Latest Innovation Jobs

Sr. Data Platform Engineer - Computer System Validator

As a Senior Data Platform Engineer, you will build, scale, and operate a validated data platform with petabyte-scale data, ensuring data integrity and traceability in a GxP-compliant environment. You will collaborate with biologists, chemists, and data scientists to make Recursion’s vast datasets discoverable and queryable, supporting the company’s mission to advance drug discovery through technology and biology.

Recursion United Kingdom US$142,500 – US$220,500 pa

Hybrid Permanent

Technical Program Manager, ClinTech Strategy & Analytics

This role involves project managing and tracking the ClinTech roadmap, working closely with Clinical Development Operations and Decision Science to translate priorities into actionable plans. You will also support the communication of ClinTech’s progress to senior leadership and external audiences, contributing to vendor assessments and build-vs-buy evaluations. The role is at the heart of a high-visibility team building a platform to accelerate drug development.

Recursion North Tyneside, NE29 8EP, United Kingdom £136,200 – £211,100 pa

Hybrid Permanent

Research Associate - Biology Automation

This role involves developing and running automated biochemical and cell-based assays to support drug discovery projects. You will work on a leading-edge automation platform, ensuring high-quality data and collaborating with cross-functional teams to drive small molecule therapeutics development.

Recursion Crathes, Alba / Scotland, United Kingdom

On-site Permanent

Business Insights Manager or Secondment)

The Business Insights Manager will analyze data from various sources, including sales and market activity, to develop actionable recommendations that support AstraZeneca’s strategic goals. Key responsibilities include leading market research projects, forecasting, and collaborating with teams in Marketing, Finance, and Market Access, specifically focusing on the Cardio-Renal therapy area.

AstraZeneca London, United Kingdom

Hybrid Contract

Regulatory Conformance Officer (12-month / Secondment)

As a Regulatory Conformance Officer, you will ensure that GSK's products meet all licensing and regulatory requirements, maintaining compliance with global market authorisations and supporting regulatory submissions. You will collaborate with multiple functions, including manufacturing, R&D, and global regulatory affairs, to deliver regulatory strategies and inspection readiness.

GSK Barnard Castle, United Kingdom

On-site Contract

Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL

Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL

SLDC Coordinator (Site Launch and Data Control) - 12-month / Secondment

This role involves managing the creation and changes of packaging for new and existing products within GSK’s supply chain, using systems like SAP, GLAMS, and CHAMPS. The coordinator ensures compliance with GMP and EHS standards while working across functions such as Quality, Regulatory, Procurement, and Logistics to maintain supply security. The position supports new product launches and pack amendments, drives process improvements, and maintains data integrity across site master records.

GSK Barnard Castle, United Kingdom

On-site Contract

Senior Engineering Technician /Secondment

This role involves providing hands-on engineering leadership to support the introduction and scale-up of new pharmaceutical products within a regulated manufacturing environment. The technician will ensure equipment and processes meet safety, compliance, and reliability standards, lead technical issue resolution, and coordinate engineering activities across teams during product launches and validation. Emphasis is placed on operational readiness, change control, and continuous improvement in a GMP-compliant setting.

GSK Barnard Castle, United Kingdom

On-site Contract

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of clinical trials for GSK's oncology portfolio, focusing on hematological malignancies. Key responsibilities include collaborating with multidisciplinary teams, ensuring patient safety, and contributing to regulatory submissions and publications.

GSK Stevenage, United Kingdom

Hybrid Permanent

Head, PV and Regulatory QA

TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...

CSL

Head, PV and Regulatory QA

TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...

CSL

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, Diagnostic Planning Lead - Oncology

Leads diagnostic planning activities within oncology translational medicine, coordinating cross-functional teams and external partners to advance diagnostic development programs. Oversees project timelines, regulatory documentation, budget management, and strategic alignment, with a focus on biomarker technologies and IVD development in support of oncology assets.

GSK Stevenage, United Kingdom US$151,500 – US$252,500 pa

Hybrid Permanent

Associate Director, Diagnostic Planning Lead - Oncology

This role involves leading diagnostic planning for oncology projects within GSK’s Translational Medicine team, coordinating cross-functional activities across clinical development, regulatory, and external partners. The Associate Director will manage timelines, budgets, and deliverables for diagnostic development programs, ensuring alignment with biomarker strategies and regulatory requirements. The position plays a key strategic role in advancing oncology assets through integrated project management and collaboration with diagnostics manufacturers and internal stakeholders.

GSK London, United Kingdom US$151,500 – US$252,500 pa

Hybrid Permanent