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• Job title: R&D Scientist, • Location: Slough, • Contract Length: 18 months, • Working Hours: 37.5 hours/week, • Pay Rate: £17.96/hour Job description · • Adhere to EHS policy, LSO profile and other site guidance, • Recording data in electronic notebook, • Write study plans and execute experiments, • Buffer and medium preparation, filtration and storage, • Perform and develop nonstandard assay and procedure for project work, • CHO cell culture in deep well plate, shake flask, roller bottles, ambr250 vessel, bioreactor up to 5 litres, • Daily monitoring of culture station for cell growth, viability, metabolites and various process parameters, • Work as part of a team, • Completing housekeeping activities to maintain workplace standards., • Recording all data and results in specified forms (electronic and paper) with accuracy and responsibility and keeping accurate records with GMP and Data Integrity principles in mind., • Lab chores as assigned Experience • Degree: BSc or MSc, • Field: Life Science, Biotechnology, Biochemistry, Molecular Biology, • A basic understanding of mammalian cell culture, • Good level of organization, • Understanding of mammalian process development, • Basic understanding of bioreactor operations, • Familiarity with process analytical technology

• Job title: Scientist (QC Product Testing and Stability), • Location: Slough, • Contract Length: 12 months, • Working Hours: 37.5 hours/week, • Pay: 17.96ph About the Role The role is predominantly lab based for the execution analytical testing e.g. HPLC (size exclusion, ion exchange etc.), electrophoresis (e.g. CE SDS, icIEF), spectrophotometry and general characteristic analysis (e.g. visual appearance, pH, Osmolality) for the purpose of assessing the quality and stability of therapeutic proteins. All work is expected to be carried out in a safe and compliant manner in accordance with local EHS policies and cGMP guidelines. In addition, some time will be spent technically reviewing other analysts assays, writing stability study protocols and data summary reports, SOP updates, and assisting with quality records. Key Responsibilities • Performs experimental work independently in accordance with SOPs and study protocols on a variety of sample types, • Performs work in a safe, compliant manner, ensuring training profile is maintained and up to date at all times., • Plans and completes assigned tasks within the required timeframe. Communicates progress and escalates challenges to Line Manager and/or scientific lead as appropriate, • Technically review assays against SOPs, protocols and GMP principles and liaise with operators and study directors to close out technical review of assays., • Interpret data against specifications, critically assess results and identify trends within data, reporting any observations and concerns to QC management, SDs, QC representative in a timely manner., • Writes stability study protocols, reports, testing summaries etc., • Act as a mentor and/or trainer to newer or more junior members of the team and provide help and support to team mates, • Supports improvement projects within the department and encourages best practice and corrects incorrect/bad practice, • Support, as needed, with the timely completion of investigations, deviations, CAPAs and change controls and may independently lead and complete minor investigations e.g. pipette calibration failure, storage equipment temperature excursions, • Actively contributes to QC department general lab housekeeping, ensuring the laboratory is adequately stocked with reagents and consumables as needed. In addition, perform monitoring and maintenance of equipment and may take on system owner responsibilities, • Work collaboratively in a team to ensure business, regulatory and customer needs are met., • Perform other duties as assigned. Education/experience Required: • BSc in relevant scientific discipline or relevant previous experience - Chemistry / Biochemistry, • Experience - GMP, Pharmaceutical, Biological

