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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 (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.

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.

• 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.

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

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.

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 a...

MANUFACTURING SUPERVISOR Job Title – Manufacturing Supervisor Apply below after reading through all the details and supporting information regarding this job opportunity. 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. xrnqpay 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.

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

Robust and proven Quality Assurance background within the pharmaceutical sector. 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 expandin

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

Eisai EMEA in Hatfield is seeking a Senior Engineering Technician to coordinate engineering tasks and oversee technicians.You will play a key role in ensuring the efficient operation of production equipment and guiding apprentices.Candidates should have relevant engineering qualifications and experi

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

The role requires extensive experience in pharmaceutical equipment maintenance, fault finding, and adherence to GMP standards.

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 (phone number removed) in all correspondence

Talentmark are recruiting for a Quality Validation Associate, to join a well-established and successful global pharmaceutical company, based in Hatfield, Hertfordshire, for a 12 month fixed term contract. Role: You will be responsible for providing Quality oversight, validation expertise and strategic support for the successful delivery of expansion projects. You will ensure that all qualification and validation activities associated with new facilities, utilities, warehouse operations, and packaging lines are planned and executed in accordance with company procedures, regulatory expectations, and industry standards. Key duties will be to: Support the development and implementation of qualification and validation strategies for the company facility expansion project, including the new cold‑chain warehouse, packaging lines, facility extensions and utility modifications. Support the generation, review and approval of project validation documentation including Qualification Plan, URS, Design Qualification, Risk Assessments, FAT/SAT protocols, commissioning documentation, IQ/OQ/PQ protocols, validation reports and traceability matrices in line with company procedures and regulatory expectations. Provide Quality oversight to ensure commissioning and qualification activities are executed in compliance with GMP, GDP, Annex 15, GAMP 5 and company requirements. Coordinate with Engineering, Production, QC, Supply Chain and other stakeholders to ensure equipment, systems and facilities are introduced, qualified and handed over in a controlled and compliant manner in accordance with the company's change management procedures. Support and review validation activities for facility and utility systems such as HVAC, compressed air, environmental monitoring systems and temperature‑controlled storage areas. Provide Quality input to project design reviews, equipment selection, process flow development and risk assessments ensuring validation requirements are incorporated from early project stages. Participate in investigations for deviations or non‑conformances arising during commissioning and qualification, ensuring appropriate root cause analysis, corrective actions and preventive actions are defined. Prepare and update SOPs and training materials associated with qualification, validation and project delivery processes as required. Support project teams with regulatory compliance guidance, ensuring project documentation is inspection‑ready and aligned with cGxP expectations. Identify and implement continuous improvement opportunities to enhance qualification and validation processes, project delivery efficiency and compliance. Provide training and coaching to project personnel and internal stakeholders on qualification, validation and Data Integrity requirements. Act as a strong advocate of Data Integrity, ensuring documentation, testing and record management associated with the projects comply with ALCOA++ principles. Perform any appropriate duties at the request of the Quality Validation Manager.Your Background: Educated to degree level or above in a scientific or related field with significant experience in a pharmaceutical industry role focused on Electronic Quality Systems. Proficient knowledge of electronic systems, CSV and GAMP requirements and the ability to understand and analyse user requirements to facilitate changes and system improvements. Working knowledge of facility and utility systems such as HVAC, compressed air, environmental monitoring systems Good understanding of the requirements of data integrity and application to system management. Good understanding of Quality Control Systems and analytical software and electronic Quality Systems. Good understanding of GMP Guidelines and Regulations. Knowledge of the qualification and validation requirements for equipment and electronic systems. Excellent verbal and written communication skills.Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence

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

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

Identify non-compliance trends and systematic risks within the GMP discipline, communicating these findings to line management and functional leads. Maintain up-to-date knowledge of global GMP regulations and industry trends, identifying new requirements to ensure a high level of quality is mainta

The role involves conducting feasibility and formulation studies, preparing GMP batches, and providing laboratory support across New Product Development.

