above. Ideally pharmaceutical / medical device GMP production / manufacturing / operator experience, in a clean room environment but flexible on this. PC literate and numerate. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
Aug 08, 2026
Contractor
GMP Production Manufacturing Technician Opportunity Oxford Opportunity: An exciting opportunity has been created due to company growth. My client a global pharmaceutical manufacturing company is looking to recruit a Production Manufacturing Technician based in Oxford where you will be working in a sterile GMP clean room manufacturing environment making drug products / compounding as allocated on the production planning system to cGMP and ISO standards. The hours of work are 37.5 hours per week on a weekly rotating shift pattern of 7:00 am 3:00 pm 1 week and then 10:00 am 6:00 pm for 1 week (Monday to Friday). Duties and Responsibilities include: Working in a controlled cleanroom environment using manufacturing equipment and computer systems. Collaborating with a team to produce high-quality medical products. Meeting tight production deadlines whilst maintaining accuracy and compliance. Carrying out environmental monitoring activities. Performing routine quality checks throughout the compounding process. Accurately completing and managing production documentation in line with Good Documentation Practices (GDP). Supporting various stages of manufacturing such as labelling, visual inspection, picking, preparation, and sanitization. As you will be working in a sterile clean room no make or jewellery is allowed. This is a 12 months contract which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance. The PAYE rate is £16.17 per hour. Skills: To apply for the role of GMP Production Manufacturing Technician Nights you will have the following: GCSE English and Maths Grade C or above. Ideally pharmaceutical / medical device GMP production / manufacturing / operator experience, in a clean room environment but flexible on this. PC literate and numerate. How to Apply: To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website. If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information. For a list of our current vacancies, please visit the Quality Start website. If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role. Quality Start are acting as a specialist recruitment consultancy for this role.
OQC in Reading, UK, is building the next generation of quantum hardware. As Cleanroom Operations Manager, you will lead daily cleanroom activity, align resources and priorities with fabrication goals, and ensure safe, reliable manufacturing of world-leading technologies. You will manage engineers and technicians, drive improvements in uptime, throughput and quality, and collaborate across engineering, quality, facilities and supply chain to industrialise our fabrication capability.
Aug 08, 2026
Full time
OQC in Reading, UK, is building the next generation of quantum hardware. As Cleanroom Operations Manager, you will lead daily cleanroom activity, align resources and priorities with fabrication goals, and ensure safe, reliable manufacturing of world-leading technologies. You will manage engineers and technicians, drive improvements in uptime, throughput and quality, and collaborate across engineering, quality, facilities and supply chain to industrialise our fabrication capability.
Oxford Quantum Circuits is seeking a Cleanroom Operations Manager to lead the day-to-day operations of its cleanroom as the team scales fabrication of world-leading quantum technologies. You will build operational discipline, team capability and processes to ensure safe, reliable, and efficient manufacturing while supporting next-generation hardware. You will oversee engineers and technicians, coordinate equipment readiness and maintenance, and collaborate with engineering, quality, facilities
Aug 06, 2026
Full time
Oxford Quantum Circuits is seeking a Cleanroom Operations Manager to lead the day-to-day operations of its cleanroom as the team scales fabrication of world-leading quantum technologies. You will build operational discipline, team capability and processes to ensure safe, reliable, and efficient manufacturing while supporting next-generation hardware. You will oversee engineers and technicians, coordinate equipment readiness and maintenance, and collaborate with engineering, quality, facilities
At OQC, we aren't just theorising about the future; we're building it. Born from a philosophy of bold innovation, we've successfully transitioned quantum computing from an academic dream into a commercial reality. The most exciting thing is that we're just getting started and we've recently closed our £260 million Series C funding round - the largest fundraise ever completed by a quantum computing company in Europe. The Purpose As our Cleanroom Operations Manager, you'll lead the day-to-day operation of OQC's cleanroom as we scale the manufacture of world-leading quantum technologies. You'll build the operational discipline, team capability and processes that enable safe, reliable and efficient fabrication while supporting the next generation of quantum hardware. The Role Leading a team of engineers and technicians, you'll oversee cleanroom operations, equipment readiness, maintenance planning and operational excellence. Working closely with engineering, quality, facilities, supply chain and programme teams, you'll ensure our fabrication environment operates safely, efficiently and is ready to support increasing production demands. What You'll Be Working On Lead the day-to-day operation of OQC's cleanroom, ensuring resources, equipment and priorities are aligned to fabrication goals. Manage, coach and develop a team of engineers and technicians, supporting performance, capability growth and operational excellence. Coordinate equipment readiness, maintenance, consumables and inventory to maximise uptime and minimise disruption. Monitor operational KPIs, identify delivery risks and drive continuous improvements in reliability, throughput, quality and safety. Maintain robust operational procedures, documentation, SOPs and traceability to support controlled fabrication processes. Collaborate with engineering, facilities, quality, supply chain and programme teams to ensure operational readiness and successful delivery. Support the continued industrialisation of OQC's fabrication capability by improving scheduling, operational controls and team effectiveness. What We're Looking For Experience leading operations within a cleanroom, semiconductor manufacturing, fabrication, production or other critical technical environment. Experience managing or leading engineers, technicians or operational teams, including coaching, task allocation and performance management. Strong experience coordinating production schedules, equipment readiness and maintenance activities in complex technical environments. Experience using operational KPIs to improve reliability, utilisation, throughput and delivery performance. Experience working with SOPs, controlled documentation, traceability requirements and operational processes. Strong planning, stakeholder management and organisational skills, with the ability to balance competing priorities. Commitment to safety, quality and continuous improvement. Bachelor's degree in Engineering, Physics, Microelectronics, Semiconductor Manufacturing, Production Management or a related discipline. The 'Nice-to-Haves' Experience supporting industrialisation, production ramp-up or operational excellence programmes. Master's degree in Engineering, Physics, Microelectronics, Semiconductor Manufacturing, Production Management or a related discipline.
