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Job Location Weybridge Job Description Procter & Gamble (P&G) is a leading global consumer goods company, with Personal Health Care brands including Vicks, Pepto‑Bismol, and Seven Seas. We are seeking a Qualified Person (QP) / Senior Quality Assurance Manager to lead quality and compliance activities across GMP, GDP and HACCP for food supplements and help safeguard consumer trust across our UK Personal Health Care portfolio. If you thrive at the intersection of regulatory excellence, safety, and quality leadership, this role could be your next career step. You will play a key part in ensuring products are manufactured, released, and distributed in full alignment with UK regulatory requirements and global quality standards. In this highly visible role, you will safeguard product quality, protect consumers, and act as a trusted partner to internal teams, suppliers, and regulatory authorities, making a real impact from manufacturing through distribution. *This position will be primarily based in Weybridge (Surrey), with alternative options available in Reading or Skelmersdale. Candidates must be flexible to travel periodically to the Skelmersdale site as required. Role overview As the Qualified Person (QP) for Procter & Gamble UK, you will be accountable for ensuring that products are manufactured, tested, released, and distributed in full compliance with UK legislation and global quality standards. With us, you will: • Act as Qualified Person for Procter & Gamble UK in accordance with UK legislation for Medicinal Products for Human Use, ensuring batch certification, release, and maintenance of the certification register., • Ensure robust GMP, GDP, and HACCP compliance through effective documentation systems, quality and technical agreements, vendor qualification and auditing, and alignment with Marketing Authorisations and Global Healthcare procedures., • Lead quality governance activities, including deviation management, CAPA definition and tracking, quality performance monitoring, and continuous improvement initiatives., • Manage critical quality events such as incidents, complaints, recalls, and withdrawals, acting as the key interface with internal stakeholders, authorities, and drug and food safety bodies., • Prepare for and manage regulatory inspections and approve and oversee annual training plans to ensure personnel are appropriately trained and qualified. What we offer you: • Meaningful Work from Day 1: From Day 1, you’ll step into a role with real accountability where you will directly influence product release, quality outcomes and regulatory confidence for P&G’s UK portfolio, using your expertise to protect consumers and uphold trusted brands. You will be owning your part of the business and helping it grow, with continuous and supportive coaching from your manager and the wider team., • Competitive Benefits: P&G take a Total Rewards approach meaning on top of your competitive salary, which is reviewed annually, you can expect a whole range of benefits including: a double-matched pension scheme, private health insurance, participation in a stock ownership scheme, 25 days holiday and your very own ‘Flex4Me’ Fund which enables you to allocate a portion of your benefits package to the areas that matter most to you., • Flexibility: We operate a flex at work approach, with flexibility built into the role. Our teams spend 3 days of their week collaborating together in our offices or at our external partners. This is balanced with 2 of their days spent on focused work which most tend to do from home. Of course, we do a bit of both every day, but we encourage our teams to choose where they work based on the jobs to be done. Job Qualifications What you’ll bring • Degree in pharmacy or another formal qualification in medicine, veterinary medicine, chemistry, pharmaceutical chemistry and technology or biology., • Registration and approval as a Qualified Person with British Authorities in accordance with local regulations., • Sufficient experience as a Qualified Person under UK regulations and solid experience in Quality Assurance., • Advanced knowledge of GMP and GDP requirements., • Fluency in English, both written and spoken, • Strong communication and collaboration skills with internal teams, suppliers, and regulators., • A results‑driven, quality‑focused mindset with a strong sense of ownership., • Proactivity, organization and ability to operate with urgency in a regulated environment. Right to Work: For this role, P&G are willing to provide sponsorship to those who require a visa to live and work in the UK, subject to meeting all the necessary Home Office requirements. Full details on visa restrictions can be found on the Home Office website and immigration rules are subject to change. P&G is legally required to ensure all candidates have the right to work in the UK from Day 1 of their employment. All applicants will therefore be asked to provide evidence of their right to work at the conclusion of the recruitment process as a condition of employment. At P&G #weseeequal We are an equal opportunity employer and value diversity at our company. At P&G we strive to build a culture where everyone feels welcome, included, and able to bring their full selves to work. We ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process. Please click ___ if you require an accommodation during the application process. Please make sure to wait to hear back from us regarding your accommodation before proceeding with the online assessment, we thank you in advance for your patience. Job Schedule Full time Job Number R000144335 Job Segmentation Experienced Professionals Starting Pay / Salary Range

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.

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

• 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

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

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

• 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

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.

