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• QC Senior Equipment Technical Specialist (Temp), • Hertfordshire, UK – On Site / 100%, • 1-year contract – PAYE This role is responsible for supporting all Quality Control (QC) laboratory equipment and associated electronic systems throughout their full lifecycle. The position supports technical developments within the QC laboratory environment and oversees third‑party contractors to ensure operations are conducted in line with internal procedures, current Good Manufacturing Practice (cGMP), and applicable regulatory expectations. The role ensures that QC laboratory systems and software used to support the manufacture, testing, packaging, storage, and distribution of marketed drug products remain compliant with GMP, data integrity, and corporate quality requirements. Key Responsibilities • Support and deliver qualification and validation of QC equipment, processes, and electronic systems in line with internal procedures, GMP, and GAMP guidelines., • Provide input into the drafting, review, and approval of quality policies, systems, and procedures related to QC equipment and systems., • Ensure QC laboratory systems and software remain in a qualified and compliant state., • Act as a strong advocate for data integrity principles across all systems and equipment., • Support procurement of new laboratory equipment and software, including forecasting for replacements and upgrades., • Coordinate and lead equipment servicing, calibration, repair, and maintenance activities., • Manage relationships with external vendors and service providers, including technical support and helpdesk services., • Coordinate vendor site visits, raise purchase orders, and ensure accurate traceability of equipment documentation (e.g. service reports, calibration certificates)., • Support ongoing operation, maintenance, and improvement of manual and electronic systems., • Coordinate with internal IT teams to ensure systems align with corporate IT and quality policies., • Manage system updates and upgrades, ensuring continued qualification., • Ensure procedures are in place and followed for data backup, archiving, retrieval, and access management., • Lead and manage QC equipment and software projects internally., • Support and raise change controls to ensure qualification and validation requirements are addressed., • Maintain equipment and project trackers to ensure visibility, scheduling, and compliance., • Support review and approval of commercial off‑the‑shelf (COTS) documentation., • Provide technical support and troubleshooting for QC analysts and system users., • Prepare and update SOPs and training materials related to equipment and systems. Support investigations related to equipment issues, deviations, CAPAs, and incidents., • Complete maintenance and work orders in a timely manner., • Communicate equipment‑related updates clearly to all stakeholders., • Ensure all activities are performed in line with GMP, GDP, internal quality systems, and industry standards., • Maintain a safe working environment and report incidents and near‑misses in line with procedures., • Ensure product quality through adherence to approved processes and documentation., • Identify opportunities for continuous improvement, efficiency, and innovation., • Maintain strong communication with internal stakeholders and external partners., • Perform duties in line with role objectives, behaviours, and competencies. Skills & Qualifications • Strong knowledge of QC laboratory equipment qualification and validation., • Working knowledge of computerized system validation (CSV) and GAMP., • Good understanding of GMP, data integrity, and regulatory requirements., • Experience with analytical software, electronic QC systems, and quality systems., • Ability to analyse user requirements and drive system improvements., • Strong communication skills with the ability to translate technical concepts clearly., • Sound technical and scientific judgement., • Proficiency with standard office software (Word, Excel, PowerPoint)., • Strong experience with QC laboratory equipment qualification and validation., • Working knowledge of CSV, GAMP, GMP, and data integrity requirements., • Experience supporting analytical software and electronic QC systems. For more information, please contact This role does not offer sponsorship, and you must be happy to work 100% on site in Hatfield. No relocation.

• Quality Control Analyst (temp role), • Hertfordshire, UK – 100% on site, • 1-year contract, temporary role, • Hourly rate – PAYE Cpl Life Sciences is collaborating with a global, research‑led pharmaceutical company focused on developing high‑quality medicines, with a strong emphasis on science, quality, and improving patient outcomes worldwide. This role is responsible for ensuring all materials are tested in line with approved specifications, procedures, and timelines, supporting the timely release and distribution of pharmaceutical products in compliance with GMP and quality standards. Key Responsibilities • Perform QC testing of materials in line with approved specifications., • Qualify, maintain, and calibrate laboratory equipment (URS, IQ, OQ, PQ)., • Maintain laboratory quality systems and documentation., • Support audits, inspections, deviations, CAPAs, and change controls., • Support stability programmes, tech transfer activities, and data reporting (e.g. PQRs, KPIs)., • Collaborate cross‑functionally with Quality, Manufacturing, Supply Chain, and Regulatory teams. Skills & Experience • Strong knowledge of QC, GMP, and pharmaceutical manufacturing/packaging., • Ability to interpret data and apply sound scientific judgement., • Comfortable working cross‑functionally in a regulated environment., • Good communication, organisation, and time‑management skills. For more information, please contact me at This role does NOT offer job sponsorship, and you must be close to the site and be able to work 100% on site.