Aug 06, 2026
Full time
At OQC, we aren't just theorising about the future; we're building it. Born from a philosophy of bold innovation, we've successfully transitioned quantum computing from an academic dream into a commercial reality. The most exciting thing is that we're just getting started and we've recently closed our £260 million Series C funding round - the largest fundraise ever completed by a quantum computing company in Europe. The Purpose As our Cleanroom Operations Manager, you'll lead the day-to-day operation of OQC's cleanroom as we scale the manufacture of world-leading quantum technologies. You'll build the operational discipline, team capability and processes that enable safe, reliable and efficient fabrication while supporting the next generation of quantum hardware. The Role Leading a team of engineers and technicians, you'll oversee cleanroom operations, equipment readiness, maintenance planning and operational excellence. Working closely with engineering, quality, facilities, supply chain and programme teams, you'll ensure our fabrication environment operates safely, efficiently and is ready to support increasing production demands. What You'll Be Working On Lead the day-to-day operation of OQC's cleanroom, ensuring resources, equipment and priorities are aligned to fabrication goals. Manage, coach and develop a team of engineers and technicians, supporting performance, capability growth and operational excellence. Coordinate equipment readiness, maintenance, consumables and inventory to maximise uptime and minimise disruption. Monitor operational KPIs, identify delivery risks and drive continuous improvements in reliability, throughput, quality and safety. Maintain robust operational procedures, documentation, SOPs and traceability to support controlled fabrication processes. Collaborate with engineering, facilities, quality, supply chain and programme teams to ensure operational readiness and successful delivery. Support the continued industrialisation of OQC's fabrication capability by improving scheduling, operational controls and team effectiveness. What We're Looking For Experience leading operations within a cleanroom, semiconductor manufacturing, fabrication, production or other critical technical environment. Experience managing or leading engineers, technicians or operational teams, including coaching, task allocation and performance management. Strong experience coordinating production schedules, equipment readiness and maintenance activities in complex technical environments. Experience using operational KPIs to improve reliability, utilisation, throughput and delivery performance. Experience working with SOPs, controlled documentation, traceability requirements and operational processes. Strong planning, stakeholder management and organisational skills, with the ability to balance competing priorities. Commitment to safety, quality and continuous improvement. Bachelor's degree in Engineering, Physics, Microelectronics, Semiconductor Manufacturing, Production Management or a related discipline. The 'Nice-to-Haves' Experience supporting industrialisation, production ramp-up or operational excellence programmes. Master's degree in Engineering, Physics, Microelectronics, Semiconductor Manufacturing, Production Management or a related discipline.
Sekisui Diagnostics in Maidstone, UK, is seeking a QC Technician III (Microbiology) to join the QC department on a full-time basis. You will perform inspections, check testing and sampling for manufacturing processes, assist with validation or troubleshooting of testing methods and work across QC Microbiology labs and GMP cleanrooms. The successful candidate will have aseptic technique experience, microbiology lab knowledge, and strong IT skills.
Jul 31, 2026
Full time
Sekisui Diagnostics in Maidstone, UK, is seeking a QC Technician III (Microbiology) to join the QC department on a full-time basis. You will perform inspections, check testing and sampling for manufacturing processes, assist with validation or troubleshooting of testing methods and work across QC Microbiology labs and GMP cleanrooms. The successful candidate will have aseptic technique experience, microbiology lab knowledge, and strong IT skills.