A European manufacturer of hygienic components based in West Yorkshire is seeking a Quality Technician to ensure product quality and compliance with internal standards.The role involves conducting inspections, managing quality concerns, and supporting continuous improvements.Candidates should have p

Candidates must have a degree in a relevant scientific discipline and prior experience in highly regulated environments such as cGMP or ISO.

The successful candidate will ensure GMP compliance, conduct laboratory experiments, and support project initiatives.

A leading digital recruitment agency in the UK is seeking a senior professional with extensive experience in the Google Marketing Platform (GMP). Candidates must have at least 7 years of GMP experience and a strategic mindset to engage with senior clients successfully.

A growing global pharmaceutical manufacturer in the UK is seeking a Microbiology Manager to lead microbiology activities ensuring compliance in a GMP-regulated environment.

A leading digital marketing technology firm in Greater London is seeking a professional to develop and support its Google Marketing Platform clients.The role requires over 5 years of PPC experience and strong communication skills.You will manage client onboarding, provide technical support, and deli

You will oversee maintenance activities, manage technical documentation, and ensure compliance with GMP regulations. The ideal candidate has experience in GMP environments and relevant engineering education.

Integrating new capabilities for prototyping of tech solutions for both Assembly and GMP Clients. Be an evangelist to help our clients be at the top of their game by helping with their technical solutions of the GMP & GCP tools. Experienced throughout the GMP tech stack.

The ideal candidate should have a strong understanding of GMP and HACCP, effective communication skills, and a commitment to continuous improvement.

A healthcare provider in Watford is seeking an Advanced Pharmacist for its Technical/Cancer Services Department.This role is focused on leading clinical pharmacy services for Haematology and Oncology, supervising staff, and ensuring compliance with all regulatory standards.Ideal candidates should ho

A pharmaceutical company in Greater London is seeking a Process Technician to support production operations within a GMP-regulated environment. Candidates should have experience in GMP or manufacturing environments, and strong attention to detail is essential.

Assist with technical operations in the GMP facility, including equipment lifecycle, goods handling, and validation activities. Maintain the equipment qualification tracker (WASP) to ensure GMP compliance. Manage GMP materials and consumables, including ordering, receiving, storing, and disposal, wh

GMP Recruitment Agency Limited are recruiting for this role on behalf of their client and are acting as an Employment Agency.

NHS Blood and Transplant is seeking an Eye Services Technical Officer to support our Eye Bank team in maintaining high-quality services.This role includes preparing samples, maintaining equipment, and ensuring compliance with standards.The position offers a supportive work environment, flexible work

The role involves executing validation protocols and ensuring compliance with GMP standards.

The role involves providing technical support in aseptic services and ensuring compliance with GMP.

The role involves running the packaging line, ensuring compliance with GMP, and maintaining quality standards while packaging pharmaceuticals.

Deze rol vereist minimaal 2 jaar labervaring, een MLO opleiding, en kennis van GMP/GcLP.

MedPharm seeks a dedicated individual to support the Production and Quality Control departments with daily lab maintenance tasks in their GMP facility.

This hands-on role requires experience in a GMP production environment, where you will operate manufacturing equipment and ensure high standards of cleanliness and quality.

A global pharmaceutical leader is seeking a Packaging Operator to join their production team in England.This mid-senior level role involves operating packaging equipment and ensuring compliance with safety and quality standards.Ideal candidates will have experience in pharmaceuticals or similar regu

A leading global CRO is seeking a Director of Analytical Chemistry for their site in Hoddesdon.This strategic leadership role involves managing scientific teams, ensuring compliance with regulatory standards, and driving performance initiatives.The successful candidate will have extensive experience

Candidates should possess a strong understanding of GMP and HACCP, with excellent communication skills.

Business Development Director, Process Development and GMP Manufacturing. Process Development, Scale-Up and GMP Manufacturing. Identify, qualify and develop new business opportunities across process development, scale‑up, technology transfer and GMP manufacturing.

Cpl Life Sciences is looking for a Quality Operations Associate in the United Kingdom to support Quality Systems and Assurance in a pharmaceutical setting.The role includes maintaining the Quality Management System and participating in audits.Candidates should have a bachelor's degree in life scienc

Candidates should possess strong analytical skills, be IT literate, and have experience in GMP laboratories.