Talentmark are recruiting for an experienced Maintenance and Asset Coordinator to join a well-established and successful global pharmaceutical company, based in Hatfield, Hertfordshire, on a permanent basis. This is an onsite based role, working 7:30am - 4pm Monday - Friday. Key duties will include: • To ensure the effective operation and continuous improvement of the Computerised Maintenance Management System (CMMS), supporting the planning, coordination, and execution of maintenance and facilities activities., • To act as a central interface between engineering and operational teams, enabling data-driven decision-making, optimising asset performance, and supporting regulatory compliance., • To proactively plan and collaborate with stakeholders to ensure maintenance activities are delivered and closed out on time, in full compliance with GMP standards. Your Background: • Proven experience working with CMMS platforms (e.g., Maximo, SAP, Hexagon, Concept), • Experience in coordinating with cross-functional teams including engineering, operations, and quality assurance, • Ability to produce and interpret maintenance performance reports and KPIs, • Strong understanding of GMP (Good Manufacturing Practice) and Home Office compliance requirements would be an advantage Apply:It is essential that applicants hold entitlement to work in the UK. Please quote job reference 184991 in all correspondence.

Our client a leading research based pharmaceutical organisation with an extensive portfolio across the Oncology, Neurology and Pain therapy areas. By joining our client, you will be working for an organisation with a human healthcare philosophy, which means that we put the patient first in everything we do. As the maintenance and asset coordinator you will ensure the effective operation and continuous improvement of the Computerised Maintenance Management System (CMMS), supporting the planning, coordination, and execution of maintenance and facilities activities across the pharmaceutical site. A key aspect of the role is proactive planning and collaboration with stakeholders to ensure maintenance activities are delivered and closed out on time, in full compliance with GMP standards, site procedures, and Home Office requirements. This role acts as a central interface between engineering and operational teams, enabling data-driven decision-making, optimising asset performance, and supporting regulatory compliance through accurate system management and reporting. What are we looking for? Essential: • Proven experience working with CMMS platforms (e.g., Maximo, SAP, Hexagon, Concept) in a regulated environment., • Experience in coordinating with cross-functional teams including engineering, operations, and quality assurance., • Familiarity with preventive and corrective maintenance strategies, asset lifecycle management, and work order close-out processes., • Ability to produce and interpret maintenance performance reports and KPIs., • Experience supporting audit readiness through accurate documentation and system records., • Proficiency in Microsoft Office tools, especially Excel, for reporting and data analysis. Desirable: • Demonstrable experience in maintenance planning and scheduling within a regulated or GMP-compliant environment., • Strong understanding of GMP (Good Manufacturing Practice) and Home Office compliance requirements related to maintenance and facilities., • Experience working in a pharmaceutical or life sciences environment., • Knowledge of validation and qualification processes related to equipment and facilities., • Familiarity with change control, deviation, and CAPA processes in a GMP setting., • Experience with continuous improvement initiatives., • Exposure to engineering project coordination or shutdown planning., • Understanding of asset reliability and performance monitoring tools or techniques., • Experience in training CMMS users and supporting system upgrades or implementations., • Working knowledge of EHS (Environment, Health & Safety) requirements related to maintenance activities. What our client offers in return • A competitive salary and excellent wider benefits package that includes,, • Electric charging points for Electric/Hybrid vehicles, • Discretionary Bonus, • Free onsite parking, • Subsidised onsite restaurant and coffee shop, • Learning and development opportunities, • Retail discounts, • Well-being & mental health awareness programmes, • Multi-faith prayer room, • You will also be based out of our excellent EMEA Knowledge Centre (EKC) facility, which is our EU Headquarters, and offers an inclusive, and collaborative working environment.