Kent UK Liphook Way Allington Maidstone, ME160Q, GBR Kent UK Liphook Way Allington Maidstone, ME160Q, GBR We are looking to appoint a QC Technician III (Microbiology) to join the QC department on a full time basis. As part of a dedicated team, you will perform inspections, check testing and sampling procedures for product manufacturing processes. You will carry out packaging line, manufacturing inspections and sampling and testing of incoming components and raw materials to ensure that company standards are met. You may assist with validating or troubleshooting testing methods, including assays. To be a successful in this role, you will perform an array of microbiological environmental sampling, such as active air, passive air, surface bioburden and non-viable particulate monitoring. You will also perform microbiological sampling and testing of site utilities such as purified water, compressed gases and pure steam, along with microbial testing, including but not limited to bioburden assessment using filtration; detection of endotoxin; basic identification of microorganisms; media growth promotion, etc. You will work in a variety of business units, such as the QC Microbiology laboratory, production environments, and GMP cleanrooms. You will keep accurate and detailed records of all laboratory work in accordance with company procedures; completion of Good Manufacturing Practices (GMP) testing paperwork to a high specification in line with ALCOA (Attributable, Legible, Contemporaneous, Original and Accurate) expectations. You will ensure laboratory media, chemicals and consumables are stocked to prevent testing delays. You will ensure equipment, instruments, and facilities within the laboratory are calibrated, and kept serviceable. You will ensure all QC working practices are in compliance with the requirements of EudraLex v. 4, where required. The successful candidate will have education and / or experience in some, or all, of the following areas: 8 years relevant work experience or associate degree with 3-5 years relevant work experience or Bachelor's degree with 1-2 years relevant experience preferred Proficient in aseptic technique and experience of working in a QC Microbiology laboratory A degree of familiarity of sampling within production and cleanrooms Diligent and with a meticulous approach to all tasks, with a keen eye for detail Good IT skills e.g. Microsoft Office (Word, Excel and Outlook) Strong analytical and problem solving ability Good planning, organizational, and time management skills Experience in Kaizen/Lean/Sigma an asset About us: At Sekisui Diagnostics, we help improve patient outcomes by doing what we've always done - focusing on innovating and developing highly accurate diagnostics tests, reagents, and systems. In recent years, social and consumer needs for medical care have been diversifying in line with dramatic transformations in the global medical environment. We will continue to embrace change and challenge new frontiers so that we can create unique, high-quality products and services that will leave our customers truly satisfied. With worldwide state-of-the-art manufacturing facilities and an international sales and distribution network, we are a solid partner for healthcare professionals, distributors, and manufacturers around the world. Our global capabilities allow us to meet the specific needs of our wide range of customers - and customize solutions at both a regional and product level. As an equal opportunity employer, Sekisui Diagnostics is committed to a diverse workforce. Employment decisions will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, other non-job-related characteristics, or other prohibited grounds specified in applicable country and local laws. It is also Sekisui Diagnostics policy to comply with all applicable country and local laws respecting consideration of unemployment status in making hiring decisions. Sekisui Diagnostics is pleased to consider all qualified applicants for open roles and only those candidates who are selected for further consideration or interviews will be contacted by a member of the Company's internal recruiting team.
Jul 31, 2026
Full time
Kent UK Liphook Way Allington Maidstone, ME160Q, GBR Kent UK Liphook Way Allington Maidstone, ME160Q, GBR We are looking to appoint a QC Technician III (Microbiology) to join the QC department on a full time basis. As part of a dedicated team, you will perform inspections, check testing and sampling procedures for product manufacturing processes. You will carry out packaging line, manufacturing inspections and sampling and testing of incoming components and raw materials to ensure that company standards are met. You may assist with validating or troubleshooting testing methods, including assays. To be a successful in this role, you will perform an array of microbiological environmental sampling, such as active air, passive air, surface bioburden and non-viable particulate monitoring. You will also perform microbiological sampling and testing of site utilities such as purified water, compressed gases and pure steam, along with microbial testing, including but not limited to bioburden assessment using filtration; detection of endotoxin; basic identification of microorganisms; media growth promotion, etc. You will work in a variety of business units, such as the QC Microbiology laboratory, production environments, and GMP cleanrooms. You will keep accurate and detailed records of all laboratory work in accordance with company procedures; completion of Good Manufacturing Practices (GMP) testing paperwork to a high specification in line with ALCOA (Attributable, Legible, Contemporaneous, Original and Accurate) expectations. You will ensure laboratory media, chemicals and consumables are stocked to prevent testing delays. You will ensure equipment, instruments, and facilities within the laboratory are calibrated, and kept serviceable. You will ensure all QC working practices are in compliance with the requirements of EudraLex v. 4, where required. The successful candidate will have education and / or experience in some, or all, of the following areas: 8 years relevant work experience or associate degree with 3-5 years relevant work experience or Bachelor's degree with 1-2 years relevant experience preferred Proficient in aseptic technique and experience of working in a QC Microbiology laboratory A degree of familiarity of sampling within production and cleanrooms Diligent and with a meticulous approach to all tasks, with a keen eye for detail Good IT skills e.g. Microsoft Office (Word, Excel and Outlook) Strong analytical and problem solving ability Good planning, organizational, and time management skills Experience in Kaizen/Lean/Sigma an asset About us: At Sekisui Diagnostics, we help improve patient outcomes by doing what we've always done - focusing on innovating and developing highly accurate diagnostics tests, reagents, and systems. In recent years, social and consumer needs for medical care have been diversifying in line with dramatic transformations in the global medical environment. We will continue to embrace change and challenge new frontiers so that we can create unique, high-quality products and services that will leave our customers truly satisfied. With worldwide state-of-the-art manufacturing facilities and an international sales and distribution network, we are a solid partner for healthcare professionals, distributors, and manufacturers around the world. Our global capabilities allow us to meet the specific needs of our wide range of customers - and customize solutions at both a regional and product level. As an equal opportunity employer, Sekisui Diagnostics is committed to a diverse workforce. Employment decisions will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, other non-job-related characteristics, or other prohibited grounds specified in applicable country and local laws. It is also Sekisui Diagnostics policy to comply with all applicable country and local laws respecting consideration of unemployment status in making hiring decisions. Sekisui Diagnostics is pleased to consider all qualified applicants for open roles and only those candidates who are selected for further consideration or interviews will be contacted by a member of the Company's internal recruiting team.
