Biotechnology Jobs

Senior QA Specialist, Pharmaceutical Development Quality Assurance (Maternity Leave Cover / Home Based)

This role involves ensuring the quality and compliance of Investigational Medicinal Products (IMPs) developed and manufactured by contract partners. The Senior QA Specialist will lead batch reviews, manage product stability programs, conduct vendor audits, and maintain quality systems in line with cGMP standards. The position supports clinical trial supply readiness and regulatory compliance across the pharmaceutical development lifecycle.

Jazz Pharmaceuticals London, United Kingdom

Remote Contract

CMC Leader (Director)

Leads end-to-end CMC strategy and execution for a pharmaceutical product from early development through commercialisation, including process development, regulatory filings, and lifecycle planning. Coordinates cross-functional global teams across R&D, supply chain, and regulatory to deliver clinical and commercial supply, ensuring technical transfer, quality compliance, and launch readiness. Focuses on complex modalities such as small molecules and oligonucleotides, with strong emphasis on regulatory strategy, risk management, and transition to commercial operations.

GSK Stevenage, United Kingdom

Hybrid Permanent

CMC Leader (Director)

Leads the development, industrialization, and lifecycle delivery of a physical medicine from early development through commercialization, ensuring seamless transition across stages. Coordinates cross-functional CMC and supply chain teams to deliver regulatory filings, process validation, and launch readiness, with a focus on complex products including small molecules and oligonucleotides. Drives strategic decision-making across R&D, manufacturing, and commercial functions to ensure timely, compliant, and scalable product supply.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Senior Specialist I, QA Clinical

The Senior Specialist I, QA Clinical is responsible for quality oversight in clinical development, supporting cross-functional relationships and ensuring compliance with GCP/GVP regulations. Key responsibilities include developing and implementing risk-based audit plans, conducting audits, and managing quality events. The role involves working closely with clinical project teams and external stakeholders, and maintaining the quality management system.

Autolus Stevenage, United Kingdom

Hybrid Permanent Flexible

Senior Counsel

The Senior Counsel provides comprehensive legal support and advice to AstraZeneca's UK marketing company, focusing on AI, data privacy, and commercial matters. They will act as a subject matter expert, draft and review legal documents, and ensure compliance with regulations and internal policies.

AstraZeneca London, United Kingdom

On-site Permanent

Quality Assurance Officer (Pharmaceutical GMP)

This role involves ensuring pharmaceutical products are manufactured and released in compliance with GMP standards, managing quality systems such as deviations, CAPAs, and change controls, and supporting audits and supplier qualification. The Quality Assurance Officer will work closely with Production, QC, and other departments to maintain and improve the Quality Management System. It offers broad exposure to QA processes within a growing specialist manufacturer of CBD APIs and hemp derivatives.

BSPG Laboratories Ltd Great Stonar, Kent, United Kingdom £29,000 – £35,000 pa

On-site Permanent

Pharmaceutical Regulatory Affairs Officer

This role involves managing regulatory submissions and product lifecycle compliance for pharmaceutical products, with a focus on packaging, labelling, and interactions with the MHRA. The candidate will coordinate eCTD submissions, support variations, and ensure change control processes are followed across cross-functional teams. It's a hands-on position offering impact in a regulated environment with hybrid working and a clear regulatory focus.

Evolve Selection Leicester, Leicestershire, United Kingdom £40,000 – £50,000 pa

Hybrid

Quality Assistant (Pharmaceutical)

This role involves supporting quality control and assurance in a pharmaceutical environment, with a focus on microbiological environmental monitoring of cleanrooms and aseptic suites. The candidate will perform testing, document results, and ensure compliance with GMP standards, working closely with internal teams in a fast-paced, deadline-driven setting.

ITH Pharma Middlesex, London, UB8 3QX, United Kingdom £30,073 pa

On-site Permanent

Regulatory Affairs Specialist - Medical Devices

This role involves leading quality assurance and regulatory affairs initiatives within a global medical devices company, working across European, American, and Asian regulatory standards. You will develop and implement solutions for compliance and management systems in a highly technical R&D and manufacturing environment. The position offers exposure to emerging regulated industries and complex, international projects.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom £42,000 – £46,000 pa

On-site Permanent

Regulatory Affairs Specialist

This role involves maintaining technical documentation and ensuring compliance with UK and EU MDR regulations for Class I and IIa medical devices. The specialist will support regulatory submissions, post-market surveillance, and quality management system development within a regulated environment. Collaboration with the QA Manager and ongoing product lifecycle support are key aspects of the position.

Cure Talent Upper Marlbrook, Worcestershire, B61 0RT, United Kingdom £45,000 – £50,000 pa

On-site Permanent

Regulatory Affairs Specialist - Medical Devices - Cambridge

This role involves providing regulatory expertise to guide product development across medical and non-medical technologies, ensuring compliance with international standards such as ISO 13485, FDA 21 CFR 820, and ISO 9001. The specialist will work embedded within project teams, interpreting evolving regulations, supporting quality systems, and enabling innovation while maintaining regulatory alignment throughout the product lifecycle.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Manufacturing Engineer

This role involves designing and optimising high-precision manufacturing processes for patient-specific medical devices, with a focus on scalability and repeatability. The engineer will work extensively with 5-axis CNC systems and CAM software to improve machining efficiency and process stability, while implementing rigorous quality assurance and continuous improvement practices. The position supports global manufacturing expansion and demands a disciplined, data-driven approach to production excellence.

Reed Specialist Recruitment United Kingdom £50,000 – £90,000 pa

On-site Permanent

QA/ Validation Supervisor, Pharmaceutical

This role involves leading a small QA team, ensuring compliance with regulatory standards, and overseeing quality systems and validation activities. Responsibilities include report writing, internal and external audits, and driving continuous improvement initiatives.

NMS Recruit Ltd t/a Russell Taylor Group Walkden, Manchester, M28 3DR, United Kingdom £40,000 – £45,000 pa

On-site Permanent

QA/RA Manager

This role involves leading the design and implementation of regulatory and quality management systems for a portfolio of Class I medical devices, ensuring compliance with ISO 13485 and 21 CFR 820. The candidate will oversee digital EQMS deployment, lead audits, manage post-market surveillance, and build a distributed team while embedding a proactive compliance culture across R&D, supply chain, and commercial functions.

SRG London, United Kingdom

Hybrid Permanent

GLP/GCLP Vendor Oversight and QA Lead (EU)

This role involves leading the quality oversight of external partners in R&D and regulated activities, managing the vendor lifecycle from due diligence to continuous improvement, and ensuring compliance with GLP/GCP/GMP/GVP standards. The position requires close collaboration with various departments to maintain high-quality standards and regulatory compliance.

CSL United Kingdom

On-site Permanent