Our client is a leading research based pharmaceutical organisation with an extensive portfolio across the Oncology, Neurology and Pain therapy areas. Our client make tablets, packages these into blisters, label and package vials and bottles. We also manage the wider medicines supply chain and other companies who undertake work on our behalf. By joining our client, you will be working for an organisation with a human healthcare philosophy, which means that we put the patient first in everything we do. Your new role To provide project and operational support in order to maintain a compliant operation within the manufacturing / packaging facilities of the companies European Knowledge Centre (EKC), Hatfield. To ensure that operations conducted are performed in accordance with the requirements of Corporate Standards, Quality System, GMP and GDP Guidelines and industry standards. Duties are performed to ensure: • A safe working environment is maintained for self and other employees, ensuring all near miss incidents and accidents are reported in accordance with procedures., • The Quality of products manufactured and released is assured through adherence to all procedures., • Opportunities to improve operations and reduce cost are identified and progressed through the continuous improvement and demand innovation initiatives., • Companies philosophy of hhc is at the forefront of daily activities., • All stakeholder and customer expectations are understood and met through communication., • Performance is in line with personal and company objectives with demonstrated behaviours and competencies. What are we looking for? • Time served apprenticeship including City & Guilds &/or NVQ 3 - 4 qualifications within an appropriate engineering, building services or construction related discipline., • Demonstrated experience managing building services projects within the pharmaceutical industry preferred but not essential., • Working knowledge of CDM Regulations and EHS qualifications desirable., • Formal project management training / qualifications preferred but not essential., • A growth mind-set with a focus on continued self-development., • Good leadership and interpersonal skills., • Developed problem solving and decision making capabilities., • Ability to work independently or part of a multi-disciplined team., • Adaptable and flexible to cope with the changing priorities of production operations., • Resilient and determined providing robust engineering solutions within an agile environment., • Developed oral and written communication skills., • Developed attention to detail and with an aptitude for neat, clear documentation.

The Senior Engineering Technician is a hand’s on, role reporting to the Senior Production Engineering Manager. As Senior Engineering Technician you shall be responsible for coordination with Production Operations and efficient day-to-day planning of Engineering works. They will lead and direct the Production Engineering Technicians on their respective shifts. As Senior Engineering Technician you shall also be responsible for coaching and mentoring the Emerging Talent cohort (Engineering Apprentices and trainees) to be capable of meeting future engineering needs. In addition, this role is responsible for the reliable and GMP compliant operation of the Production related equipment on Manufacturing and Packaging machinery and supporting systems within the EKC facility at Hatfield. “To ensure that operations carried out within your area of responsibility are carried out in accordance with the requirements of the company Quality System, GMP Guidelines and Industry Standards.” Core responsibilities • Efficient allocation of Engineering resources to meet daily operational requirements., • Planning and coordinating of Engineering maintenance activities., • Mentoring and development of the Emerging Talent cohort., • Setting and maintaining high standards and behaviours. Requirements of role • Maintenance, fault finding and repair of all pharmaceutical equipment and controls associated with Oral Solid Dose Production processing and Packaging equipment, such that production priorities are met, and the equipment performs to its optimum capability and maintains GMP compliance., • Project involvement working with other departments, • Equipment failure reports on CMMS systems. e.g Maximo, • Corrective and Preventative actions and to prevent re-occurrence of faults., • Multi-disciplined, flexible attitude to team working., • Application of Good Manufacturing and Engineering Practices in all areas of responsibility, • Develop, follow, review and update procedures, job plans, certificates and standards., • Setting maintenance regimes for equipment, implementing preventative, run time and reactive maintenance strategies, • Supervision of external contractors and equipment Vendors, • Modification to plant, manufacturing equipment and services., • Co-ordination and participation in the development of risk assessment and method statements associated with specified work., • Deviation investigations to define Corrective and Preventative actions and prevent re-occurrence., • To fully understand and comply with all relevant Site SOP’s, cGMP and safety standards. Preferred Qualifications • Time served apprenticeship and/or relevant engineering qualifications (such as):, • City & Guilds level 3 / Btec Level 3 / ONC/HNC/HND or relevant technical equivalent., • Demonstrated technical experience in engineering, ideally in a pharmaceutical environment in a senior role., • Ability to coordinate, • Fault finding skills, • Ability to read engineering drawings. eg P&ID and loop drawings, • Aptitude for neat, clear and concise documentation., • Good communication and interpersonal skills, • Ability to prioritise and plan own work., • Computer literacy, • Multi-disciplined., • Adaptable and flexible to cope with the changing needs of the production., • A determination to understand breakdown/failure root cause and prevent reoccurrence