At OQC, we aren't just theorising about the future; we're building it. Born from a philosophy of bold innovation, we've successfully transitioned quantum computing from an academic dream into a commercial reality. The most exciting thing is that we're just getting started. The Mission As a Nanofabrication Technician, you'll play a critical role in supporting the smooth, safe, and efficient operation of our nanofabrication laboratory. Working closely with our Nanofabrication Engineers, you'll help maintain the high operational standards required to fabricate next generation superconducting quantum devices. You'll be hands on in the lab environment, ensuring equipment, materials, and processes are prepared and maintained to enable world class experimental outcomes. The Role You'll join the Materials Science & Device Engineering team, supporting the day to day running of our nanofabrication facilities and contributing to the production of cutting edge electronic superconductor devices. What You'll Be Working On Supporting the daily operation of the fabrication lab, including preparing wafers, glassware, solutions, and experimental setups Maintaining cleanroom and laboratory standards to ensure a safe, organised, and efficient working environment Monitoring stock levels, consumables, and equipment supplies to ensure uninterrupted lab operations Supporting fabrication processes including wafer cleaning, resist spinning, photolithography, etching, and deposition monitoring Performing quality assurance checks on internally and externally fabricated wafers, documenting and reporting findings Following and contributing to health & safety procedures, chemical handling standards, and laboratory best practices Documenting experimental work, process observations, and operational activities in line with team standards What We're Looking For Experience working in a laboratory or cleanroom environment Strong attention to detail and excellent manual dexterity when handling delicate materials and equipment Ability to follow strict health & safety and chemical handling procedures Experience maintaining accurate laboratory documentation and records Organised and proactive approach to managing workloads and priorities Strong time management skills with the ability to work independently Comfortable supporting scientific or engineering experimental processes Self motivated with a collaborative mindset and willingness to continuously improve processes The 'Nice-to-Haves' Experience working within nanofabrication environments Experience with stock control and laboratory inventory management Familiarity with superconducting device fabrication processes Experience writing or contributing to risk assessments and H&S procedures Degree or equivalent qualification in Science, Engineering, or a related discipline Experience planning or devising scientific experiments Why Join OQC You will join a world class team at the forefront of the next computational era. We offer a culture of bold innovation, the chance to work with unique lab infrastructure, and the opportunity to see your work redefine the limits of computation.
Jul 31, 2026
Full time
At OQC, we aren't just theorising about the future; we're building it. Born from a philosophy of bold innovation, we've successfully transitioned quantum computing from an academic dream into a commercial reality. The most exciting thing is that we're just getting started. The Mission As a Nanofabrication Technician, you'll play a critical role in supporting the smooth, safe, and efficient operation of our nanofabrication laboratory. Working closely with our Nanofabrication Engineers, you'll help maintain the high operational standards required to fabricate next generation superconducting quantum devices. You'll be hands on in the lab environment, ensuring equipment, materials, and processes are prepared and maintained to enable world class experimental outcomes. The Role You'll join the Materials Science & Device Engineering team, supporting the day to day running of our nanofabrication facilities and contributing to the production of cutting edge electronic superconductor devices. What You'll Be Working On Supporting the daily operation of the fabrication lab, including preparing wafers, glassware, solutions, and experimental setups Maintaining cleanroom and laboratory standards to ensure a safe, organised, and efficient working environment Monitoring stock levels, consumables, and equipment supplies to ensure uninterrupted lab operations Supporting fabrication processes including wafer cleaning, resist spinning, photolithography, etching, and deposition monitoring Performing quality assurance checks on internally and externally fabricated wafers, documenting and reporting findings Following and contributing to health & safety procedures, chemical handling standards, and laboratory best practices Documenting experimental work, process observations, and operational activities in line with team standards What We're Looking For Experience working in a laboratory or cleanroom environment Strong attention to detail and excellent manual dexterity when handling delicate materials and equipment Ability to follow strict health & safety and chemical handling procedures Experience maintaining accurate laboratory documentation and records Organised and proactive approach to managing workloads and priorities Strong time management skills with the ability to work independently Comfortable supporting scientific or engineering experimental processes Self motivated with a collaborative mindset and willingness to continuously improve processes The 'Nice-to-Haves' Experience working within nanofabrication environments Experience with stock control and laboratory inventory management Familiarity with superconducting device fabrication processes Experience writing or contributing to risk assessments and H&S procedures Degree or equivalent qualification in Science, Engineering, or a related discipline Experience planning or devising scientific experiments Why Join OQC You will join a world class team at the forefront of the next computational era. We offer a culture of bold innovation, the chance to work with unique lab infrastructure, and the opportunity to see your work redefine the limits of computation.