Senior QA Validation Specialist Location: Windsor, UK Contract: 6‑month Fixed-Term Contract Industry: Pharmaceuticals About the Role We are currently seeking an experienced Senior QA Validation Specialist to join a pharmaceutical site in Windsor on a 6‑month contract. This role will act as the QA lead for the CQV (Commissioning, Qualification & Validation) department, providing quality oversight and ensuring all validation activities are performed in compliance with GMP and regulatory expectations. This is a senior, site-facing position requiring strong validation knowledge, confident stakeholder interaction, and hands-on QA experience within a regulated pharmaceutical environment. Key Responsibilities • Act as the primary QA representative for the CQV function, • Provide QA oversight for commissioning, qualification, and validation activities, • Review and approve validation documentation including VMPs, protocols, reports, risk assessments, and SOPs, • Ensure CQV activities comply with GMP, regulatory requirements, and internal quality systems, • Support deviations, change controls, CAPAs, and quality risk assessments related to validation, • Partner closely with Engineering, CQV, Manufacturing, and QC teams on site, • Support audit and inspection readiness related to validation activities Skills & Experience Required • Significant experience in QA within a pharmaceutical environment, • Strong working knowledge of validation activities (equipment, utilities, facilities, and systems), • Solid understanding of GMP and regulatory expectations, • Ability to work autonomously and confidently in a senior, site-based QA role, • Excellent documentation review and stakeholder management skills What’s on Offer • 6‑month fixed-term contract at a pharmaceutical site in Windsor, • Senior-level responsibility with meaningful impact on CQV activities, • Collaborative, hands-on site environment If you are an experienced QA Validation professional looking for a short-term senior contract role with clear ownership of CQV quality oversight, we would welcome your application.

Job Title: System Specialist – DMS Location - Slough (Hybrid) Contract length - 6 months Pay - £32 PAYE | £42 UMB Overview: We’re looking for a detail-oriented System Specialist to manage and support our Document Management System (DMS) within a GMP pharmaceutical environment. This role will focus on document lifecycle management, system coordination, and supporting a migration to Veeva Vault. Key Responsibilities: • Manage end-to-end document control (SOPs, work instructions, validation docs), • Act as DMS Super User: workflows, permissions, master data, and reporting, • Support DMS cleanup and migration activities, • Monitor periodic reviews and ensure GMP compliance, • Coordinate document translations across global teams, • Provide user support, training, and troubleshooting Requirements: • Degree in Life Sciences or related field, • 3+ years in document control within GMP pharma, • Experience with DMS (D2 or similar systems), • Strong knowledge of GMP (e.g., 21 CFR Part 11, EU Annex 11), • Excellent organisation and communication skills Why apply? Join a collaborative global team and play a key role in improving quality systems and driving digital transformation.

Soft Services Manager – Scientific The Opportunity An exciting opportunity has arisen for a Soft Services Manager to take ownership of cleaning and support services within a highly regulated healthcare environment. This role plays a vital part in ensuring cleanrooms, controlled spaces, and general areas are maintained to the highest possible standards of cleanliness, safety, and compliance. What You’ll Be Responsible For Ensuring Standards • Take full responsibility for cleaning operations within cleanrooms and controlled environments, • Maintain strict compliance with all regulatory and hygiene requirements, ensuring full audit readiness, • Create, review, and implement SOPs relating to cleaning activities, • Monitor environmental standards, including contamination control and particulate levels, • Oversee a range of services including cleaning, waste disposal, pest control, laundry, and hygiene, • Maintain consistently high standards across both clinical and non-clinical settings, • Manage specialist cleaning activities such as terminal cleans and decontamination procedures, • Manage and support cleaning teams and supervisors to deliver excellent service, • Ensure all team members receive appropriate training in infection control, and health & safety, • Ensure all operations align with current health & safety legislation, • Conduct risk assessments and maintain safe working practices, • Perform regular quality checks and internal audits, • Maintain accurate documentation and cleaning records, • Support external inspections and regulatory audits, • Deliver services in line with agreed KPIs and SLAs, • Provide reporting on performance and service delivery, • Demonstrated experience in a Soft Services or Facilities Management role within regulated industries such as healthcare, pharmaceutical, or GMP environments, • Proven leadership and team management capability, • Solid understanding of health & safety requirements, • Experience with audits, compliance processes, and quality systems, • High attention to detail with a commitment to excellence, • Well-organised with strong problem-solving ability, • Comfortable working within strict regulatory frameworks, • A proactive leader who develops and supports others, • Driven to continuously improve standards and performance

A A globally recognised, innovation‑led healthcare organisation has an exciting opportunity for a Head of Regulatory Affairs to lead its UK Regulatory Affairs function. This senior leadership role will set and deliver regulatory strategy across the UK portfolio, ensuring timely licensing, regulatory compliance, and alignment with EMEA and global objectives. You’ll work closely with cross‑functional teams and external health authorities, with strong influence on business outcomes and regulatory policy. Key Responsibilities: • Lead UK Regulatory Affairs strategy and team, • Oversee MHRA submissions and lifecycle management, • Ensure ongoing regulatory and GMP compliance, • Partner with internal stakeholders across medical and commercial functions, • Lead external engagement with the MHRA and industry bodies, • Develop and retain a high‑performing Regulatory Affairs team Key Requirements: • Life Sciences degree (or equivalent experience), • Extensive UK/EU Regulatory Affairs experience, • Strong knowledge of regulatory frameworks and GMP/QMS, • Proven senior leadership and stakeholder influence If you’re looking to shape regulatory strategy and make a meaningful impact in a highly regulated environment, apply today.

