Latest Pharmaceutical Scientist Jobs

Sr. Data Platform Engineer - Computer System Validator

As a Senior Data Platform Engineer, you will build, scale, and operate a validated data platform with petabyte-scale data, ensuring data integrity and traceability in a GxP-compliant environment. You will collaborate with biologists, chemists, and data scientists to make Recursion’s vast datasets discoverable and queryable, supporting the company’s mission to advance drug discovery through technology and biology.

Recursion United Kingdom £142,500 – £220,500 pa

Hybrid Permanent

Director, Neuroscience (In Vitro Cellular Biology)

This role involves leading the development and application of human iPSC-derived cellular models for neurodegenerative disease drug discovery. You will design and oversee cellular and molecular assays, collaborate with cross-functional teams, and mentor scientists to advance therapeutic discovery.

Recursion United Kingdom £198,000 – £237,600 pa

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across EMEA and other highly regulated markets. You will evaluate compliance with GMP, regulatory requirements, and quality systems, and provide sterile manufacturing expertise. The role requires strong communication and stakeholder engagement skills.

GSK

Hybrid Permanent

Senior Director, Head of Global Medical Governance, ViiV Healthcare

This role involves leading the global medical governance system at ViiV Healthcare, ensuring compliance and ethical standards across all medical activities. Responsibilities include developing and maintaining governance policies, advocating for medical governance, and collaborating with regional teams to embed best practices.

GSK United Kingdom

On-site Permanent

Senior Manager - Engineering & Maintenance

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director at Pfizer will be responsible for developing and maintaining quality plans, ensuring inspection and audit readiness, and providing oversight of process deviations and investigations. This role involves interpreting and applying global regulations, driving compliance, and collaborating with stakeholders to identify and mitigate risks, ensuring the quality and integrity of Pfizer's medicines and vaccines.

Pfizer United Kingdom

On-site Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director will lead the development and maintenance of Quality Plans, ensure inspection and audit readiness, and provide quality oversight of process deviations and investigations. This role involves interpreting and applying regulatory requirements, identifying and mitigating compliance gaps, and driving continuous improvement in pan-regulatory processes and data quality.

Pfizer London, SW7 2AP, United Kingdom

On-site Permanent

Automation Engineer - Pharmaceutical

This role involves maintaining and troubleshooting automation and control systems in a pharmaceutical manufacturing environment, ensuring compliance with GMP regulations. You will participate in computerized system validation, support continuous improvement projects, and collaborate with cross-functional teams.

Smart4Sciences West Yorkshire, United Kingdom

On-site Permanent

Document Manager, Pharmaceuticals

Document Manager - CAPEX Projects (Pharmaceutical Industry) Contract, Outside IR35We are seeking an experienced and detail-oriented Document Manager to support CAPEX (Capital Expenditure) projects within a dynamic pharmaceutical environment. This role is critical in ensuring the effective control, organization, and...

Smart4Sciences Crewe, Cheshire, United Kingdom

Contract

Field Service Engineer

This role involves servicing and maintaining electro-mechanical medical devices in various healthcare settings within the Watford, Enfield, Barnet, and surrounding areas. You will be responsible for fault-finding, equipment maintenance, and providing customer service, with full product training provided.

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

On-site Permanent

Field Service Engineer

The Field Service Engineer will be responsible for servicing, maintaining, and troubleshooting electro-mechanical medical devices across East and North London. The role involves hands-on work in medical environments, providing customer service and ensuring equipment reliability.

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

On-site Permanent

Automation/Process Control Engineer

This role involves strengthening control systems in AstraZeneca's manufacturing network, using digitalization and Lean techniques to improve production speed, resilience, and quality. The engineer will manage small projects, provide technical support, and mentor peers in automation and control systems.

AstraZeneca Macclesfield, United Kingdom

On-site Contract

General Operative

General OperativeLocation: SwindonPay Rate: £13.86 + 22% shift allowanceShift Pattern: Rotating weekly shifts (Early: 07:00-15:00 | Late: 15:00-22:45)We are looking for General Operators to join our production team in Swindon. You will support pharmaceutical manufacturing by following procedures, maintaining a...

Manpower Swindon, Wiltshire, United Kingdom £14 ph

Project Consultant

As a Project Consultant, you will manage client relationships and oversee the delivery of high-quality projects using Patient Cloud technology. Your responsibilities include managing study portfolios, leading cross-functional teams, and ensuring project milestones are met on time and within budget.

Randstad Engineering London, United Kingdom

Instrument Software Validation Analyst

This role involves maintaining validated systems through structured validation processes (IQ/OQ/PQ) and bridging technical software testing with regulatory compliance. Responsibilities include ensuring adherence to FDA, EMA, and GMP regulations, as well as working with laboratory systems like LIMS and Chromatography Data Systems.

Access Computer Consulting Brussels, Belgium £302 – £345 pd

On-site Permanent