• QC Senior Equipment Technical Specialist - MAT Cover, • Hertfordshire, UK – On Site / 100%, • 1-year contract, maternity cover, • Competitive salary This role is responsible for supporting all Quality Control (QC) laboratory equipment and associated electronic systems throughout their full lifecycle. The position supports technical developments within the QC laboratory environment and oversees third‑party contractors to ensure operations are conducted in line with internal procedures, current Good Manufacturing Practice (cGMP), and applicable regulatory expectations. The role ensures that QC laboratory systems and software used to support the manufacture, testing, packaging, storage, and distribution of marketed drug products remain compliant with GMP, data integrity, and corporate quality requirements. Key Responsibilities • Support and deliver qualification and validation of QC equipment, processes, and electronic systems in line with internal procedures, GMP, and GAMP guidelines., • Provide input into the drafting, review, and approval of quality policies, systems, and procedures related to QC equipment and systems., • Ensure QC laboratory systems and software remain in a qualified and compliant state., • Act as a strong advocate for data integrity principles across all systems and equipment., • Support procurement of new laboratory equipment and software, including forecasting for replacements and upgrades., • Coordinate and lead equipment servicing, calibration, repair, and maintenance activities., • Manage relationships with external vendors and service providers, including technical support and helpdesk services., • Coordinate vendor site visits, raise purchase orders, and ensure accurate traceability of equipment documentation (e.g. service reports, calibration certificates)., • Support ongoing operation, maintenance, and improvement of manual and electronic systems., • Coordinate with internal IT teams to ensure systems align with corporate IT and quality policies., • Manage system updates and upgrades, ensuring continued qualification., • Ensure procedures are in place and followed for data backup, archiving, retrieval, and access management., • Lead and manage QC equipment and software projects internally., • Support and raise change controls to ensure qualification and validation requirements are addressed., • Maintain equipment and project trackers to ensure visibility, scheduling, and compliance., • Support review and approval of commercial off‑the‑shelf (COTS) documentation., • Provide technical support and troubleshooting for QC analysts and system users., • Prepare and update SOPs and training materials related to equipment and systems. Support investigations related to equipment issues, deviations, CAPAs, and incidents., • Complete maintenance and work orders in a timely manner., • Communicate equipment‑related updates clearly to all stakeholders., • Ensure all activities are performed in line with GMP, GDP, internal quality systems, and industry standards., • Maintain a safe working environment and report incidents and near‑misses in line with procedures., • Ensure product quality through adherence to approved processes and documentation., • Identify opportunities for continuous improvement, efficiency, and innovation., • Maintain strong communication with internal stakeholders and external partners., • Perform duties in line with role objectives, behaviours, and competencies. Skills & Qualifications • Strong knowledge of QC laboratory equipment qualification and validation., • Working knowledge of computerized system validation (CSV) and GAMP., • Good understanding of GMP, data integrity, and regulatory requirements., • Experience with analytical software, electronic QC systems, and quality systems., • Ability to analyse user requirements and drive system improvements., • Strong communication skills with the ability to translate technical concepts clearly., • Sound technical and scientific judgement., • Proficiency with standard office software (Word, Excel, PowerPoint)., • Strong experience with QC laboratory equipment qualification and validation., • Working knowledge of CSV, GAMP, GMP, and data integrity requirements., • Experience supporting analytical software and electronic QC systems. For more information, please contact This role does not offer sponsorship, and you must be happy to work 100% on site in Hatfield. No relocation.

Job Title – Manufacturing Supervisor. Job Role of the Manufacturing Supervisor. A fantastic opportunity has arisen for an experienced Manufacturing Supervisor to join a well-established UK pharmaceutical manufacturer operating from a modern, state-of-the-art GMP facility in Hertfordshire.

QC Systems & Equipment Specialist Quality Control | GMP Environment | Life Sciences We are currently seeking a QC Systems & Equipment Specialist to support Quality Control laboratory equipment and associated electronic systems across their full lifecycle within a regulated GMP environment. This ro