• Job title: QA Associate, • Location: Slough, • Contract Length: 6 months, • Working Hours: 37.5 hours/week, • Pay: up to 23.0 DOE About the Role • Working as part of the QA Documentation Control Team., • Proactively issue documents and labels to Manufacturing based on the schedule and defined timelines obtained from customer departments., • Ensure high standard of documentation issuing are adhered to by self and others., • Maintain the archiving system., • Perform Batch Consolidation (auditing) duties with regard to QC Biochemistry and QC Microbiology testing activities for Drug Product (DP) and Drug Substance (DS). Key Responsibilities • Issuing of approved/ effective GMP documents for use in Manufacturing (entering the unique document ID based on the issue list, printing from DMS and signing the issue list) ensuring that Manufacturing deadlines are met., • Printing of labels for use in the Manufacturing process, including finished product labels., • Checking accuracy of issued documentation and labels, • Issuing of effective logbooks as required according to GMP procedures., • Printing and issuing other GMP documentation as required meeting business timelines, • Co-ordinate the consolidation of all the QC testing activities, • Perform an independent check that all the relevant activities have been completed and all release specifications have been met., • Perform Batch Consolidation duties with regard to QC Biochemistry and Microbiology testing activities for Drug Product and Drug Substance., • Liaise with internal customers to ensure receipt of required information and maintain effective interdepartmental communication and collaboration., • Work with the QA Operations team members, Manager and Team Leaders to enable continued improvement to QA quality systems / processes., • To continually identify and implement improvements in safety, GMP compliance and efficiency., • Leading and management of quality records e.g. Deviations, CAPA, Change Controls, Investigations, • Authoring, Reviewing and approving GMP documentation, • Prioritizing workload to ensure deadlines are met., • Acting as a point of contact for general queries relating to issuing., • Maintenance of issuing supplies to ensure that materials are always available to enable on time issuing of documents., • Maintenance the Slough archiving system by checking received boxes adhere to GMP procedures, arranging for box collection and coordinating box retrieval as required., • Maintenance of training profile, ensuring that all required training is completed prior to performing an activity., • Other duties as assigned. Education/experience Required: • Bachelor of Science (or equivalent experience)- Biology or related field, • Previous work experience in QA / GMP experience is useful though not essential, • IT literate (MS Office – Word, Explorer, Excel, Access, Outlook) familiarity with database entries, • Verbal and written communication skills, • Risk based decision making, • PQS experience, • Accurate data entry skills, high attention to detail, • Demonstrated workload prioritization skills, decision making and scheduling skills, • Ability to meet strict deadlines, • Good organizational and planning skills.

My client is seeking a Junior Quality Assurance & Pharmacovigilance Officer to join our Medical team. This is an excellent opportunity for a life sciences or healthcare graduate to gain hands-on experience in Quality Assurance (QA) and Pharmacovigilance (PV) within a highly regulated environment. Key Responsibilities • Support the maintenance of the Pharmaceutical Quality System and ensure ongoing compliance, • Assist with QA activities, including documentation preparation for audits and internal meetings, • Ensure alignment with local and European regulatory requirements (GDP, GMP, GVP), • Manage training records and update compliance systems (e.g. ComplianceWire), • Review and assess safety information to identify reportable cases and special situations, • Perform accurate and timely data entry into global safety databases, • Follow up on missing or incomplete safety information, • Support the development and maintenance of SOPs and work instructions, • Assist in documenting deviations, CAPAs, and data corrections, • Maintain inspection-ready records with full traceability and audit awareness Key Accountabilities • Ensure accurate, complete, and timely processing of safety cases in line with regulatory timelines, • Maintain high standards of data quality, consistency, and medical relevance, • Support internal audits and provide required documentation, • Ensure appropriate and well-documented follow-up activities, • Maintain compliance with internal procedures and regulatory expectations Key Skills • Degree in Pharmacy, Life Sciences, or a recognised healthcare discipline, • Basic understanding of QA systems and pharmacovigilance requirements (GDP, GMP, GVP), • Strong attention to detail and organisational skills, • Ability to work in a structured, process-driven environment, • Interest in regulatory compliance and patient safety, • Flexible, proactive, and eager to learn

