Latest Operations Analyst - Internship Jobs

Operations Analyst

The Operations Analyst Intern will design and implement AI-driven workflows and automation systems to scale Helical’s internal operations. This role involves building intelligent agents, automating processes using Make.com, managing the SaaS stack, improving onboarding, and supporting finance operations. The intern will work directly with the Chief of Staff and has the potential to transition into a full-time role.

Helical London, United Kingdom

On-site Internship

Analyst, Quality Control, Microbiology

This role involves performing routine environmental monitoring, water sampling, and microbiological testing (including sterility, bioburden, and endotoxin) for mRNA products in a GMP-regulated manufacturing environment. The analyst will support method transfers, data review, investigations, and compliance activities while working closely with internal teams and contract laboratories. Emphasis is placed on digital workflows, data integrity, and adherence to cGMP standards.

Moderna Oxford, United Kingdom

Analyst, Quality Control, Microbiology

This role involves performing routine environmental monitoring, water sampling, and microbiological testing to support GMP quality control for mRNA products. The analyst will execute tests including sterility, bioburden, endotoxin, and TOC, while supporting method transfers, validations, and compliance with cGMP standards. The position requires strong documentation practices, collaboration with cross-functional teams, and active participation in quality systems such as investigations and audits.

Moderna

On-site Permanent

QC Supervisor

This role involves leading a team of QC Analysts in a laboratory environment, overseeing testing of reagents, raw materials, and finished ELISA-based diagnostic products. The supervisor ensures data accuracy, compliance with SOPs and GDP, and supports investigations into deviations while driving process improvements and maintaining audit readiness. Collaboration with R&D and Manufacturing teams ensures consistent product quality and operational continuity.

Cranleigh Scientific Bracknell, Berkshire, United Kingdom

Device and Packaging Technologist

This role provides technical support for device assembly and packaging operations at GSK’s Barnard Castle site, focusing on sterile, intranasal, dermatological, and combination products. The technologist will lead investigations, support new product introductions, drive process improvements, and ensure compliance with GMP and regulatory standards across internal and external manufacturing sites.

GSK Barnard Castle, 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

Director, Clinical Science – Oncology Clinical Development

Lead scientific input into oncology clinical trial design, data interpretation, and regulatory documentation within a global pharmaceutical environment. Contribute to study-level execution and strategic insights while collaborating across multidisciplinary teams. Focus on advancing cancer therapies with high unmet need through rigorous clinical science and cross-functional partnership.

GSK Stevenage, United Kingdom PLN 472,500 – PLN 787,500 pa

Hybrid Permanent

Analytical Chemist, Pharmaceutical (HPLC) 12 month fixed term

Perform analytical and stability testing of pharmaceutical and nutraceutical products using HPLC, GC/MS, and wet chemistry techniques in a GMP-regulated environment. Responsibilities include data entry into LIMS, equipment calibration, troubleshooting, and supporting audit readiness. The role also involves training junior staff and contributing to quality investigations and cross-laboratory support.

NMS Recruit Ltd t/a Russell Taylor Group Swadlincote, Derbyshire, DE11 0AG, United Kingdom £30,000 – £33,956 pa

On-site Contract

Technical Product Owner

This role involves owning and prioritising a product backlog while working closely with engineering teams to translate complex business requirements into deliverable technical solutions. The Technical Product Owner will use SQL for data analysis, contribute to system design discussions involving APIs and data models, and create solution artefacts such as UML diagrams. As the team grows, there is an expectation to mentor business analysts and help shape the product function’s evolution within a regulated life sciences environment.

Leo Technology London, United Kingdom £70,000 – £90,000 pa

Mass Spectrometry Technician

This role involves hands-on operation and maintenance of GC-MS and LC-MS systems to support metabolomics research in plant science. The technician will prepare biological samples, conduct high-quality mass spectrometry analyses, process and interpret data using bioinformatics tools, and provide technical support to researchers. Emphasis is placed on precision, collaboration with scientists, and ensuring reliable instrument performance within a multidisciplinary, innovation-driven environment focused on global food security and sustainability.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

Regulatory Scientist

Supports regulatory strategies for gene therapies, focusing on post-approval lifecycle management in EU/UK markets and expansion in ROW regions. Prepares and reviews submissions, manages labelling updates, and responds to regulatory queries. Monitors regulatory intelligence and contributes to SOPs and audit readiness.

Orchard Therapeutics London, United Kingdom

Hybrid Permanent

Associate Director, Clinical Trial Disclosure & Transparency

This role leads global clinical trial disclosure and transparency strategy, ensuring compliance with international regulations such as FDAAA, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while guiding cross-functional teams and managing vendor performance. They also support redaction of confidential information and drive process improvements across disclosure operations.

CSL United Kingdom

Associate Director, Clinical Trial Disclosure & Transparency

This role leads global clinical trial disclosure and transparency strategy, ensuring compliance with international regulations such as FDAAA 801, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while managing redaction of confidential information for public release. They act as a key liaison with regulatory bodies and internal teams, driving process efficiency and vendor performance across the clinical development lifecycle.

CSL

Medical Safety Lead - CRM

The role involves monitoring clinical safety data, conducting medical assessments of adverse events, and identifying safety signals using both individual and aggregate data. The Medical Safety Lead will apply AI-enabled tools to enhance pharmacovigilance processes and provide critical medical input into regulatory submissions and safety documentation. Collaboration with global cross-functional teams is central to integrating safety insights across drug development programs.

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

Operations Lead

Lead end-to-end manufacturing, logistics, and warehouse operations within a regulated life sciences environment, driving performance in safety, quality, delivery, and cost. Champion lean principles and continuous improvement while developing teams and supporting new product introductions and site expansion initiatives.

Hays Procurement Jobs Llantrisant, Mid Glamorgan, United Kingdom £75,000 – £85,000 pa

On-site Permanent