Latest Operations Analyst - Internship Jobs

(Fixed Term) Manufacturing Associate I

Operate production equipment for mRNA vaccine manufacturing in compliance with cGMP and safety standards. Perform routine maintenance, support deviation investigations, and contribute to continuous improvement in a highly regulated, technology-driven environment. Work collaboratively with QA and cross-functional teams to ensure timely batch disposition and operational excellence.

Moderna

On-site Temporary

(Fixed-Term) Manufacturing Associate I

Operate and maintain equipment in a cGMP-compliant, highly automated mRNA vaccine production environment at Moderna's Oxford facility. Perform production operations, support quality assurance, troubleshoot issues, and contribute to continuous improvement initiatives using digital systems and advanced manufacturing technologies. Work within a 2-2-3 rotating shift pattern to ensure reliable, safe, and compliant vaccine manufacturing.

Moderna Oxford, United Kingdom

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, quality, manufacturing, and technology functions, championing initiatives like ICH M4Q and Project Sonata. It involves influencing senior governance, leading change, and building next-generation regulatory processes in a global, science-driven environment.

GSK United Kingdom £193,500 – £322,500 pa

Senior Director, Future CMC Dossier Strategy

Leads the strategic transformation of CMC regulatory submissions at GSK, driving innovation through automation, Generative AI, and structured data. Works cross-functionally to align regulatory strategy with development and enterprise initiatives, including ICH M4Q and Project Sonata. Focuses on modernising the 'CMC dossier of tomorrow' within a global matrix environment.

GSK

Manager, Oncology Regulatory Strategy

This role involves leading and implementing regional regulatory strategies for oncology products in the Rest of World (ROW) region, ensuring alignment with global objectives and commercial goals. The individual will represent the region on the Global Regulatory Strategic Team, manage submissions and approvals, and shape interactions with health authorities. A key focus is ensuring compliance while influencing the regulatory environment to accelerate patient access to medicines.

Pfizer Marlow, United Kingdom

Manager, Oncology Regulatory Strategy

Leads regional regulatory strategy for oncology products across the Rest of World (ROW), ensuring alignment with global objectives and timely submissions to health authorities. Works closely with cross-functional teams and external agencies to shape regulatory pathways, influence policy, and secure commercially viable labeling. Focuses on compliance, risk mitigation, and strategic engagement in a dynamic regulatory environment.

Pfizer Sandwich, United Kingdom

Laboratory Technician - Plant Biology Institute

This role involves hands-on support for plant science research, including cultivating experimental plants under controlled conditions, preparing reagents and media, performing molecular biology techniques like protein extraction and Western blotting, and maintaining sterile tissue cultures. The technician will assist in Agrobacterium-mediated transformations, microbial and plant cell culture, and operate bioreactors, while ensuring rigorous lab maintenance, accurate data recording, and compliance with biosafety and GMO protocols. The position is central to enabling high-throughput, scalable research within a multidisciplinary team focused on sustainable agriculture and plant-based innovation.

Ellison Institute of Technology Oxford, United Kingdom

On-site 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

QA Technician

This role involves supporting batch review and product release activities within a GMP-regulated diagnostics manufacturing environment. The candidate will review Device History Records, ensure documentation compliance, assist with audits, and contribute to CAPA and non-conformance processes. Working within a collaborative quality team, the technician will help maintain high regulatory standards in a global life sciences organisation.

Hays Life Sciences Birmingham, West Midlands (county), United Kingdom £12 – £14 ph

On-site Contract

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

Associate Director, R&D Project Management

Leads the operational delivery of high-impact, global R&D projects within a cross-functional biotech environment. Focuses on strategic planning, budget and timeline management, risk mitigation, and stakeholder reporting. Provides mentorship to junior project management staff and ensures robust project execution across drug research, development, and manufacturing.

CSL

Hybrid Permanent

Biologics Account Manager

This role involves driving clinical demand for respiratory biologics by building strategic relationships with healthcare professionals and multi-disciplinary teams across a defined UK territory. The Account Manager will lead formulary access, support homecare utilization, and collaborate with cross-functional teams to implement account plans in complex secondary care environments. Success requires strong commercial acumen, stakeholder influence, and deep understanding of the NHS commissioning landscape.

AstraZeneca Sheffield, United Kingdom

On-site Permanent

Field Service Technician

This role involves visiting hospitals and healthcare facilities across the UK to perform equipment servicing, preventative maintenance, installations, and basic fault diagnosis. The technician operates from a fully equipped service van and ensures medical devices remain operational through routine checks and on-site support. Emphasis is on customer service, accurate record-keeping, and working independently with occasional overnight stays.

Career Smart Consulting Ltd Aston Clinton, Buckinghamshire, United Kingdom £30,000 – £36,000 pa

Hybrid Permanent

Production Operator

Operate production machinery and perform quality inspections in the manufacturing of life-saving medical devices such as breathing filters. Work within a regulated environment, following strict procedures to meet safety and quality standards while contributing to team production targets. Role includes full training and opportunities for progression within a global life sciences organisation.

Acorn by Synergie Newquay, Cornwall, United Kingdom £13 – £20 ph

FP&A Manager (Clinical and Project Finance)

The FP&A Manager will lead financial planning and analysis for clinical trials and R&D projects, providing strategic business partnering to scientific and operational teams. This role involves driving financial governance, forecasting, and the automation of reporting processes within a growing biotech environment. The individual will play a key part in scaling financial operations to support OMass’s pipeline in rare diseases and immunology.

OMass Therapeutics Oxford, United Kingdom

Hybrid Permanent