QA Associate Location: Windsor, UK Contract: 6-month initial Fixed-Term Contract Industry: Pharmaceuticals About the Role We are seeking a QA Associate to join the Quality Assurance team at a pharmaceutical production site based in Windsor. This is a 6‑month initial fixed-term contract, ideal for someone with previous pharmaceutical experience and a good understanding of GMP who is looking to build or strengthen their QA background. Key Responsibilities • Support the QA team with day-to-day quality activities on site, • Assist with GMP documentation, including SOPs, deviations, and quality records, • Support batch record review and release activities, • Participate in investigations, CAPAs, and change control processes as required, • Ensure activities are performed in compliance with GMP, company procedures, and regulatory standards, • Work cross-functionally with Production, QC, and other site teams Skills & Experience Required • Previous experience in a pharmaceutical or regulated life sciences environment, • GMP experience is essential, • Previous experience in a Quality Assurance role, • Strong attention to detail and good documentation skills, • Ability to work effectively in a fast-paced, regulated environment What’s on Offer • 6-month fixed-term contract with the opportunity to gain valuable pharmaceutical QA experience in a reputable company, • Exposure to a regulated, GMP-compliant manufacturing environment, • Supportive team and hands-on learning opportunities If you are a QA professional with GMP experience looking for a contract opportunity within the pharmaceutical industry, we would be pleased to hear from you.

Job Summary We are seeking an experienced Document Controller with a strong background in M&E construction environments. The role will support project delivery across fit-out and laboratory projects by ensuring accurate, timely, and compliant management of all project and procurement documentation. The ideal candidate will have experience working with technical documentation, supplier coordination, and strict regulatory environments typical of laboratory builds. Key Responsibilities Document Control & Management • Establish, maintain, and manage document control systems for project and procurement documentation., • Ensure all documents (drawings, RFIs, submittals, specifications) are correctly logged, tracked, and distributed., • Maintain document registers, revision control, and version tracking in line with company and client standards., • Support project teams with document workflows, approvals, and transmittals., • Ensure all M&E drawings and technical documents are up to date and aligned with site activities., • Ensure all documentation complies with QA/QC procedures and project standards., • Maintain audit trails for all document transactions., • Support ISO compliance and internal/external audits., • Use document management systems (e.g., Aconex, Viewpoint, Asite, or similar)., • Generate reports on document status, overdue items, and procurement tracking., • Continuously improve document control procedures and workflows. Requirements Education & Experience • Minimum 3–5 years’ experience as a Document Controller in M&E construction., • Experienced in using Procore software, • Proven experience supporting procurement processes., • Experience in fit-out and laboratory projects is highly desirable.

Role: Associate Principal QA Specialist (CQV) Location – Slough, UK 6 months contract Role Purpose & Scope Enable site operations performance by managing and supporting GMP issues through QMS processes, site governance and senior QA Leadership. Provide oversight on day-to-day Quality Assurance activities in the areas of Validation / Technical Services in accordance with Lonza Corporate requirements, standards and current regulatory requirements, meeting USFDA, European requirements and others as applicable for a multi-product, GMP biotech contract manufacturing facility. Required Skills & Competencies Work Experience Area -QA Level- Advanced - 5-10 years Key Responsibilities To provide shoulder to shoulder review, approval and support for the management of quality records e.g. Deviations, CAPA, Change Controls, Investigations To provide oversight over day-to-day Quality assurance activities in the areas of Technical Services and Validation in accordance with the client Corporate requirements, standards and current regulatory requirements Utilize knowledge of GMP and quality processes within the functional areas to: Manage and escalate Major and Critical compliance issues through the site QMS processes e.g. deviations and CAPAs To actively identify, suggest and participate in continuous improvement activities Mentor and coach business partners in cGMP practices to maintain and develop a cGMP environment Maintain and promote a state of audit readiness Actively suggest, initiate, participate and contribute to PQS process improvements initiatives and projects Provide QA SME support at departmental Local Quality Councils and project meetings Provide shoulder to shoulder review, approval and QA Technical support to key business partners for the management of quality records e.g. Deviations, CAPA, Change Controls, Investigations Provide coaching and training to other team members Provide QA SME support at departmental Local Quality Councils and project meetings Provide QA project support to complex projects Performs other duties as assigned.

