Latest Pharmaceuticals Jobs

Quality & Regulatory Co-Ordinator

This role involves maintaining and administering AAH Pharmaceuticals' Quality Management System to ensure compliance with MHRA Good Distribution Practice guidelines and ISO 9001:2015. The coordinator will support audits, manage documentation, and ensure regulatory requirements are met across the business. The position also contributes to continuous improvement and acts as a liaison with customers, suppliers, and regulators.

AAH Pharmaceuticals Warwickshire, United Kingdom

Van Driver

As a Van Driver at Movianto, you will deliver pharmaceutical products efficiently and safely, ensuring compliance with health and safety regulations. You will operate company vehicles, perform daily maintenance checks, and maintain a professional appearance while adhering to legal requirements and company policies.

Movianto St. Helens, United Kingdom £29,467 pa

On-site Permanent

Project Manager

This role involves managing the full lifecycle of industrial automation projects, from initial planning and stakeholder coordination to delivery and technical issue resolution. The Project Manager will act as a central point for cross-disciplinary collaboration, ensuring compliance, quality, and customer satisfaction in complex engineering environments. Key responsibilities include budget and schedule oversight, risk management, change control, and supporting both engineering and sales teams through quotation and commissioning phases.

Automated Industrial Robotics Wakefield, West Yorkshire, United Kingdom

Van Driver

As a Van Driver at Movianto, you will deliver pharmaceutical products efficiently and safely, ensuring compliance with health and safety regulations. You will operate company vehicles, perform daily maintenance checks, and maintain a professional image while adhering to legal requirements and company policies.

Movianto Slough, United Kingdom £29,467 pa

On-site Permanent

QA Technician

This role involves supporting batch review and release activities within a GMP-regulated manufacturing environment, focusing on quality assurance for medical diagnostics. The candidate will review Device History Records, ensure compliance with regulatory standards, manage quality documentation, and assist with audits and CAPA processes. Working within a collaborative quality team, the position plays a key role in maintaining product quality and regulatory compliance.

Hays Life Sciences Birmingham, West Midlands (county), United Kingdom £12 – £14 ph

On-site Contract

Document Controller

Manages controlled documentation and quality records throughout their lifecycle in a regulated medical device manufacturing environment. Supports change control, audit readiness, and compliance with ISO13485, while ensuring accurate, traceable, and timely document availability. Provides operational support for product release by reviewing batch records, device history files, and manufacturing documentation, and may supervise junior team members.

Aurora Life Sciences Leeds, West Yorkshire, United Kingdom £40,000 – £50,000 pa

Operations Lead

Lead manufacturing, logistics, and warehouse operations within a regulated life sciences environment, driving performance in safety, quality, and efficiency. Champion lean principles, continuous improvement, and operational transformation while developing teams and supporting site growth. Play a central role in strategic planning, change management, and cross-functional initiatives including new product introductions and scale-up activities.

Hays Procurement Jobs Llantrisant, Mid Glamorgan, United Kingdom £75,000 – £85,000 pa

Senior Manager, HCC EMEA Regional Office & Risk Management COE – Orthopaedics

This role involves providing strategic healthcare compliance leadership across EMEA for Johnson & Johnson's Orthopaedics business, now transitioning to DePuy Synthes. The Senior Manager will integrate compliance into commercial operations, lead risk management initiatives, and advise regional stakeholders on regulatory and ethical standards. The position requires deep expertise in compliance frameworks, third-party risk, and cross-functional collaboration in a highly regulated, multinational environment.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

NPI Engineer

The NPI Engineer will lead the industrialisation and technology transfer of medical devices from development into controlled manufacturing, ensuring robust, validated processes in compliance with ISO 13485. This role involves cross-functional coordination, process development, equipment specification, and creating manufacturing documentation to bridge design and production. The position offers ownership of end-to-end NPI projects within a growing, innovative medical device company.

Euro Projects Recruitment Shippon, Oxfordshire, United Kingdom £40,000 – £45,000 pa

Senior Manager, HCC EMEA Regional Office & Risk Management COE – Orthopaedics

This role involves providing strategic healthcare compliance leadership across EMEA markets for Orthopaedics, integrating compliance into business decisions and risk management processes. The individual will advise regional leadership, lead risk mitigation initiatives, and align compliance activities with global standards. The position plays a key role in shaping a culture of integrity within a highly regulated medical technology environment.

Johnson & Johnson MedTech Ireland €85,000 – €146,050 pa

Quality Assurance Officer

This role involves reviewing batch manufacturing and packaging records to ensure compliance with GMP standards prior to product release, supporting batch release activities, and collaborating with external manufacturing partners and internal teams. The candidate will maintain quality documentation and ensure adherence to the Quality Management System within a virtual pharmaceutical model. The position offers hybrid working and is part of a supportive Quality team in a growing organisation with a diverse product portfolio.

Walker Cole International London, United Kingdom £30,000 – £35,000 pa

Supplier Quality Officer

This role involves managing the end-to-end supplier quality process for a manufacturer serving highly regulated industries. You will conduct supplier audits (including international travel), ensure compliance with multiple ISO standards, manage supplier performance through KPIs and CAPAs, and collaborate with procurement on supplier selection. The position requires hands-on auditing experience and independent management of quality systems within a critical supply chain context.

hireful Skegness, United Kingdom £35,000 – £40,000 pa

Medical Affairs Coordinator

Talentmark are recruiting for a Medical Affairs Coordinator to join a company in the pharmaceutical industry on a contract basis for 12 months from mid-September 2026.Company:Our client is one of the largest pharmaceutical companies in the world. They focus on...

Talentmark Basingstoke, Hampshire, United Kingdom £15 – £20 ph

Field Service Engineer

This role involves servicing and maintaining electro-mechanical medical devices in various medical environments across Watford, Enfield, Barnet, and surrounding areas. Responsibilities include fault finding, equipment maintenance, and providing customer service. Full product training is provided, and the ideal candidate will have experience with electro-mechanical equipment and a technical qualification.

Redshore Watford, Hertfordshire, United Kingdom £42,000 – £45,000 pa

On-site Permanent

Field Service Engineer

This role involves servicing and maintaining electro-mechanical medical devices in medical environments across East and North London. Responsibilities include fault-finding, equipment maintenance, and providing customer service, with full product training provided.

Redshore London, United Kingdom £40,000 – £45,000 pa

On-site Permanent