Latest Pharmaceuticals Jobs

Quality Manager (m/f/x) - EU-based

The Quality Manager role involves maintaining and improving CSL's Affiliate Quality Management System across Europe and global affiliates. Responsibilities include inspection readiness, quality system governance, process harmonization, and supporting global quality initiatives. The role requires collaboration with multiple functions and stakeholders, including Quality, Regulatory Affairs, and Commercial Operations.

CSL Haywards Heath, United Kingdom

Quality Manager (m/f/x) - EU-based

The Quality Manager role involves maintaining and improving CSL's quality management systems across Europe and global affiliates. Responsibilities include inspection readiness, process harmonization, and supporting quality initiatives. The role requires strong knowledge of pharmaceutical regulations and quality systems, with a focus on collaboration and continuous improvement.

CSL

Associate Director, CMC Regulatory Affairs, International

This role involves leading CMC regulatory strategies and submissions for international markets, with a focus on mRNA-based products across vaccines, oncology, and rare diseases. The individual will guide global regulatory compliance, interact with health authorities, and support manufacturing and quality teams through regulatory interpretation and change control. It requires deep expertise in CTD-format filings and a proactive approach to managing multi-therapeutic regulatory programs in a fast-paced environment.

Moderna

On-site Permanent

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

Develops and validates ligand-binding and cell-based assays to support clinical programs for mRNA medicines. Performs pharmacodynamic and immunogenicity testing in compliance with GcLP, using platforms like Thermo Watson LIMS. Contributes to assay development, reagent management, and regulatory documentation in a fast-paced, innovative lab environment.

Moderna

Hybrid Permanent

SERM Medical Director

Provides medical and scientific leadership in the safety evaluation and risk management of GSK’s oncology assets in clinical development. Interprets safety data, identifies and escalates safety signals, and delivers evidence-based recommendations to support benefit-risk decisions. Engages with global governance, regulatory authorities, and cross-functional teams to shape the safety profile of innovative oncology medicines.

GSK €119,250 – €198,750 pa

On-site Permanent

SERM Medical Director

Provides medical and scientific leadership in the safety evaluation and risk management of GSK’s oncology assets in clinical development. Interprets safety data, identifies and escalates safety signals, and delivers evidence-based recommendations to inform benefit-risk decisions. Engages with global cross-functional teams, regulatory authorities, and governance committees to shape the safety profile of innovative oncology medicines.

GSK €81,750 – €136,250 pa

Global Regulatory Associate Director, Life Cycle Management

This role involves managing regulatory maintenance activities for a high-complexity pharmaceutical product portfolio, ensuring compliance and timely submissions to global health authorities. The individual will lead strategic regulatory input across cross-functional teams, respond to complex queries, and support continuous process improvements. It is a hybrid or remote position with a focus on lifecycle management of innovative medicines.

Novartis £67,900 – £126,100 pa

Hybrid Permanent

Field Service Engineer, Medical Diagnostic Systems

Provide on-site service, maintenance, and breakdown repair for advanced medical diagnostic systems used in NHS and private laboratories. Work directly with laboratory staff to resolve technical issues and ensure optimal system performance. Receive full product training and support a market-leading provider of diagnostic equipment.

TRS Consulting Falkirk, Stirling And Falkirk, United Kingdom £52,000 pa

Field Service Engineer, Medical Diagnostic Systems

Perform on-site service and repair of advanced medical diagnostic systems in NHS and private laboratories, ensuring minimal downtime through proactive maintenance and technical troubleshooting. Work closely with lab personnel to deliver reliable diagnostic solutions while receiving full product training. Role involves frequent customer visits and some weekend work as part of a five-day working week.

TRS Consulting Stirling, Stirling And Falkirk, United Kingdom £52,000 pa

Field Service Installation Specialist (UK, IRL)

This role involves performing high-quality installations, relocations, and de-installations of critical medical diagnostic instruments. The Technical Specialist will work closely with internal and external stakeholders, ensuring compliance with safety and quality standards, and contributing to continuous improvement initiatives.

Roche United Kingdom

Bioanalytical Lead, London

Lead the development and execution of bioanalytical strategies for a diverse portfolio of AI-designed therapeutics, including small molecules, biologics, and ADCs. Design and validate PK, PD, and immunogenicity assays, manage global CROs, and integrate bioanalytical data into AI models to refine drug discovery. Play a key role in IND-enabling studies and cross-functional preclinical development in a hybrid London-based role.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Director of Clinical Pharmacology, Cambridge, MA

Lead clinical pharmacology strategy for small molecule programs in oncology and non-oncology areas, designing and executing studies from Phase 1 through late development. Utilize AI-driven models for PK/PD prediction, dose optimization, and regulatory submissions, while managing CROs and translating preclinical data into human dosing strategies.

Isomorphic Labs Cambridge, United Kingdom

Vendor Program Strategy Director - Global Clinical Operations

This role involves developing and executing vendor strategies for clinical programs, aligning vendor needs with program objectives, and driving operational efficiency and value realization. The Director will work closely with clinical teams, procurement, and other stakeholders to ensure effective vendor management and strategic decision-making.

Novartis London, United Kingdom

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Data Solution Architect

The Data Solution Architect designs end-to-end data solutions, including data integration, warehousing, governance, and analytics. They work closely with technical leads and data teams to ensure scalable, secure, and governed solutions, influencing the data architecture of a rapidly evolving biotech company.

Autolus United Kingdom

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Senior Engineer, CSV Validation

This role involves end-to-end ownership of computerised system validation (CSV) for GxP-regulated systems used in the manufacturing and testing of advanced CAR-T cell therapies. The engineer will author and execute validation documentation, ensure compliance with international regulations (e.g. FDA 21 CFR Part 11, EU GMP Annex 11), manage change controls and CAPAs, and support regulatory inspections. The position requires strong technical writing, cross-functional collaboration, and expertise in GAMP 5 and data integrity within a biopharmaceutical context.

Autolus Stevenage, United Kingdom