System Specialist (DMS / Veeva) Hybrid | Slough | Up to £45,000 | 6-Month Contract The Role We’re supporting a pharmaceutical manufacturing business in Slough who are looking for a System Specialist to support their Document Management System (DMS) as they prepare for a migration to Veeva Vault. This is a hands-on role focused on GMP document control, system coordination, and data clean-up, ensuring all documentation is compliant, up to date, and audit-ready. You’ll act as a key point of contact across QA, Manufacturing, QC, and Engineering — keeping documentation moving and making sure nothing falls behind. What You’ll Be Doing • Managing the end-to-end document lifecycle (creation, review, approval, archive) within the DMS, • Acting as a super user / coordinator for the system (permissions, workflows, document ownership), • Driving document clean-up activities ahead of the Veeva Vault migration, • Monitoring periodic reviews, chasing overdue documents and escalating where needed, • Supporting cross-functional teams to ensure documents are reviewed and approved on time, • Coordinating document translations across global sites, • Providing user support and training on the system, • Supporting system improvements, testing (OQ/PQ), and process optimisation What They’re Looking For • Experience in document control within a GMP pharmaceutical or biotech environment, • Strong understanding of GMP documentation requirements (e.g. SOPs, validation, change control), • Experience using a DMS / eDMS (e.g. Documentum D2, Veeva Vault, MasterControl, TrackWise), • Comfortable managing workflows, approvals, and stakeholder coordination, • Strong attention to detail and ability to manage multiple priorities Nice to Have • Experience supporting a system migration (eDMS / Veeva Vault), • Previous super user / admin experience, • Exposure to regulatory requirements (FDA, EU Annex 11, 21 CFR Part 11) Why This Role? • Opportunity to be part of a Veeva Vault migration project, • High visibility across multiple business functions, • Hands-on role with real ownership and impact If you are interested please apply or send your CV to

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 t...

Electrical Design Lead / Associate Director All potential applicants are encouraged to scroll through and read the complete job description before applying. £100,000 £120,000 Basic + Car Allowance + Bonus + Private Healthcare + Pension + Clear Pathway to Director Sector: Pharmaceutical | Life Sciences | Advanced Manufacturing Location: London, United Kingdom A design-led consultancy delivering high-specification pharmaceutical, biotech and regulated manufacturing facilities is seeking an Electrical Design Lead / Associate Director. This is a senior leadership role with a defined progression route to Director, aligned with the companys expansion across life sciences projects. The Role Lead electrical design on GMP & pharmaceutical projects Oversee LV distribution & standby power systems Design power infrastructure for laboratories & process equipment Lead and mentor electrical design teams Act as senior client interface Contribute to business development & strategic growth Sign off technical deliverables xrnqpay What Theyre Looking For Strong consultancy background (essential) 10+ years electrical building services design Pharmaceutical / life sciences experience Experience in regulated / GMP environments Chartered or working toward IET Leadership ambition aligned to Director progression

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 require

Lonza is seeking a Biotechnologist 1 for their Slough facility, focusing on hands-on experience in a GMP Manufacturing environment.

This entry-level role focuses on providing hands-on experience in a GMP manufacturing environment.

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

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

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

Familiarity with SAP or other Warehouse Management System. GMP-regulated warehouse, playing a key role in supporting site operations and business objectives. We have 2 open headcounts for the warehouse team.

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.

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

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

This role serves as a GMP Auditorwithin our Research & Development Quality audit program, responsible for executing the global audit plan to ensure the accuracy of scientific data and compliance with legal and corporate standards.

A leading biotech company in Greater London is seeking a meticulous QC Materials Technician to support material inspection and release in a GMP-regulated environment. Candidates should possess at least one year of experience in a GxP or GMP setup, along with strong communication skills and proficien

A leading quality management provider in Southall is seeking a quality assurance specialist to conduct audits, maintain quality management systems, and oversee product inspections.The ideal candidate should have a strong understanding of food safety standards, experience in document control, and an

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

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

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

Veolia is looking for an Electrical Maintenance Technician to work mobile across the Southern Region of the UK.The role is pivotal in ensuring compliance with electrical rules, performing maintenance and troubleshooting on various systems including HVAC and Boilers.This position offers competitive p

Our client requires an experienced Pharmacist with GMP experience to start as soon as possible.

This full-time, on-site role involves implementing quality management systems and ensuring compliance with GMP and ISO standards.

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

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.

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

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

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

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

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

Auditor - GMP page is loaded## Auditor - GMPlocations: Seqirus UK - Maidenheadtime type: Full timeposted on: Offerta pubblicata oggijob requisition id: R-274208Quality in a globalized supply chain is a matter of operational resilience as much as regulatory mandate. This role serves as a **GM

A pharmaceutical manufacturing company is seeking a Multi Skilled Engineer for its Holmes Chapel site.This onsite, permanent role involves maintaining pharmaceutical production equipment and ensuring compliance with safety standards.Candidates should have at least 2 years of relevant experience and

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

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

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

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 requires a hands-on problem-solving approach, contributing to key site projects while adhering to GMP standards.