The Senior Engineering Technician is a hand’s on, role reporting to the Senior Production Engineering Manager. As Senior Engineering Technician you shall be responsible for coordination with Production Operations and efficient day-to-day planning of Engineering works. They will lead and direct the Production Engineering Technicians on their respective shifts. As Senior Engineering Technician you shall also be responsible for coaching and mentoring the Emerging Talent cohort (Engineering Apprentices and trainees) to be capable of meeting future engineering needs. In addition, this role is responsible for the reliable and GMP compliant operation of the Production related equipment on Manufacturing and Packaging machinery and supporting systems within the EKC facility at Hatfield. “To ensure that operations carried out within your area of responsibility are carried out in accordance with the requirements of the company Quality System, GMP Guidelines and Industry Standards.” Core responsibilities - Efficient allocation of Engineering resources to meet daily operational requirements. - Planning and coordinating of Engineering maintenance activities. - Mentoring and development of the Emerging Talent cohort. - Setting and maintaining high standards and behaviours. Requirements of role - Maintenance, fault finding and repair of all pharmaceutical equipment and controls associated with Oral Solid Dose Production processing and Packaging equipment, such that production priorities are met, and the equipment performs to its optimum capability and maintains GMP compliance. - Project involvement working with other departments - Equipment failure reports on CMMS systems. e.g Maximo - Corrective and Preventative actions and to prevent re-occurrence of faults. - Multi-disciplined, flexible attitude to team working. - Application of Good Manufacturing and Engineering Practices in all areas of responsibility - Develop, follow, review and update procedures, job plans, certificates and standards. - Setting maintenance regimes for equipment, implementing preventative, run time and reactive maintenance strategies - Supervision of external contractors and equipment Vendors - Modification to plant, manufacturing equipment and services. - Co-ordination and participation in the development of risk assessment and method statements associated with specified work. - Deviation investigations to define Corrective and Preventative actions and prevent re-occurrence. - To fully understand and comply with all relevant Site SOP’s, cGMP and safety standards. Preferred Qualifications - Time served apprenticeship and/or relevant engineering qualifications (such as): - City & Guilds level 3 / Btec Level 3 / ONC/HNC/HND or relevant technical equivalent. - Demonstrated technical experience in engineering, ideally in a pharmaceutical environment in a senior role. - Ability to coordinate - Fault finding skills - Ability to read engineering drawings. eg P&ID and loop drawings - Aptitude for neat, clear and concise documentation. - Good communication and interpersonal skills - Ability to prioritise and plan own work. - Computer literacy - Multi-disciplined. - Adaptable and flexible to cope with the changing needs of the production. - A determination to understand breakdown/failure root cause and prevent reoccurrence

A proven track record of leading teams within pharmaceutical quality - Strong experience operating as an RP (and ideally RPi) - essential - Deep knowledge of GDP, GMP and MHRA requirements - Someone who communicates clearly and can collaborate and influence stakeholders across the business - A proac

Key Responsibilities Quality, Safety & Compliance - Perform all activities in compliance with GMP, GDP, internal quality systems, and industry standards - Maintain a safe working environment, reporting near misses and incidents in line with procedures - Ensure product quality through strict adhere

A leading pharmaceutical organization in Hatfield seeks a Senior Engineering Technician to oversee production operations.

Eisai EMEA in Hatfield is seeking a Senior Engineering Technician to coordinate engineering tasks and oversee technicians. Candidates should have relevant engineering qualifications and experience in a pharmaceutical setting.

Keywords: quality, QA, compliance, GMP, manufacturing, sterile, aseptic, senior, head, director, manager, team leader, QP, Qualified Person, terminal, sterilisation. We are partnering exclusively with a rapidly expanding advanced pharmaceutical organisation to appoint a senior leader responsible for

Talentmark is recruiting an experienced Maintenance and Asset Coordinator for a global pharmaceutical company in Hatfield, Hertfordshire. The ideal candidate has proven experience with CMMS platforms, can coordinate with cross-functional teams, and possesses a strong understanding of maintenance per

A leading pharmaceutical company in Hatfield is seeking a Senior Engineering Technician to coordinate engineering works and mentor apprentices.The role requires extensive experience in pharmaceutical equipment maintenance, fault finding, and adherence to GMP standards.Responsibilities include planni

Talentmark are recruiting for a QC Analyst, for a a 12 month contractor position, to join a well-established and successful global pharmaceutical company, based in Hatfield, Hertfordshire. Role: This job is responsible for ensuring that all materials are tested according to agreed specifications and procedures and within agreed lead times. Key duties will include : To test all materials according to agreed specifications and procedures. To maintain and calibrate all laboratory equipment. To maintain all laboratory Quality Systems, raise and support the investigation of deviations and support data collection for reporting Quality Assurance Performance Indicators. To write, under supervision, all SOPs associated with QC support. To support the preparation and hosting of competent authority inspections, including preparation for internal and external audits.Your Background: At least 2 years experience in a pharmaceutical Laboratory. Extensive knowledge of Quality Control and Quality Assurance systems. Ability to interpret complex data and present key findings. Demonstrated Knowledge, understanding and application of GMP Guidelines and Regulations.Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence

MANUFACTURING SUPERVISOR Job Title – Manufacturing Supervisor Location – St Albans, Hertfordshire Salary – £42,000 – £45,000 Shift – Monday to Friday (8am – 4pm) Job Role of the Manufacturing Supervisor. A fantastic opportunity has arisen for an experienced Manufacturing Supervisor to join a well-established UK pharmaceutical manufacturer operating from a modern, state-of-the-art GMP facility in Hertfordshire. Following continued growth and internal movement, the company is looking to strengthen its manufacturing leadership team with a motivated and hands-on supervisor. In this role, you will report directly to the Manufacturing Manager and lead a manufacturing team of approximately 15 operators. You will be responsible for overseeing daily production activities while ensuring high standards of quality, compliance, safety, and operational efficiency. The successful candidate will also deputise for the Manufacturing Manager when required. You will coordinate day-to-day manufacturing operations including blending, granulation, compression, and encapsulation processes, ensuring all activities are completed in line with cGMP, SOPs, MHRA requirements, approved batch records, and site safety procedures. The position also involves monitoring production performance, managing workflow, and supporting continuous improvement initiatives across the manufacturing department. Sector – Pharmaceutical Manufacturing Non-Negotiable Requirements of the Manufacturing Supervisor Supervisory or leadership experience within a pharmaceutical or GMP-regulated manufacturing environment. Requirements for the Manufacturing Supervisor. Experience leading and developing production teams within a regulated manufacturing environment. Strong understanding of cGMP standards, SOPs, and MHRA requirements. Experience managing deviations, investigations, and CAPA processes. Confident communication, leadership, and team management skills. Desirable Requirements for the Manufacturing Supervisor. Engineering or pharmaceutical qualification (Level 3 or equivalent). Experience supporting audits and cross-functional collaboration with QA, QC, Engineering, and Production Planning teams. The Manufacturing Supervisor will benefit from: Working for a stable and well-established pharmaceutical manufacturer. Competitive salary package of £42,000 – £45,000 depending on experience. Monday to Friday working hours (8am – 4pm) supporting work-life balance. 28 days holiday (inclusive), pension scheme, and bonus opportunities. Long-term career progression within a growing GMP manufacturing environment. If you are interested in this role and feel that you have the right skills, then please click apply at the bottom of this advert. For further details contact Consultant Name at Pioneer Selection. As a registered candidate with Pioneer Selection Ltd, you automatically become eligible for our referral scheme. You will receive £250 for every candidate we place in permanent employment who has been recommended by you. Terms and Conditions apply – please see our website for further details

Talentmark are recruiting for a QC Senior Equipment Technical Specialist, to join a long-established global pharma company, based in Hatfield on a 12-month temporary basis. The Role: The Senior Technical Specialist will be responsible for supporting all QC equipment and electronic systems through the equipment’s life cycle used within the Quality Control Laboratory. This includes supporting all technical developments within EML’s laboratory as well as third party contracting activities to ensure operation in accordance with the requirements of the departmental Standard Operating Procedures and cGMP. Responsibilities: Ensure Quality Control Laboratory systems and software used to support the manufacture, packaging, testing, storage and distribution of marketed drug products comply with current GMP and Eisai Corporate expectations. Lead the Qualification and Validation of EML QC equipment, processes and systems to ensure performance in line with EML procedures, GMP and GAMP guidelines for process, equipment and electronic systems. Support the procurement of new equipment and providing forecast for new/replacement lab equipment/software. Lead the maintenance of EML procedures supporting Qualification and Validation ensuring they are current with updated requirements for Qualification and Validation and cGMP, cGxP expectations. Lead and complete method transfer projects with third party approved contract laboratories as required. Support QC team members with training and education on use of specialist QC equipment as required. Ensure user access to systems is maintained in line with procedures and support is provided to facilitate the set up and change management of system data to ensure continuous system availability and functionality.Your Skills: Strong knowledge of pharmaceutical Quality Control equipment and electronic system qualification, validation and method transfers. Excellent communication and good people management skills to support progression of technically led projects internally and externally. Ability to understand and analyse user requirements to facilitate changes and system improvements. Working knowledge of electronic systems, CSV and GAMP requirements. Good understanding of the requirements of data integrity and application to system management. Working knowledge of Quality Control Systems and analytical software and electronic Quality Systems. Thorough understanding of GMP Guidelines and Regulations.Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence

QA OFFICER Job Title – QA Officer Location – St Albans, Hertfordshire Salary – £28,000 - £32,000 Shift – Monday to Friday (8am – 4pm) Job Role of the QA Officer A fantastic opportunity has arisen for a QA Officer to join a well-established and growing pharmaceutical manufacturing business. This is an excellent role for someone looking to develop their career within Quality Assurance, working in a modern, state-of-the-art facility with strong investment and long-term stability. The QA Officer will play a key role in ensuring the Quality Management System (QMS) is robust, compliant, and continuously improved, supporting all aspects of manufacturing, documentation, supplier quality, and regulatory compliance. You will be responsible for maintaining high quality and compliance standards across the business, ensuring all products meet regulatory and GMP requirements. Sector – Pharmaceutical Manufacturing Non-Negotiable Requirements of the QA Officer Previous QA experience Experience working within a pharmaceutical or regulated environment Requirements for the QA Officer Worked in a quality assurance role Pharmaceutical experience Desirable Requirements for the QA Officer Pharmaceutical manufacturing background Experience supporting regulatory submissions Knowledge of batch record review and product quality reviews Experience working with Quality Management Systems (QMS) Strong understanding of GMP and regulatory standards (MHRA, ISO) Experience with documentation control and SOP writing Ability to manage deviations, CAPAs, and change controls Strong attention to detail and organisational skills Key Responsibilities Maintain and improve the Quality Management System (QMS) Conduct internal audits and ensure CAPAs are completed Manage controlled documents, SOPs, and batch records Review batch records to ensure compliance with licences Support regulatory submissions and external audits Manage deviations, investigations, and risk assessments Oversee supplier quality and maintain quality agreements Track and report quality KPIs, driving continuous improvement The QA Officer will benefit from: Working for a well-established pharmaceutical manufacturer Brand-new, state-of-the-art facility with significant investment Stable Monday–Friday working hours Opportunities for career development and progression Competitive benefits package and holiday allowance If you are interested in this role and feel that you have the right skills, then please click apply at the bottom of this advert. For further details contact Rinku Patel As a registered candidate, you will also be eligible for our referral scheme. You will receive £250 for every candidate we place in permanent employment who has been recommended by you. Terms and Conditions apply

Talentmark are recruiting for a QC Equipment Technical Specialist, to join a long-established global pharma company, based in Hertfordshire on a 12-month Fixed Term Contract. The Role: The Equipment Technical Specialist will be responsible for supporting all QC equipment and associated electronic systems through the equipment’s life cycle used within the Quality Control Laboratory. This includes supporting all technical developments within manufacturing laboratory as well as third party contracting activities to ensure operation in accordance with the requirements of the departmental Standard Operating Procedures and cGMP. Responsibilities: Ensure Quality Control Laboratory systems and software used to support the manufacture, packaging, testing, storage and distribution of marketed drug products comply with current GMP and Eisai Corporate expectations. Support and deliver the required qualification and validation of lab QC equipment, processes and systems to ensure performance in line with lab procedures, GMP and GAMP guidelines for process, equipment and electronic systems. Support the procurement of new equipment and providing forecast for new/replacement lab equipment/software. Lead the maintenance of lab procedures supporting Qualification and Validation ensuring they are current with updated requirements for Qualification and Validation and cGMP, cGxP expectations. Coordinate and lead equipment service and repair activities. Support QC team members with training and education on use of specialist QC equipment as required. Ensure user access to systems is maintained in line with procedures and support is provided to facilitate the set up and change management of system data to ensure continuous system availability and functionality.Your Skills: Strong knowledge of pharmaceutical Quality Control equipment and electronic system qualification, and validation. Ability to understand and analyse user requirements to facilitate changes and system improvements. Working knowledge of electronic systems, CSV and GAMP requirements. Good understanding of the requirements of data integrity and application to system management. Working knowledge of Quality Control Systems and analytical software and electronic Quality Systems. Thorough understanding of GMP Guidelines and Regulations.Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence

Ideal candidates should have experience in radiopharmaceutical or aseptic production, work well in teams, and comply with GMP regulations.

