Latest Pharmaceuticals Jobs

Senior Audit Lead (EMEA GMP Audit)

This role involves leading and conducting GMP and compliance audits across GSK’s EMEA global supply chain, including internal and external manufacturing sites, R&D, and logistics providers. The Senior Audit Lead will assess quality, compliance, and technical risks in sterile, biopharm, and vaccines manufacturing environments, deliver clear audit reports, and support senior management with risk mitigation. The position requires subject matter expertise in sterile manufacturing and strong engagement with high-level stakeholders across regulated markets.

GSK €78,750 – €131,250 pa

Senior Audit Lead (EMEA GMP Audit)

Lead and conduct GMP and compliance audits across GSK's EMEA biopharm, vaccines, and pharmaceutical manufacturing network, including internal and external sites. Provide sterile manufacturing expertise, manage complex stakeholder relationships, and deliver objective audit reports to support risk mitigation and regulatory compliance. The role involves up to 40% travel across European sites.

GSK €73,050 – €121,750 pa

On-site Permanent

Technical Service Engineer

This role involves providing on-site and remote technical support for advanced robotics solutions used in pharmaceutical and biotechnology laboratories. The engineer will perform preventative maintenance, troubleshoot complex systems, and act as a subject matter expert for customers, using tools like D365 and remote diagnostics. The position requires strong problem-solving skills, customer engagement, and occasional travel beyond the Manchester base.

Wallace Hind Selection Wa27Tt, United Kingdom £52,000 – £56,000 pa

Technical Service Engineer

This role involves providing on-site and remote technical support for advanced robotics solutions used in pharmaceutical and biotechnology environments. The engineer will perform preventative maintenance, troubleshoot complex systems, and act as a subject matter expert for customers, using tools like D365 and RMA systems. The position includes 24/7 on-call responsibilities and extensive training in cutting-edge automation technologies.

Wallace Hind Selection Bl21Be, United Kingdom £52,000 – £56,000 pa

On-site Permanent

Vaccines Safety Sciences Lead

Leads and manages pharmacovigilance safety sciences functions, ensuring compliance with global regulatory standards and overseeing signal detection, safety data analysis, and process optimization. Provides strategic direction for evolving PV legislation and acts as a subject matter expert in audits and inspections. Supports drug development and post-marketing safety reporting while driving data visualization and analytical improvements.

CSL

Hybrid Permanent

Vaccines Safety Sciences Lead

Leads vaccine safety sciences functions, ensuring compliance with pharmacovigilance regulations and global safety standards. Oversees signal detection, safety data analysis, and regulatory documentation while guiding process improvements and cross-functional initiatives. Manages teams and supports regulatory inspections, safety reporting, and the implementation of data visualization tools for enhanced decision-making.

CSL

Hybrid Permanent

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading and executing phase-appropriate bioanalytical strategies for immunogenicity and ligand binding assays (LBA) within Moderna’s mRNA-LNP therapeutic pipeline. The Principal Scientist will oversee assay development, validation, and sample analysis, ensuring regulatory compliance and scientific rigor across clinical programs. The position emphasizes collaboration with cross-functional teams, integration of emerging technologies including AI-enabled tools, and contribution to regulatory submissions and data interpretation in a GcLP-compliant environment.

Moderna Oxford, United Kingdom

Hybrid Permanent

Sr. Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays

This role involves developing, validating, and executing ligand-binding and cell-based assays to support mRNA medicine development. The candidate will generate pharmacodynamic and immunogenicity data in a regulated GcLP environment, manage critical reagent characterization, and contribute to clinical sample testing using Watson LIMS. The position emphasizes scientific rigor, regulatory compliance, and collaboration within a high-performance team advancing novel bioanalytical assays.

Moderna Oxford, United Kingdom

Hybrid Permanent

Executive Regulatory Science Director, Respiratory & Immunology

Lead global regulatory strategy for respiratory and immunology therapies across development stages, from early research to commercialization. Provide expert guidance on regulatory pathways, engage with health authorities, and mentor regulatory leaders. Shape policy and ensure compliance while advancing innovative treatments through key milestones and approvals.

AstraZeneca

Global Clinical Head, Respiratory

Lead clinical strategy and scientific oversight for a respiratory product within a global pharmaceutical team, driving late-phase clinical development, regulatory submissions, and benefit/risk assessments. Responsible for cross-functional leadership, mentoring clinical teams, and aligning clinical components of the Target Product Profile and development plans. Engages with regulatory agencies and commercial stakeholders to shape global scientific and medical direction.

AstraZeneca Cambridge, United Kingdom

GCP Compliance Director (Program & Study)

Lead a team of GCP Compliance Managers to ensure global clinical trials adhere to Good Clinical Practice and regulatory standards. Drive inspection readiness, audit oversight, and quality issue management across clinical development programs. Shape compliance strategy and foster a culture of quality and continuous improvement within a matrixed pharmaceutical environment.

Novartis London, United Kingdom £83,510 – £155,090 pa

Hybrid Permanent

GCP Compliance Manager (GCO)

This role involves overseeing global clinical operations compliance with Good Clinical Practice (GCP) standards, managing quality issues, leading audit and inspection readiness, and driving self-assessments to ensure regulatory adherence. The professional will coordinate cross-functional risk assessments, lead investigations, and provide expert guidance across complex, multi-study environments. It emphasizes structured compliance frameworks, patient safety, and data integrity within a hybrid working model.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Field Service Engineer, Water Treatment

Field Service EngineerMedical and Laboratory based Water Treatment SystemsNO WATER TREATMENT EXPERIENCED REQUIRED; JUST A GOOD ELECTRICAL-MECHANICAL SERVICE OR REPAIR BACKGROUNDGloucester, Cheltenham, and WorcesterExcellent Earnings Including "door to door'" Overtime (£45K-£50K) + Company Vehicle + Excellent benefits package including Healthcare,...

TRS Consulting Innsworth, Gloucestershire, United Kingdom £45,000 – £50,000 pa

Document Controller

Job Title:Document Control SpecialistLocation:ThornabySalary:£30,000 - £35,000 DOEBenefits:* Competitive salary* Excellent benefits package* Ongoing training and development* Career progression opportunities* Collaborative and supportive working environment* Opportunity to work within a highly regulated manufacturing environmentThe Company:Our client is a leading manufacturer operating...

Theo James Recruitment Thornaby-on-Tees, North Yorkshire, TS17 9BT, United Kingdom £30,000 – £35,000 pa

Product Manager

Product ManagerCambridgeUp to £70,000 + benefitsRole Overview: Product Manager:The company is looking for a technically competent Product Manager to lead global commercial and strategic activities for their range of scientific products used in the food & beverage markets. The role...

Marcus Webb Associates Limited Cambridge, Cambridgeshire, United Kingdom £60,000 – £70,000 pa