• Job title: System Specialist, • Location: Slough (hybrid), • Contract Length: 6 months, • Working Hours: 37.5 hours/week, • £32 p/h About the Role We are seeking a highly organized and detail-oriented System Specialist to support our pharmaceutical manufacturing operations through effective management of the Document Management System (DMS) in preparation to a migration to Veeva Vault system. This role is critical to ensuring documentation related to GMP manufacturing processes is current, compliant, and readily accessible. The System Specialist will support cleanup activities related to the DMS, manage the review and approval workflows of global documents, monitor and report periodic reviews, manage translation activities, and support end users across the organization. Key Responsibilities • Document Lifecycle Management: Manage the end-to-end document control process of global documents in DMS, ensuring timely creation, review, approval, issuance, and archival of controlled documents such as SOPs, work instructions, and validation protocols. • DMS Coordinator Role: Act as Global Super User/Coordinator of DMS application covering: • Management of ownership of documents, • Management of properties for effective documents, • Creation and maintenance of distribution lists, • Management of Secure groups, • Management of review and approval workflows across cross-functional teams including QA, Manufacturing, QC, Engineering, and Regulatory Affairs to ensure alignment and timely approvals., • Maintenance of master data, • User permission management: review, update, grant/remove, • Act as the final approver (gatekeeper) for global documentation during approval workflows, • Support the preparation and distribution of bi-weekly reports on document creation and revisions, • Support all Cleanup activities of the current DMS in preparation for a new eDMS. • Periodic Review Monitoring: Track, monitor and update the Past Overdue Periodic Review Reported, and create monthly reports of periodic document reviews in accordance with GMP and internal procedures. Escalate overdue tasks and non-compliance issues to department leads and Quality leadership. • Translation Coordination: Oversee the translation of controlled documents to support global manufacturing sites. Ensure translated versions become effective simultaneously with the English master to maintain operational consistency. • User Support and Training: Act as the primary point of contact for DMS end users (via QMS Mailbox/F11 tickets), providing system navigation support, troubleshooting, and training to ensure proper use and compliance with established document control procedures, and serve as Local Headquarter (Basel) Training Administrator for Cornerstone. • System Optimization and Compliance: Collaborate with QA and IT teams to enhance document workflows and ensure the document management system is optimized for pharmaceutical manufacturing and compliant with regulatory authority requirements (e.g., FDA, EMA), while supporting the Global QMS-DMS team in implementing system improvements, managing technical issues, and contributing to OQ/PQ testing. Education/experience Required: • Bachelor’s degree in Life Sciences, Quality, or a related technical field (or equivalent experience), • 3+ years of experience in document control within a GMP pharmaceutical manufacturing environment, • Veeva Vault experience highly desired, • Proficiency with DMS (D2) or similar electronic document management systems, • Strong understanding of GMP regulations (21 CFR Part 11, EU Annex 11), and pharmaceutical documentation requirements, • Exceptional attention to detail, organizational, and time-management skills, • Strong interpersonal and communication skills with the ability to work across departments

