Biotechnology Jobs

• London
• Hybrid
• Lead · manages people

Serves as the clinical trial pharmacy subject matter expert across global oncology programmes, advising on investigational product handling, preparation, storage and accountability, and on hazardous drug and CSTD requirements. Develops pharmacy manuals and training for site pharmacists and study teams, supports audits and CAPAs, and oversees FSP pharmacists and external vendors. Hybrid role spanning London, Paris or Cambridge MA.

Closed System Transfer Devices

• London
• Hybrid
• Mid-level

Leads global cross-functional teams to plan, coordinate and deliver regulatory submissions for new marketing authorisations, new indications and other major filings. Manages integrated submission timelines, scenario planning, risk mitigation and forecasts, working with Regulatory Affairs, Clinical, Quality and Manufacturing under the CTD/eCTD framework.

RIMS

• New York, United States
• Hybrid · 2–3 days in office
• US$124,400 – US$207,400 pa
• Lead · manages people

Leads the strategy, design and lifecycle management of Pfizer's clinical supply chain systems, aligning a 3-5 year product roadmap with Global Clinical Supply objectives. Partners with digital product managers and business SMEs on solution design, process improvement and portfolio prioritisation, reporting metrics to senior leadership. Hybrid role with up to 15% travel.

• Haywards Heath
• Hybrid · 3 days in office
• Director · manages people

Leads a global team of development and regulatory project managers overseeing complex R&D programs across a therapeutic area, including new product development and lifecycle management. Acts as strategic partner to TA and R&D leadership, driving portfolio planning, agile delivery, risk removal and cross-functional alignment as part of the Portfolio & Operations Excellence leadership team.

Microsoft Project · Planview · Smartsheet +1

• Maidenhead
• Lead · manages people

Provides medical and scientific expertise on clinical safety across the full product lifecycle, with emphasis on evaluating safety data during clinical development and post-approval. Chairs the Safety Management Team, oversees signal detection, aggregate reports (DSURs, PSURs, RMPs) and regulatory responses, and sets safety strategy for global cross-functional development and post-marketing teams.

DSUR · PSUR · RMP +2

• London
• Hybrid

Provides technical leadership for structuring, connecting and reusing product and process data across digital products and manufacturing systems, with a focus on the digital product profile. Builds and maintains CI/CD pipelines, integrations and environments spanning R&D, CMC and commercial platforms, applying ontologies, knowledge graphs and AI-assisted engineering under GxP and Responsible AI controls.

PDLM · MES · LES/LIMS +5

• Stevenage
• Hybrid · 2 days in office
• US$242,250 – US$403,750 pa
• Director

Accountable for end-to-end clinical development of a multi-tumor oncology asset, from first-in-human through registrational trials, regulatory approval and initial market launch. Acts as senior clinical representative at governance forums and leads cross-functional, matrixed teams spanning research, precision medicine, medical affairs and commercial. Requires deep antibody-drug conjugate and global health authority experience.

AI/ML

• Macclesfield
• On-site
• Senior
• Permanent

Designs and executes work plans for early drug discovery projects within a Protein Sciences team, supporting multiple projects and presenting results to clients. Hands-on role focused on recombinant protein expression using insect cell systems such as BEVS, S2 and Sf9, including construct design, baculovirus generation and troubleshooting difficult targets like membrane proteins.

BEVS · Sf9 · Sf21 +2

• Leeds
• Director · manages people

Executive leadership role owning QA and regulatory compliance for the Clinical Pharmacology Services unit, covering CPU operations, GMP pharmacy activities and Phase IB/IIA early-phase trials. Sets risk-based quality strategy, inspection readiness and audit programs, leads global matrixed QA teams and represents the company externally on GCP/GMP matters.

• Uxbridge
• Director · manages people

Owns the clinical strategy for one or more neuropsychiatry programs, serving as Clinical Trial Physician and clinical point of accountability for the Clinical Development Team. Leads trial design, data interpretation, regulatory submissions and health authority interactions, with matrix leadership across global scientific teams.

• Cambridge
• Hybrid · 3 days in office
• Director

Lead digital health strategy engagements with AstraZeneca R&D, top pharma and biotechs, shaping operating models and roadmaps across clinical development. Directs project teams on AI and digital solutions such as ePRO/eCOA, wearables and digital biomarkers, building business cases and tracking value realisation. Combines consulting, protocol design support and scaled implementation in a matrixed environment.

ePRO · eCOA · Wearables +1

• Cambridge
• Senior

Introduction to role:The Senior Scientist – Upstream Process Development position is a temporary maternity-cover role responsible for the hands-on scientific and technical delivery of upstream mammalian cell culture process development activities supporting AstraZeneca’s biologics pipeline. Working under minimal supervision, the…

• Saffron Walden
• Hybrid
• £4,395 pm
• Senior · manages people
• Contract

Lead solution architecture for digital experience initiatives spanning web applications, APIs, content platforms and AI-enabled services. Remain hands-on through discovery, prototyping and architectural development while providing technical direction, mentoring and people management to the development team. Bridges UX and engineering, shaping LLM, retrieval-augmented generation and agentic patterns into accessible, sustainable services.

React · Angular · Drupal +7

• Uxbridge
• Hybrid

Provides scientific and clinical expertise for a cardiovascular therapy area, driving UK medical strategy, research plans and field tactical activities alongside the Field Medical Manager. Manages publications, supports Health Technology Assessment work and acts as a nominated medical signatory, with around 15% national and international travel.

• Macclesfield
• On-site
• Senior · manages people
• Permanent

Acts as the key analytical point of contact for clients, leading the transfer of commercial analytical methods across multiple laboratory sites and ensuring their robustness, performance and compliance for drug substances. Coordinates analytical activities, supports change programmes and market access projects, and leads a small team of scientists while working with Quality, Regulatory and Manufacturing. Based at a pharmaceutical client facility in Macclesfield.