At OQC, we aren't just theorising about the future; we're building it. Born from a philosophy of bold innovation, we've successfully transitioned quantum computing from an academic dream into a commercial reality. The most exciting thing is that we're just getting started. The Mission As a Nanofabrication Technician, you'll play a critical role in supporting the smooth, safe, and efficient operation of our nanofabrication laboratory. Working closely with our Nanofabrication Engineers, you'll help maintain the high operational standards required to fabricate next-generation superconducting quantum devices. You'll be hands-on in the lab environment, ensuring equipment, materials, and processes are prepared and maintained to enable world-class experimental outcomes. The Role You'll join the Materials Science & Device Engineering team, supporting the day-to-day running of our nanofabrication facilities and contributing to the production of cutting-edge electronic superconductor devices. What You'll Be Working On Supporting the daily operation of the fabrication lab, including preparing wafers, glassware, solutions, and experimental setups Maintaining cleanroom and laboratory standards to ensure a safe, organised, and efficient working environment Monitoring stock levels, consumables, and equipment supplies to ensure uninterrupted lab operations Supporting fabrication processes including wafer cleaning, resist spinning, photolithography, etching, and deposition monitoring Performing quality assurance checks on internally and externally fabricated wafers, documenting and reporting findings Following and contributing to health & safety procedures, chemical handling standards, and laboratory best practices Documenting experimental work, process observations, and operational activities in line with team standards What We're Looking For Experience working in a laboratory or cleanroom environment Strong attention to detail and excellent manual dexterity when handling delicate materials and equipment Ability to follow strict health & safety and chemical handling procedures Experience maintaining accurate laboratory documentation and records Organised and proactive approach to managing workloads and priorities Strong time management skills with the ability to work independently Comfortable supporting scientific or engineering experimental processes Self-motivated with a collaborative mindset and willingness to continuously improve processes The 'Nice-to-Haves' Experience working within nanofabrication environments Experience with stock control and laboratory inventory management Familiarity with superconducting device fabrication processes Experience writing or contributing to risk assessments and H&S procedures Degree or equivalent qualification in Science, Engineering, or a related discipline Experience planning or devising scientific experiments Why Join OQC You will join a world-class team at the forefront of the next computational era. We offer a culture of bold innovation, the chance to work with unique lab infrastructure, and the opportunity to see your work redefine the limits of computation. Learn more about our benefits and positive work culture here:
Jul 31, 2026
Full time
At OQC, we aren't just theorising about the future; we're building it. Born from a philosophy of bold innovation, we've successfully transitioned quantum computing from an academic dream into a commercial reality. The most exciting thing is that we're just getting started. The Mission As a Nanofabrication Technician, you'll play a critical role in supporting the smooth, safe, and efficient operation of our nanofabrication laboratory. Working closely with our Nanofabrication Engineers, you'll help maintain the high operational standards required to fabricate next-generation superconducting quantum devices. You'll be hands-on in the lab environment, ensuring equipment, materials, and processes are prepared and maintained to enable world-class experimental outcomes. The Role You'll join the Materials Science & Device Engineering team, supporting the day-to-day running of our nanofabrication facilities and contributing to the production of cutting-edge electronic superconductor devices. What You'll Be Working On Supporting the daily operation of the fabrication lab, including preparing wafers, glassware, solutions, and experimental setups Maintaining cleanroom and laboratory standards to ensure a safe, organised, and efficient working environment Monitoring stock levels, consumables, and equipment supplies to ensure uninterrupted lab operations Supporting fabrication processes including wafer cleaning, resist spinning, photolithography, etching, and deposition monitoring Performing quality assurance checks on internally and externally fabricated wafers, documenting and reporting findings Following and contributing to health & safety procedures, chemical handling standards, and laboratory best practices Documenting experimental work, process observations, and operational activities in line with team standards What We're Looking For Experience working in a laboratory or cleanroom environment Strong attention to detail and excellent manual dexterity when handling delicate materials and equipment Ability to follow strict health & safety and chemical handling procedures Experience maintaining accurate laboratory documentation and records Organised and proactive approach to managing workloads and priorities Strong time management skills with the ability to work independently Comfortable supporting scientific or engineering experimental processes Self-motivated with a collaborative mindset and willingness to continuously improve processes The 'Nice-to-Haves' Experience working within nanofabrication environments Experience with stock control and laboratory inventory management Familiarity with superconducting device fabrication processes Experience writing or contributing to risk assessments and H&S procedures Degree or equivalent qualification in Science, Engineering, or a related discipline Experience planning or devising scientific experiments Why Join OQC You will join a world-class team at the forefront of the next computational era. We offer a culture of bold innovation, the chance to work with unique lab infrastructure, and the opportunity to see your work redefine the limits of computation. Learn more about our benefits and positive work culture here:
