Latest Operations Analyst - Internship Jobs

(Fixed Term) Scientist, Immunogenicity, Bioanalytical and Molecular Assays

This role involves designing and executing bioanalytical and immunogenicity strategies to support mRNA-based therapeutic development. The scientist will lead assay development for clinical programmes using platforms like ELISA, MSD, and cell-based methods, ensuring regulatory compliance and robust data generation. The position emphasizes collaboration across multidisciplinary teams and integration of digital tools and AI to advance Moderna's pipeline.

Moderna Oxford, United Kingdom

On-site Contract

Senior Research Associate, Bioanalytical & Molecular Assays

This role involves developing, qualifying, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and RT-qPCR—to support clinical pharmacokinetic and pharmacodynamic studies within a GCLp-compliant environment. The scientist will work closely with cross-functional teams to ensure robust data generation, maintain regulatory compliance, and integrate emerging digital and automation technologies into workflows. A strong focus on reagent management, assay documentation, and continuous process improvement is central to the position.

Moderna Oxford, United Kingdom

Hybrid Permanent

SERM Medical Director

This role involves leading pharmacovigilance and risk management strategy for GSK’s global pharmaceutical assets, with a focus on patient safety across clinical development and post-marketing phases. The Medical Director will lead safety governance, drive signal detection and risk mitigation, and represent GSK in regulatory discussions. It requires deep expertise in drug safety, cross-functional leadership in a matrix environment, and strategic input into global safety operations.

GSK United Kingdom

On-site Permanent

Senior Director, Future CMC Dossier Strategy

This role leads the strategic transformation of CMC regulatory submissions at GSK, shaping the future of dossier development through innovation in automation, Generative AI, and structured data. The Senior Director will drive alignment across regulatory, development, quality, and technology functions, acting as a key liaison for enterprise-wide initiatives like Project Sonata and ICH M4Q. The position is central to modernising regulatory processes and establishing next-generation submission standards globally.

GSK £141,750 – £236,250 pa

Manager, Oncology Regulatory Strategy

Lead regional regulatory strategy for oncology products across the Rest of World (ROW) region, aligning with global teams to ensure timely submissions, approvals, and commercially favorable labeling. Partner with project teams and health authorities to shape regulatory positions and influence the regional environment. Ensure compliance and effective implementation of regulatory standards throughout the product lifecycle.

Pfizer United Kingdom

Audit Lead

Lead and develop GMP/GDP audit strategy for a key technology area such as sterile biologics or medical devices, ensuring compliance with global regulations and emerging trends. Conduct complex audits across Pfizer facilities, contract manufacturers, and suppliers, while coaching auditors and driving continuous improvement in quality systems. Collaborate with cross-functional teams to assess risks, resolve findings, and prepare for regulatory inspections.

Pfizer London, SW7 2AP, United Kingdom £162,900 – £271,500 pa

Remote Permanent

Head, PV and Regulatory QA

This role leads the global quality and compliance function for pharmacovigilance (PV) systems, ensuring adherence to international regulations and internal standards across clinical safety, regulatory affairs, and medical affairs. The position combines strategic oversight with hands-on operational leadership, including audit strategy, inspection readiness, deviation and CAPA management, and cross-functional GxP guidance. It requires deep technical expertise in PV processes and strong leadership to drive quality across global teams and third-party vendors.

CSL

Head, PV and Regulatory QA

Leads global pharmacovigilance and regulatory quality assurance, ensuring compliance with GVP, ICH, and regulatory standards across clinical safety, medical affairs, and regulatory affairs. Designs audit strategies, manages inspections, and oversees deviation management, CAPA, and change control systems. Provides cross-functional GxP expertise and drives continuous improvement in PV quality systems.

CSL

Clinical Data Strategy, Manager

This role involves leading clinical data strategy planning and execution across Translational Medicine programs, with a focus on designing fit-for-purpose data collection approaches and supporting robust decision-making. The individual will develop Data Strategy Plans, guide trial teams on data oversight, and leverage internal and external data to inform trial design—particularly in Neuroscience. The position requires deep expertise in clinical assessments, data integrity, and cross-functional collaboration in a global, fast-paced environment.

Novartis London, United Kingdom £49,140 – £91,260 pa

Hybrid Permanent

Biomedical Scientist

This role involves supporting the installation, validation, and verification of new laboratory analysers within an NHS clinical chemistry setting. The Biomedical Scientist will ensure equipment meets performance standards, troubleshoot technical issues, and maintain compliance with quality and regulatory requirements. It offers hands-on involvement in a major laboratory transformation project within a modern NHS environment.

Acorn by Synergie Woolstone, Milton Keynes, Buckinghamshire, United Kingdom

On-site Temporary

Embedded Systems Engineer

Embedded Systems EngineerA long-established global manufacturer of high-voltage power solutions used in medical devices, semiconductor equipment, scientific instruments and industrial systems. The organisation operates design and manufacturing facilities across North America, Europe and Asia and partners with leading OEMs developing...

Terry Parris Associates Codmore Hill, West Sussex, RH20 1DQ, United Kingdom

Pharmaceutical Manufacturing Technician

Prepare and compound sterile pharmaceutical products including total parenteral nutrition and chemotherapy in a cleanroom environment, following strict GMP and SOPs. Focus on accuracy, aseptic technique, and timely delivery of life-saving medicines to hospitals. Work within a supportive team with opportunities for accreditation-based progression and a 4-day week shift pattern.

ITH Pharma Middlesex, London, United Kingdom £30,073 pa

Senior Principal Biostatistician

Lead statistical work across clinical trials, developing protocols, analysis plans, and reporting while driving innovative trial designs and methodologies. Collaborate with cross-functional teams including clinical, regulatory, and programming to support data-driven decision-making in drug development. Engage with external stakeholders such as health authorities and scientific communities to advance quantitative sciences in a pharmaceutical context.

Novartis London, United Kingdom

Hybrid Permanent

Pharmaceutical Production Operative

On behalf of our client we have an immediate and exciting opportunity for a Pharmaceutical Production Operative working Monday to Friday. This is an excellent opportunity for ongoing regular work!Benefits:£12.21 + Holiday PayMonday to FridayMorning & Lates28 days holidayWeekly payOpportunities...

KFM Recuitment Kingston upon Hull, East Riding Of Yorkshire, United Kingdom

Chief Digital & Information Officer

Lead digital, data, ICT, and AI strategy at a world-renowned children’s hospital, driving innovation across clinical care, research, and operations. Spearhead the ethical adoption of emerging technologies like Agentic AI, ensuring robust governance, cybersecurity, and data-driven transformation. Collaborate with clinical, research, and operational leaders to deliver measurable improvements in patient, family, and staff outcomes.

The Guardian London, United Kingdom

On-site Permanent