Latest Project Services Jobs

Programme Manager (Engineering - Capital Projects)

The Capital Projects’ Programme Manager sits within the Barnard Castle site’s Engineering Projects team. The position provides experienced, visible programme management for the delivery of complex capital programmes and projects within a highly-regulated manufacturing environment. The role liaises with and...

GSK Barnard Castle, United Kingdom

Associate Director, Diagnostic Planning Lead - Oncology

This role leads diagnostic planning initiatives within GSK’s Oncology Translational Medicine team, coordinating cross-functional efforts across clinical development, regulatory, and external partners to advance diagnostic assets. The position ensures alignment of project timelines, manages risks, and supports regulatory submissions, leveraging expertise in biomarkers and in vitro diagnostics within an oncology context.

GSK United States US$151,500 – US$252,500 pa

Hybrid Permanent

Scientist – Peptide Chemistry

This role involves conducting laboratory-based experimental work in peptide chemistry, designing and synthesizing peptides using solid-phase techniques, and contributing to the development of new peptide medicines. The position offers opportunities for personal and professional growth within a dynamic and collaborative team.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Senior Research Scientist – Protein Scientist

The role involves hands-on work in protein biochemistry, including expressing, purifying, and characterizing antibodies and protein constructs. The successful candidate will also perform bioconjugate generation, analytical QC, and collaborate with cross-functional teams to optimize conjugation workflows and evaluate conjugates.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

ViiV Healthcare (GSK) Senior Director, Clinical Development

As a Senior Medical Director at ViiV Healthcare, you will lead the design and delivery of early development plans for HIV treatments, ensuring clinical excellence and medical governance across Phase 1-4 studies. You will collaborate with internal and external stakeholders to design, execute, and interpret clinical studies, focusing on long-acting medicines and ensuring patient safety and data integrity.

GSK United States

On-site Permanent

ViiV Healthcare (GSK) Senior Director, Clinical Development

This role involves leading the design and delivery of early development plans for HIV treatments, ensuring clinical excellence and medical governance across Phase 1-4 studies. You will collaborate with internal and external stakeholders to design, execute, and interpret clinical studies, ensuring patient safety and scientific excellence.

GSK

On-site Permanent

ViiV Healthcare (GSK) Senior Director, Clinical Development

As the Senior Medical Director, you will lead the design and delivery of early development plans for HIV treatments, ensuring clinical excellence and medical governance across Phase 1–4 studies. You will collaborate with internal and external stakeholders to advance ViiV Healthcare's mission of eradicating HIV, focusing on long-acting medicines and novel approaches to treatment and prevention.

GSK

On-site Permanent

MSAT Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product throughout its lifecycle, from development through manufacturing and commercial supply. The Molecule Steward ensures product quality, process robustness, and regulatory compliance by leading technical strategy, coordinating cross-functional teams, and driving continuous improvement across global supply chain sites. The position requires deep scientific expertise, strong leadership in matrixed environments, and active involvement in regulatory submissions and lifecycle management.

GSK €103,500 – €172,500 pa

Hybrid Permanent

MSAT Molecule Steward

This role involves end-to-end technical leadership for a pharmaceutical product across its lifecycle, from development through manufacturing and commercialization. The Molecule Steward ensures product quality, robustness, and compliance by leading technical strategy, process optimization, and cross-functional collaboration across R&D, manufacturing, and regulatory teams. They play a key role in technology transfer, continuous process verification, and maintaining control strategies in a highly regulated environment.

GSK €103,500 – €172,500 pa

Hybrid Permanent

MSAT Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product across its lifecycle, from development through manufacturing and commercialization. The Molecule Steward ensures product quality, regulatory compliance, and process robustness by leading cross-functional teams, defining control strategies, and driving continuous improvement initiatives. It requires deep scientific expertise, strong leadership in matrixed environments, and coordination across R&D, manufacturing, and regulatory functions.

GSK €103,500 – €172,500 pa

Hybrid Permanent

MSAT Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product throughout its lifecycle, from development to commercial manufacturing. The Molecule Steward ensures product quality, robustness, and manufacturability by leading technical strategy, process optimization, and regulatory compliance across global supply chain teams. The position requires deep scientific expertise, cross-functional collaboration, and leadership in resolving complex technical challenges in a regulated environment.

GSK €103,500 – €172,500 pa

Hybrid Permanent

Principal Medical Writer

This role involves authoring and delivering high-quality clinical regulatory documents, leading cross-functional teams, and managing complex writing projects. The Principal Medical Writer will interpret clinical and statistical data, ensure compliance with regulatory requirements, and contribute to global regulatory submissions.

GSK Stevenage, United Kingdom

Hybrid Permanent

Principal Medical Writer

The Principal Medical Writer will author and deliver high-quality clinical regulatory documents, lead cross-functional teams in developing clinical dossier documents for global regulatory submissions, and manage complex writing projects. They will interpret complex clinical and statistical information, ensuring compliance with GSK standards and regulatory requirements.

GSK

Hybrid Permanent

Engineering Technician (12 month secondment)

This role involves providing hands-on engineering support within a sterile pharmaceutical manufacturing environment, focusing on maintenance, compliance, and continuous improvement of production systems. The technician will work across complex equipment and processes, ensuring GMP standards, managing SAP systems, and supporting projects such as new product introductions. Key responsibilities include breakdown repairs, PPM activities, calibration, and supervision of contractors in a regulated, shift-based operation.

GSK Barnard Castle, United Kingdom

On-site Temporary

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategies. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.

GSK Stevenage, United Kingdom

Hybrid Permanent