Ideal candidates will have experience in aseptic services and quality assurance, a keen eye for detail, and understand GMP.

A leading NHS trust in London is seeking an enthusiastic Band 5 Radiopharmacy Technician to join their Radiopharmacy team.Candidates should have attention to detail, effective communication skills, and the ability to work under pressure.Experience in aseptic manufacturing and working with radioactiv

Key responsibilities include preparing, compounding, and dispensing aseptic products under GMP standards.

This role leads end-to-end financial operations for a strategic GMP partnership within the global eyewear and vision care category.

Candidates should have GMP experience, attention to detail, and proficiency in documentation.

A global pharmaceutical company in the UK is seeking a Senior Virus Seed Technician to support the production of virus seeds for Foot & Mouth Disease antigen manufacturing.The role includes managing production activities, maintaining compliance with established standards, and coordinating stock move

This role involves technical expertise in GMP rectification and equalisation, as well as engaging in actuarial projects across pension-related initiatives.

A global consulting firm seeks an Actuarial Consultant to drive GMP equalisation and engage in actuarial projects.

CBRE in Stevenage is looking for a Calibration Technician to calibrate and adjust equipment as per customer requirements.The role involves performing calibrations across various disciplines and maintaining precise documentation.Candidates should have a background in instrumentation or similar fields

The ideal candidate will have over 7 years of experience in the Biotech or pharmaceutical sectors, particularly in cGMP environments.

A leading recruitment firm in Greater London is seeking a detail-oriented QC Materials Technician to ensure compliance and quality standards in a GMP-regulated environment. The ideal candidate should have at least 1 year of experience in a GxP or GMP setting, possess strong communication skills, and

The GMP Production Manager will be responsible for establishing the GMP production team and taking a lead role in the operation of the GMP production suites. The GMP Production Manager will lead and develop the GMP production team and will be responsible for leading the day-to-day management, operat

A healthcare agency is seeking an experienced Pharmacist with NHS Hospital experience to join their team in Greater London.The ideal candidate will be GPhC registered, compliant with regulations, and able to work flexible hours, both part-time and full-time.In return, the agency offers excellent pay

Join Our Team as an Actuarial Consultant - GMP Equalisation and Project Work (Nationwide). Are you a talented and ambitious actuary with a strong background in GMP rectification and equalisation? At Mercer, we are excited to expand our dynamic team by welcoming skilled part-qualified or qualified ac

Ideal candidates will have strong knowledge of GMP, HACCP, and tracing in manufacturing environments.

Ideal candidates will have a relevant graduate qualification, knowledge of GMP in a pharmaceutical context, and communication skills to interact at all management levels.

A global ecommerce group is hiring a Machine Operative for their production team in Blackpool, England.In this role, you will ensure safety and quality standards while operating and maintaining high-speed production equipment.Ideal candidates possess strong communication skills, attention to detail,

A leading medical technology company in Cirencester is seeking a Senior Validation Engineer to maintain the validated state of critical medical device manufacturing processes.The role involves leading validation projects, supervising a team, and ensuring compliance with regulatory standards.Candidat

This role involves managing validation compliance activities and ensuring all processes meet GMP and corporate standards.

Greencore Group plc is seeking a Night Shift Quality Auditor for its Spalding site in the United Kingdom.The successful candidate will ensure compliance with quality management systems and food safety standards while supporting continuous improvement initiatives.Key responsibilities include conducti

Ipsen Group in Dublin is looking for a talented Plant Engineer to contribute to the production of Active Pharmaceutical Ingredients (APIs).The ideal candidate will have 5 years' experience in maintenance engineering within the pharmaceutical industry, focusing on HVAC, lyophilization, and process ab

This senior leadership position involves overseeing all engineering and technical operations within a GMP-regulated manufacturing facility.

Responsibilities include ensuring GMP compliance, training junior staff, and maintaining high standards of production.

WISE Campaign is seeking an Engineering Platform Lead to ensure appropriate platforms for GMP clinical trial material manufacture and support technical expertise for internal GMP projects. The ideal candidate will hold a Bachelor's degree in a relevant discipline and have experience in GMP manufactu

Entrust Resource Solutions is seeking a Manufacturing Manager to oversee site-wide management of manufacturing projects in a GMP environment.