Latest Genetic Engineering Jobs

Senior, Forward Deployed / Full Stack Engineer (Document Authoring & Knowledge Systems)

Embedded forward deployed engineer role in GSK's Enterprise AI team, working within the Chemical Manufacturing & Control area to prototype AI solutions at days-to-weeks cadence. Focuses on document authoring and generation for regulatory filings, agentic workflows, RAG, knowledge systems and LLM evaluation, with heavy daily use of AI coding agents. Proven prototypes are handed off to a Sr. Solutions Engineer for scale-up.

GSK London

Hybrid

Senior, Forward Deployed / Full Stack Engineer (Document Authoring & Knowledge Systems)

Embedded with CMC business teams, you take high-priority AI use cases from problem framing to working prototypes at days-to-weeks cadence, then ship first production versions. The work centres on document authoring and generation for regulatory filings, building agentic and RAG pipelines, human-in-the-loop review workflows, and LLM evaluation with golden datasets and regression testing.

GSK Stevenage

Hybrid

(Fixed Term) Manufacturing Associate I

Operate manufacturing equipment for mRNA vaccine production under cGMP and SOPs, maintaining documentation, gowning and housekeeping standards. Partner with Quality Assurance on batch disposition, lead root cause analysis and CAPA for deviations, and troubleshoot equipment and digital system issues. Work 100% onsite with digital and Generative AI-enabled manufacturing technologies.

Moderna Oxford

On-site Temporary

(Fixed Term) Laboratory Technician, Clinical Biomarker Laboratory, Immunoassay

Support assay development, qualification, validation and clinical sample testing within Moderna's Immunoassay group, generating bioanalytical data that informs clinical trials. Work is primarily lab-based (≥85% of time) under a study lead, with responsibility for data integrity, reagent preparation, equipment upkeep and compliance with GCP/ISO standards.

Moderna Oxford

On-site Temporary Clearance Required

Associate Director (Scientific Data and Publications)

Oversees GSK R&D's enterprise portfolio of external scientific content and data licenses, managing budget, forecasting, cost controls and vendor commercial terms. Acts as senior interface to major information providers and connector across scientific, procurement, legal, copyright and technology teams, ensuring copyright-compliant use. Positions the portfolio for AI and text-mining exploitation, shaping future licensing needs.

GSK USA - Pennsylvania - Upper Providence

Analytical Network Strategy Senior Director

Leads the development and execution of the analytical (QC testing) network strategy across GSK's global supply chain, translating approved strategy into an operational roadmap and securing endorsement from governance forums such as the Supply Chain Review Board. Drives benchmarking, KPI and reporting frameworks, and capability building across GSC Strategy, with focus on large molecules, ADCs and Oligos.

GSK Stevenage

Associate Director, Pipeline Project Management for BD

Provides R&D project management for Business Development transactions, from early diligence through governance, deal execution and integration into business as usual. Acts as a strategic partner to BD, Alliance Management and R&D stakeholders, leading cross-functional planning, risk management and governance readiness across multiple therapeutic areas and development phases.

GSK Grimsby US$139,425 – US$232,375 pa

Senior Manager, Risk & Compliance Business Partners R&D

Leads a team of risk and compliance business partners supporting GSK's R&D technology, covering clinical, discovery and regulatory systems. Combines hands-on cyber risk consulting and assurance with team leadership, owning the risk register, GxP/SOX compliance, audit readiness and stakeholder engagement across Ware and London sites.

GSK London

Hybrid

Director, Oncology Translational Medicine, Clinical Biomarkers

Leads the design and execution of clinical biomarker and translational medicine strategies for late-stage oncology assets, defining patient segmentation and decision criteria within Clinical Matrix Teams. Validates predictive, pharmacodynamic and resistance biomarkers using platforms such as NGS, ctDNA, flow cytometry and multi-omic analyses to inform dose selection and go/no-go decisions.

GSK USA - Pennsylvania - Upper Providence US$189,750 – US$316,250 pa

Hybrid

Director, Oncology Translational Medicine, Clinical Biomarkers

Leads the design and execution of clinical biomarker and translational medicine strategies for late-stage oncology assets, defining patient segmentation and decision criteria within Clinical Matrix Teams. Oversees biomarker assay development, sample testing plans and data packages across platforms such as NGS, IHC, flow cytometry and ctDNA, working with internal and external partners.

GSK London US$189,750 – US$316,250 pa

Hybrid

SERM Medical Director

Provides medical and scientific leadership for pharmacovigilance and risk management of oncology assets in clinical development, interpreting safety data, detecting signals and delivering benefit-risk recommendations. Represents Safety on cross-functional matrix teams and governance committees, and interacts with regulators. Hybrid role based in the UK.

GSK Siena, Italy €81,750 – €136,250 pa

Hybrid

SERM Medical Director

Provides medical and scientific leadership for pharmacovigilance and risk management of oncology assets in clinical development, interpreting safety data, detecting and escalating signals, and delivering benefit-risk recommendations. Represents Safety on cross-functional matrix teams and governance committees, and interacts with regulators and external experts. Hybrid role based in the UK with a global matrix environment.

GSK Warsaw, Poland

Hybrid Permanent

Associate Medical Director, Safety Evaluation and Risk Management (SERM)

Provides medical and scientific expertise in safety evaluation and risk management for GSK assets across clinical development and post-marketing settings. Leads signal detection, regulatory periodic reports, and benefit-risk assessments while collaborating with cross-functional teams including Clinical Operations, Regulatory, and Biostatistics. Involves presenting complex safety issues to senior governance committees and contributing to global regulatory submissions.

GSK Durham €87,000 – €145,000 pa

Hybrid

Associate Medical Director, Safety Evaluation and Risk Management (SERM)

Provides medical and scientific expertise in safety evaluation and risk management for GSK assets across clinical development and post-marketing settings. Leads signal detection, benefit-risk assessment, regulatory periodic reports and RMPs, working within a global cross-functional matrix alongside Clinical Operations, Regulatory and Biostatistics. Distinct for its strong focus on pharmacovigilance governance, safety strategy and scientific writing.

GSK Greater Poland €87,000 – €145,000 pa

Hybrid Permanent

Associate Medical Director, Safety Evaluation and Risk Management (SERM)

Provides medical and scientific expertise in safety evaluation and risk management for GSK assets across clinical development and post-marketing settings. Leads signal detection, periodic regulatory reports, RMPs and benefit-risk assessments within a global cross-functional matrix, presenting complex safety issues to senior governance committees. Distinct for its blend of pharmacovigilance strategy, regulatory writing and matrix leadership.

GSK London €87,000 – €145,000 pa

Hybrid Permanent