Jobs in Reading

Quality Validation and CSV Manager

The Quality Validation and CSV Manager will lead a team responsible for ensuring all validation activities, including process, cleaning, facility, and computer systems validation, comply with regulatory requirements and GSK quality standards. The role involves managing validation protocols, collaborating with cross-functional teams, and providing technical expertise and training.

GSK Barnard Castle, United Kingdom

On-site Permanent

Associate Director, Global Regulatory Science, CMC

Lead global regulatory CMC strategy and submissions for mRNA-based medicines, ensuring compliance with international regulations. Guide cross-functional teams on regulatory requirements and oversee documentation for biologics across vaccine, oncology, and rare disease programs. Drive process improvements and interact directly with health authorities to support product development.

Moderna London, United Kingdom

Hybrid Permanent

Senior Technician

As a Senior Engineering Technician, you will lead the design, installation, and commissioning of new aseptic manufacturing equipment and facilities. You will work closely with project engineering, quality, and external vendors to ensure systems meet business, regulatory, and GMP requirements, and are ready for operational handover.

GSK Barnard Castle, United Kingdom

On-site Permanent

Senior Project Specialist, Clinical Supplies

This role involves managing clinical supply operations for Moderna’s mRNA-based therapies, ensuring investigational products are labeled, packaged, and distributed efficiently to clinical sites. The specialist will coordinate with vendors, CROs, and internal teams to maintain supply chain compliance and continuity, while supporting digital innovation and process improvements in clinical supply workflows.

Moderna Oxford, United Kingdom

Hybrid Permanent

Director, Data Product Centre of Excellence

This role leads the strategic development and governance of AI-ready data products within a global, regulated environment. The Director will establish enterprise standards, drive adoption across federated teams, and build a scalable operating model for data product delivery. The position emphasizes automation, compliance, interoperability, and measurable value realization across the data lifecycle.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Scientist in Translational Pathology, Oncology

This role involves working in a lab-based GCP environment, supporting translational pathology and biomarker programs. Responsibilities include maintaining quality standards, managing clinical and research specimens, performing laboratory assays, and collaborating with cross-functional teams to ensure laboratory activities align with project needs.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Global Clinical Operations Budget Manager

As a Global Clinical Operations Budget Manager, you will translate complex study assumptions into financial insights, manage budgets and forecasts for clinical trials, and work closely with clinical and finance teams to ensure transparency and accuracy. The role involves partnering across a global matrix environment to drive smarter decisions and optimize trial delivery, ultimately accelerating the development of innovative medicines.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom

Hybrid Permanent

Global Clinical Operations Budget Manager

This role involves managing budgets and financial forecasts for clinical trials, working closely with clinical and finance teams to ensure accuracy and transparency. You will translate complex study assumptions into actionable financial insights, optimize trial delivery, and support process improvements in a global matrix environment.

Novartis London, United Kingdom

Hybrid Permanent

End-to-End Product Lead, AMP

The AMP Product Lead is responsible for defining and executing the vision, strategy, and roadmap for an intelligent content operating system. This role involves collaborating with global stakeholders, managing a team of product owners, and ensuring the product delivers measurable outcomes in productivity, quality, and compliance.

Pfizer United States

On-site Permanent

End-to-End Product Lead, AMP

This role involves leading the development and delivery of an intelligent content operating system called AMP, which connects how marketers plan, create, review, and measure content. The Product Lead will define the product vision, roadmap, and success metrics, manage a team of product owners, and collaborate with stakeholders across content strategy, operations, design, engineering, data, and compliance to ensure alignment and drive measurable outcomes in user productivity, quality, and compliance.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

QA/RA Manager

This role involves leading the design and implementation of regulatory and quality management systems for a portfolio of Class I medical devices, ensuring compliance with ISO 13485 and 21 CFR 820. The candidate will oversee digital EQMS deployment, lead audits, manage post-market surveillance, and build a distributed team while embedding a proactive compliance culture across R&D, supply chain, and commercial functions.

SRG London, United Kingdom

Hybrid Permanent

Quality Engineer (Compliance)

This role involves ensuring medical device and drug-device combination products meet strict regulatory standards throughout development. The Quality Engineer (Compliance) will lead design controls, risk management, and audit readiness activities, working closely with development teams and external partners. Key focus areas include DHF and RMF maintenance, regulatory compliance, and supporting clinical trial investigations.

Next Phase Recruitment Cambridge, Cambridgeshire, United Kingdom

Hybrid Contract

Senior Specialist I, QA Clinical

The Senior Specialist I, QA Clinical is responsible for quality oversight in clinical development, supporting cross-functional relationships and ensuring compliance with GCP/GVP regulations. Key responsibilities include developing and implementing risk-based audit plans, conducting audits, and managing quality events. The role involves working closely with clinical project teams and external stakeholders, and maintaining the quality management system.

Autolus Stevenage, United Kingdom

Hybrid Permanent Flexible

Principal Clinical Project Manager

This role leads complex or pivotal clinical trials from conception to closeout, overseeing cross-functional teams and vendor partnerships. The Principal Clinical Project Manager ensures study delivery within quality, timeline, and budget targets, applying risk-based quality management and driving inspection readiness. They also mentor junior staff and contribute to process improvements within clinical operations.

Autolus London, W12 7RH, United Kingdom

Hybrid Permanent

SERM Scientific Director

The SERM Scientific Director will lead the safety evaluation and risk management of GSK's key assets, ensuring scientifically sound review and interpretation of data. They will develop and execute safety strategies, manage safety governance, and represent GSK on cross-functional teams to address product safety issues and improve regulatory adherence.

GSK

On-site Permanent