Associate Principal QA Specialist (CQV) Contract: 6 months Hours: 37.5 hours per week Location: Slough (hybrid – 3 days on site required) Pay: £32.76 per hour PAYE The Role We are currently seeking an experienced Associate Principal QA Specialist (CQV) to support Quality Assurance activities within a GMP pharmaceutical manufacturing environment. This role provides hands‑on QA support to site operations, with a strong focus on Commissioning, Qualification and Validation (CQV) and Technical Services. You will work closely with cross‑functional teams to manage GMP issues through the Quality Management System, maintain audit readiness, and ensure compliance with UK, EU and US regulatory requirements. Key Responsibilities • Provide “shoulder‑to‑shoulder” QA review, approval and support for quality records including deviations, CAPAs, change controls and investigations, • Provide day‑to‑day QA oversight of CQV, Validation and Technical Services activities, • Manage and escalate major and critical GMP compliance issues through QMS processes, • Actively support continuous improvement and PQS process improvement initiatives, • Coach and mentor business partners on cGMP practices to maintain a strong quality culture, • Maintain a constant state of audit readiness, • Act as a QA SME in project meetings, local quality councils and complex site projects, • Support site governance and senior QA leadership activities, • Perform additional QA duties as required Skills & Experience Required • Strong pharmaceutical Quality Assurance background within a GMP environment, • CQV / Validation experience highly desirable, • Solid understanding of GMP, QMS and regulatory expectations (EU & US), • Experience reviewing and approving deviations, CAPAs, change controls and investigations, • Confident communicator with strong stakeholder engagement skills, • Ability to work autonomously while managing priorities and deadlines Qualifications • Science‑based degree (or equivalent experience), • Proven QA experience in pharmaceutical or biotech manufacturing

We are looking for an experienced auditor who can navigate manufacturing environments and work collaboratively with stakeholders to develop corrective actions that ensure long-term systemic stability.

A design-led consultancy delivering high-specification pharmaceutical, biotech and regulated manufacturing facilities is seeking an Electrical Design Lead / Associate Director. Lead electrical design on GMP & pharmaceutical projects. Lead and mentor electrical design teams.

A global biotech company in Maidenhead is hiring a GMP Auditor to ensure compliance with quality standards within their audit program.

We are looking for an experienced auditor who can navigate manufacturing environments and work collaboratively with stakeholders to develop corrective actions that ensure long-term systemic stability.

A global leader in life sciences is seeking an OT Systems Administrator Specialist to support operational technology systems in Slough.

A leading pharmaceutical company in Slough is seeking an analytical testing professional to perform quality assessments on therapeutic proteins.

Collaborate effectively with internal and external stakeholders, demonstrate reliability and flexibility (including on-call duties), and operate warehouse equipment as required. Previous experience in a GMP warehouse environment is advantageous. Familiarity with SAP or other Warehouse Management Sys

QA Associate Location: Windsor, UK Contract: 6-month initial Fixed-Term Contract Industry: Pharmaceuticals About the Role We are seeking a QA Associate to join the Quality Assurance team at a pharmaceutical production site based in Windsor. This is a 6‑month initial fixed-term contract, ideal for someone with previous pharmaceutical experience and a good understanding of GMP who is looking to build or strengthen their QA background. Key Responsibilities • Support the QA team with day-to-day quality activities on site, • Assist with GMP documentation, including SOPs, deviations, and quality records, • Support batch record review and release activities, • Participate in investigations, CAPAs, and change control processes as required, • Ensure activities are performed in compliance with GMP, company procedures, and regulatory standards, • Work cross-functionally with Production, QC, and other site teams Skills & Experience Required • Previous experience in a pharmaceutical or regulated life sciences environment, • GMP experience is essential, • Previous experience in a Quality Assurance role, • Strong attention to detail and good documentation skills, • Ability to work effectively in a fast-paced, regulated environment What’s on Offer • 6-month fixed-term contract with the opportunity to gain valuable pharmaceutical QA experience in a reputable company, • Exposure to a regulated, GMP-compliant manufacturing environment, • Supportive team and hands-on learning opportunities If you are a QA professional with GMP experience looking for a contract opportunity within the pharmaceutical industry, we would be pleased to hear from you

