Latest Pharmaceuticals Jobs

Buyer - Pharmaceuticals

This role involves managing procurement activities, supplier relationships, and quality management within a regulated pharmaceutical manufacturing environment. You will work closely with the Manufacturing, Quality, and Operations teams to ensure effective sourcing and compliance with GMP standards.

Cranleigh Scientific Ditton, Kent, ME20 6AE, United Kingdom £22,800 – £28,800 pa

Hybrid Flexible

Production Manager - Pharmaceuticals

Lead and manage pharmaceutical manufacturing operations, ensuring compliance with GMP and regulatory standards while driving safety, quality, and continuous improvement. Oversee production scheduling, KPIs, and cross-functional collaboration with engineering, quality, and supply chain teams. Implement Lean Manufacturing principles and operational efficiencies within a growing, regulated environment.

Smart4Sciences Nottingham, Nottinghamshire, United Kingdom

On-site Permanent

Operations Manager - Pharmaceuticals

Operations Manager - PharmaceuticalsI am currently recruiting for an Operations Manager to work within the pharmaceutical industry, for a niche, yet established product, this is a great opportunity for a Production Manager to work standard hours and develop their skillset...

Smart4Sciences Nottingham, Nottinghamshire, United Kingdom

QC Analyst – Pharmaceuticals

This role involves performing routine and non-routine analysis of raw materials and finished pharmaceutical products using techniques such as HPLC, GC, UV, and FTIR. The analyst will lead Out of Specification investigations, ensure compliance with GMP standards, and contribute to method development and validation. It is a site-based laboratory position requiring strong documentation, troubleshooting, and analytical skills in a regulated environment.

RBW Consulting New Malden, London, KT3 3JQ, United Kingdom

On-site Permanent

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

Research Associate, Compound Management

The Research Associate will manage inventory, prepare reagents, and run automated systems for high-throughput screening. They will collaborate with cross-functional teams to optimize workflows and adopt new technologies, contributing to the company's drug discovery platform.

Recursion United Kingdom

On-site Permanent

Compound Management Inventory Specialist (Contractor)

This role involves managing compound inventory and supporting high-throughput screening by preparing precise compound plates through automated systems. The specialist will maintain organization across multiple storage locations and ensure accurate, efficient fulfillment of experimental requests in a fast-paced, tech-driven drug discovery environment.

Recursion United Kingdom

On-site Contract

Chemical Process Operator

This role involves operating chemical process plant and manufacturing equipment, following batch manufacturing instructions, monitoring chemical reactions, and supporting material handling and packaging activities. The position offers long-term stability and development opportunities within a safety and quality-driven manufacturing environment.

Talent STEM Ltd Stradishall, United Kingdom

On-site Permanent Shift-work

Business Development Manager in Medtech & Life Sciences

This role involves driving market entry and growth strategies for international medtech and life sciences clients in Japan. The Business Development Manager will lead the full sales and licensing cycle, identify partners and customers, and provide cultural and commercial insights to support cross-border business development. The role requires frequent client engagement, reporting, and on-the-ground support for client visits, with a strong focus on communication and relationship-building in a hybrid working environment.

Centre People Appointments Tokyo, United Kingdom JP¥6,000,000 – JP¥7,000,000 pa

Hybrid Permanent

Head of Medtech and Life Sciences

This role involves leading market entry, sales, and licensing projects for international healthcare clients in Japan’s MedTech and life sciences sectors. The candidate will manage a local team, drive commercial initiatives from lead generation to deal closure, and provide strategic sector insights. Emphasis is placed on building cross-sector relationships and developing business infrastructure to support growth in biotech, medical devices, IVD, and digital health.

Centre People Appointments Tokyo, United Kingdom JP¥12,000,000 – JP¥14,000,000 pa

On-site Permanent

Regulatory Affairs Assistant

The Regulatory Affairs Assistant will provide administrative, operational, and compliance support to the Regulatory Affairs team, ensuring accurate data and documentation, supporting team processes, and maintaining compliance with regulatory standards. The role involves a broad range of activities, including regulatory file compilation, database management, project coordination, and administrative support to the Head of Regulatory and the team.

AstraZeneca London, United Kingdom

On-site Permanent

Process Technologist

As a Process Technologist, you will support the production area by providing technical services, troubleshooting, and working on technical projects. You will collaborate with cross-functional teams to ensure product quality and compliance, execute process validation, and perform root cause analysis for material and processing issues.

GSK Barnard Castle, United Kingdom

On-site Permanent

Director, Quality Assurance (Diagnostics & Devices)

Director, Quality Assurance (Diagnostics & Devices)Cambridge, UK (3 days on site per week)About AstraZenecaAstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases....

AstraZeneca Cambridge, United Kingdom

Therapy Supply Chain Manager

Leads end-to-end supply planning and execution for a designated therapy area, ensuring uninterrupted patient access to medicines. Works cross-functionally across planning, manufacturing, quality, and commercial teams to resolve supply disruptions, drive inventory optimisation, and implement continuous improvement initiatives using data analysis and planning systems. Focuses on risk mitigation, regulatory compliance, and performance monitoring within a global pharmaceutical supply chain.

GSK United Kingdom

Hybrid Temporary

Quality Officer (GDP) - Midlands

This role involves ensuring compliance with Good Distribution Practise (GDP), ISO 9001, and ISO 13485 standards through quality assurance support across operational and supplier processes. The Quality Officer will manage change controls, deviations, CAPA, audits, and KPI reporting while maintaining the Quality Management System. Responsibilities include supporting client onboarding, complaint investigations, and regulatory readiness in a healthcare or life sciences environment.

Adecco United Kingdom £37,000 – £42,000 pa

Hybrid Permanent