Randstad Construction & Property
Cramlington, Northumberland
Manufacturing Technician I Location: Cramlington Position Type: Full-Time, 12-Month Contract Shift Pattern: 4 Days On - 4 Days Off (18:00 - 06:00) Pay Rate: 13.46 per hour + 30% Shift Allowance The Role We are looking for a dedicated Manufacturing Technician to join our production team in Cramlington. In this role, you will work within a cGMP-compliant cleanroom environment to safely and efficiently assemble high-quality single-use medical products. This is a vital position that ensures our products meet stringent quality standards to fulfill critical customer orders worldwide. Key Responsibilities Manual Assembly: Assemble material components using manual, electronic, and pneumatic hand tools according to detailed drawings and SOPs. Quality Control: Maintain 5S standards and ensure all products are cGMP compliant. Documentation: Accurately record critical data within batch records. Preparation: Handle critical components and set up/kit raw materials for production. Safety: Follow all safe working practices and utilize required PPE at all times. Requirements Physical Stamina: Ability to stand for the duration of a 12-hour shift and perform lifting/carrying tasks. Technical Aptitude: Experience using hand tools and the ability to read technical drawings. Detail Oriented: Good eyesight for inspecting finished goods and basic mathematical skills for data recording. Reliability: A punctual, dependable work ethic and a flexible approach to changing production needs. Experience: Previous experience in a cleanroom or manufacturing assembly environment is preferred but not essential. Apply today! Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application. Candidates must be eligible to live and work in the UK. For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
Jun 03, 2026
Contractor
Manufacturing Technician I Location: Cramlington Position Type: Full-Time, 12-Month Contract Shift Pattern: 4 Days On - 4 Days Off (18:00 - 06:00) Pay Rate: 13.46 per hour + 30% Shift Allowance The Role We are looking for a dedicated Manufacturing Technician to join our production team in Cramlington. In this role, you will work within a cGMP-compliant cleanroom environment to safely and efficiently assemble high-quality single-use medical products. This is a vital position that ensures our products meet stringent quality standards to fulfill critical customer orders worldwide. Key Responsibilities Manual Assembly: Assemble material components using manual, electronic, and pneumatic hand tools according to detailed drawings and SOPs. Quality Control: Maintain 5S standards and ensure all products are cGMP compliant. Documentation: Accurately record critical data within batch records. Preparation: Handle critical components and set up/kit raw materials for production. Safety: Follow all safe working practices and utilize required PPE at all times. Requirements Physical Stamina: Ability to stand for the duration of a 12-hour shift and perform lifting/carrying tasks. Technical Aptitude: Experience using hand tools and the ability to read technical drawings. Detail Oriented: Good eyesight for inspecting finished goods and basic mathematical skills for data recording. Reliability: A punctual, dependable work ethic and a flexible approach to changing production needs. Experience: Previous experience in a cleanroom or manufacturing assembly environment is preferred but not essential. Apply today! Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application. Candidates must be eligible to live and work in the UK. For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
Location: Melbourn, near Royston (SG8) Type of Work: Temporary Duration: 3 months initially, option to transfer to permanent staff for the right candidates Hours: 8am - 4.30pm, Monday to Friday (37.5 hour week) Will move to early / late shift in due course (6am - 2:30pm and 1:30pm - 10pm on a weekly rotation) Salary: £17 per hour Job Reference: 36151 Polytec are looking for Cleanroom Technicians to complete assembly tasks for our client based in Melbourn, near Royston. Ideally you will have access to your own transport due to the shift pattern requirements. Responsibilities: Assembling small plastic components Requirements: Experience assembling small items Attention to detail, good dexterity and an awareness of quality requirements Cleanroom experience would be useful but full training will be given. You must be comfortable in lab PPE including hairnet, shoe covers, gloves and coat Familiarity with a glovebox assembly would be beneficial Please contact us as soon as possible for more details or apply below!
Jun 01, 2026
Seasonal
Location: Melbourn, near Royston (SG8) Type of Work: Temporary Duration: 3 months initially, option to transfer to permanent staff for the right candidates Hours: 8am - 4.30pm, Monday to Friday (37.5 hour week) Will move to early / late shift in due course (6am - 2:30pm and 1:30pm - 10pm on a weekly rotation) Salary: £17 per hour Job Reference: 36151 Polytec are looking for Cleanroom Technicians to complete assembly tasks for our client based in Melbourn, near Royston. Ideally you will have access to your own transport due to the shift pattern requirements. Responsibilities: Assembling small plastic components Requirements: Experience assembling small items Attention to detail, good dexterity and an awareness of quality requirements Cleanroom experience would be useful but full training will be given. You must be comfortable in lab PPE including hairnet, shoe covers, gloves and coat Familiarity with a glovebox assembly would be beneficial Please contact us as soon as possible for more details or apply below!