Job title: Scientist (QC Product Testing and Stability) Location: Slough Contract Length: 12 months Working Hours: 37.5 hours/week Pay: 17.96ph About the Role The role is predominantly lab based for the execution analytical testing e.g. HPLC (size exclusion, ion exchange etc.), electrophoresis (e.g. CE SDS, icIEF), spectrophotometry and general characteristic analysis (e.g. visual appearance, pH, Osmolality) for the purpose of assessing the quality and stability of therapeutic proteins. All work is expected to be carried out in a safe and compliant manner in accordance with local EHS policies and cGMP guidelines. In addition, some time will be spent technically reviewing other analysts assays, writing stability study protocols and data summary reports, SOP updates, and assisting with quality records. Key Responsibilities Performs experimental work independently in accordance with SOPs and study protocols on a variety of sample types Performs work in a safe, compliant manner, ensuring training profile is maintained and up to date at all times. Plans and completes assigned tasks within the required timeframe. Communicates progress and escalates challenges to Line Manager and/or scientific lead as appropriate Technically review assays against SOPs, protocols and GMP principles and liaise with operators and study directors to close out technical review of assays. Interpret data against specifications, critically assess results and identify trends within data, reporting any observations and concerns to QC management, SDs, QC representative in a timely manner. Writes stability study protocols, reports, testing summaries etc. Act as a mentor and/or trainer to newer or more junior members of the team and provide help and support to team mates Supports improvement projects within the department and encourages best practice and corrects incorrect/bad practice Support, as needed, with the timely completion of investigations, deviations, CAPAs and change controls and may independently lead and complete minor investigations e.g. pipette calibration failure, storage equipment temperature excursions Actively contributes to QC department general lab housekeeping, ensuring the laboratory is adequately stocked with reagents and consumables as needed. In addition, perform monitoring and maintenance of equipment and may take on system owner responsibilities Work collaboratively in a team to ensure business, regulatory and customer needs are met. Perform other duties as assigned. Education/experience Required: BSc in relevant scientific discipline or relevant previous experience - Chemistry / Biochemistry Experience - GMP, Pharmaceutical, Biological Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy

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

A leading pharmaceutical company in the United Kingdom is seeking a highly motivated Manufacturing Technician.This role entails operating and maintaining manufacturing equipment, ensuring adherence to safety and quality standards, and supporting production efficiency.Candidates should have a High Sc

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.

Candidates should have experience in a GMP environment, attention to detail, and good communication skills.

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

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.

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

In this entry-level role, you will gain hands-on experience in GMP manufacturing, implement safety and production protocols, and contribute to continuous improvements in the production process.

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

You’ll be part of our GMP Data Solutions team, the specialists behind the delivery and implementation of GMP equalisation and rectification projects. Senior Project Analyst - GMP Data Solutions.

This role supports training compliance and competency activities in a fast-paced GMP manufacturing environment.

Elix Sourcing Solutions is looking for a Production Supervisor in Prudhoe to lead a team of approximately 20 staff in a fast-paced manufacturing setting.This hands-off supervisory role emphasizes productivity, quality, and safety improvements with great progression opportunities.Suitable candidates

GMP Recruitment Agency Limited are proud to be partnered with a well-established ad vastly successful Estate Agency based in the Forest of Dean.

A leading pharmaceutical company based in Derby is seeking a Project Manager to oversee multiple projects in pharmaceutical storage and distribution.The successful candidate will ensure compliance with GxP standards and drive continuous improvement through LEAN principles.Essential qualifications in

This key leadership role requires proven expertise in GMP-regulated environments, focusing on production output, team management, and compliance.

A leading biotechnology firm in the UK seeks a QC Analytical Scientist to oversee testing of gene therapy products, adhering to EU and FDA GMP requirements. Ideal candidates will have a degree in Human Health or Sciences and prior experience in a GMP environment.

A leading pharmaceutical manufacturer in the UK seeks a Multi Skilled Engineer.This permanent position involves supporting the maintenance team with breakdowns and scheduled activities.Ideal candidates will have a minimum City & Guilds qualification with significant maintenance engineering experienc

The role requires adherence to GMP standards and involves managing service contractors and vendor relationships.

The role involves operating filling and packing equipment in a GMP environment, ensuring compliance with quality standards.

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

A UK-based innovation organization is seeking an experienced IT Director to lead their technology strategy.This role will enhance digital platforms and ensure compliance with cybersecurity regulations.Responsibilities include overseeing IT operations across multiple sites, leading a team, and aligni

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

Preferred candidates will have experience in GMP environments and possess strong attention to detail and IT skills.