Manufacturing Technician Location: Office based, Whiteley PO15 7AF Salary: £29,000-£33,000, depending on skills and experience Contract: Full Time, Permanent What we offer: In common with many start-ups, we offer a fast-paced, dynamic environment where you can learn a huge amount in a short time, with exposure to everything happening in the company. We look after our staff as they are our key asset, and offer regular salary reviews, share options, lots of flexibility and generous training allowances. Our facilities are commutable from most of Hampshire, West Sussex, Poole, Bournemouth etc. About the company: iFAST is an innovative new medical technology spinout from the University of Southampton, led by an experienced team of entrepreneurs and scientists. We have developed a game changing microfluidics based test for antimicrobial susceptibility, reducing the test time from 48+ to 3 hours to help combat the global threat of antimicrobial resistance, which kills more than 1 million people per year. Job Role: We are now seeking a manufacturing technician to join our team in Whiteley, Hampshire, reporting to our Head of Manufacturing Operations, to help us build our diagnostic instruments. Responsibilities: Manufacturing & Assembly • Assemble instruments and sub-assemblies in accordance with approved work instructions and SOPs. • Carry out mechanical, electrical and electromechanical builds including basic wiring, fitting, alignment and functional checks. • Perform in-process testing, verification steps and instrument-level checks to ensure build quality. • Maintain accurate, clear and compliant manufacturing records, including batch documentation and traceability logs. • Report and document problems and/or obstacles with Quality, processes, equipment and materials to Manufacturing Engineering. • Keep a clean, organised and controlled work area in line with GMP expectations. Quality System Responsibilities • Work within medical device quality system in accordance with EN ISO 13485:2016 and 21 CFR 820. • Operate and maintain manufacturing equipment in line with relevant SOPs. • Participate in Quality discussions, raising observations, ideas and corrective actions where appropriate. • Support non-conformance investigations by providing technical input, build history and documentation. • Contribute to continuous improvement activities across manufacturing processes and documentation. Support & Collaboration • Provide technical support to Quality (e.g. training, input into non-conformance investigations, customer complaints). • Assist with documentation in accordance with standards, manufacturing procedure documentation, and SOPs. • Provide feedback and support for continuous improvement projects. • Periodically presenting your work to the team and our collaborators, and performing other tasks as assigned. Knowledge, Skills & Experience: Essential • Good numeracy and IT literacy and ability to follow and write detailed written instructions. • Experience work in a regulated manufacturing environment working to ISO 13485 or GMP or GLP. • Strong practical skills with hands on assembly, precision tools and manufacturing equipment. • Ability to work methodically with excellent attention to detail and documentation accuracy. • Strong teamwork skills and the ability to manage and prioritise your own workload. • Good problem-solving ability and confidence to raise issues or suggest improvements. • Ability to read and interpret engineering drawing (e.g. CAD). Desirable • Experience with wiring, cable harnesses, crimping or soldering. • Experience working in a controlled environment such as a cleanroom or GLP laboratory. • Previous experience assembling electromechanical or diagnostics instruments. • Experience of lean manufacturing and/or Six Sigma. If you feel you have the necessary skills and experience to be successful in this role, click on APPLY today, forwarding an up-to-date copy of your CV for consideration in the first instance. No agencies please.
May 29, 2026
Full time
Manufacturing Technician Location: Office based, Whiteley PO15 7AF Salary: £29,000-£33,000, depending on skills and experience Contract: Full Time, Permanent What we offer: In common with many start-ups, we offer a fast-paced, dynamic environment where you can learn a huge amount in a short time, with exposure to everything happening in the company. We look after our staff as they are our key asset, and offer regular salary reviews, share options, lots of flexibility and generous training allowances. Our facilities are commutable from most of Hampshire, West Sussex, Poole, Bournemouth etc. About the company: iFAST is an innovative new medical technology spinout from the University of Southampton, led by an experienced team of entrepreneurs and scientists. We have developed a game changing microfluidics based test for antimicrobial susceptibility, reducing the test time from 48+ to 3 hours to help combat the global threat of antimicrobial resistance, which kills more than 1 million people per year. Job Role: We are now seeking a manufacturing technician to join our team in Whiteley, Hampshire, reporting to our Head of Manufacturing Operations, to help us build our diagnostic instruments. Responsibilities: Manufacturing & Assembly • Assemble instruments and sub-assemblies in accordance with approved work instructions and SOPs. • Carry out mechanical, electrical and electromechanical builds including basic wiring, fitting, alignment and functional checks. • Perform in-process testing, verification steps and instrument-level checks to ensure build quality. • Maintain accurate, clear and compliant manufacturing records, including batch documentation and traceability logs. • Report and document problems and/or obstacles with Quality, processes, equipment and materials to Manufacturing Engineering. • Keep a clean, organised and controlled work area in line with GMP expectations. Quality System Responsibilities • Work within medical device quality system in accordance with EN ISO 13485:2016 and 21 CFR 820. • Operate and maintain manufacturing equipment in line with relevant SOPs. • Participate in Quality discussions, raising observations, ideas and corrective actions where appropriate. • Support non-conformance investigations by providing technical input, build history and documentation. • Contribute to continuous improvement activities across manufacturing processes and documentation. Support & Collaboration • Provide technical support to Quality (e.g. training, input into non-conformance investigations, customer complaints). • Assist with documentation in accordance with standards, manufacturing procedure documentation, and SOPs. • Provide feedback and support for continuous improvement projects. • Periodically presenting your work to the team and our collaborators, and performing other tasks as assigned. Knowledge, Skills & Experience: Essential • Good numeracy and IT literacy and ability to follow and write detailed written instructions. • Experience work in a regulated manufacturing environment working to ISO 13485 or GMP or GLP. • Strong practical skills with hands on assembly, precision tools and manufacturing equipment. • Ability to work methodically with excellent attention to detail and documentation accuracy. • Strong teamwork skills and the ability to manage and prioritise your own workload. • Good problem-solving ability and confidence to raise issues or suggest improvements. • Ability to read and interpret engineering drawing (e.g. CAD). Desirable • Experience with wiring, cable harnesses, crimping or soldering. • Experience working in a controlled environment such as a cleanroom or GLP laboratory. • Previous experience assembling electromechanical or diagnostics instruments. • Experience of lean manufacturing and/or Six Sigma. If you feel you have the necessary skills and experience to be successful in this role, click on APPLY today, forwarding an up-to-date copy of your CV for consideration in the first instance. No agencies please.
Berry Recruitment are NOW hiring for a committed and experienced Nutraceutical Operator to join our client based in Oxford. We are seeking a reliable and detail-focused Manufacturing Technician to join our nutraceutical production team. This is a hands-on role within a structured, GMP-aligned environment, supporting the manufacture of high-quality products including powders, capsules, and tablets. Role: Nutraceutical Operator Location: Oxford, Oxfordshire Hours: Full-time, 08:00 - 16:30 Key Responsibilities: Operate machinery including Pill presses, Capsule fillers and blending equipment Operate production equipment in line with validated manufacturing processes Carry out batch manufacturing activities in accordance with GMP and SOPs Perform production and packaging procedures following approved documentation Complete and maintain accurate batch records to ensure full traceability Clean and sanitise processing equipment and production areas in line with procedures Monitor manufacturing processes and report any deviations, adverse events, or environmental abnormalities Promote and adhere strictly to CGMP standards and Health & Safety regulations Support Right First-Time manufacturing principles Assist across the Production Department as required About You: Experience working in regulated production environments (cleanroom experience desirable) Strong understanding of GMP and compliance procedures High attention to detail and accuracy in documentation Proactive, reliable, and able to work effectively within a team No candidate will meet every single desired qualification listed. If your experience differs slightly but you believe you can bring value to this role, we would still love to hear from you. For more information and to apply, contact the Oxford branch of Berry Recruitment on (phone number removed) or click 'Apply Now' to submit your application. Please note that no terminology in this advert is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and ability to perform the duties of the job.
May 21, 2026
Full time
Berry Recruitment are NOW hiring for a committed and experienced Nutraceutical Operator to join our client based in Oxford. We are seeking a reliable and detail-focused Manufacturing Technician to join our nutraceutical production team. This is a hands-on role within a structured, GMP-aligned environment, supporting the manufacture of high-quality products including powders, capsules, and tablets. Role: Nutraceutical Operator Location: Oxford, Oxfordshire Hours: Full-time, 08:00 - 16:30 Key Responsibilities: Operate machinery including Pill presses, Capsule fillers and blending equipment Operate production equipment in line with validated manufacturing processes Carry out batch manufacturing activities in accordance with GMP and SOPs Perform production and packaging procedures following approved documentation Complete and maintain accurate batch records to ensure full traceability Clean and sanitise processing equipment and production areas in line with procedures Monitor manufacturing processes and report any deviations, adverse events, or environmental abnormalities Promote and adhere strictly to CGMP standards and Health & Safety regulations Support Right First-Time manufacturing principles Assist across the Production Department as required About You: Experience working in regulated production environments (cleanroom experience desirable) Strong understanding of GMP and compliance procedures High attention to detail and accuracy in documentation Proactive, reliable, and able to work effectively within a team No candidate will meet every single desired qualification listed. If your experience differs slightly but you believe you can bring value to this role, we would still love to hear from you. For more information and to apply, contact the Oxford branch of Berry Recruitment on (phone number removed) or click 'Apply Now' to submit your application. Please note that no terminology in this advert is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and ability to perform the duties of the job.
