Biotechnology Jobs in Woking

Software Engineer (Data Services), London

This role involves working in a fast-paced, interdisciplinary team to build a cutting-edge ML-based software platform for drug discovery. Responsibilities include data engineering, service-oriented architecture, and collaboration with scientists and ML researchers to accelerate scientific breakthroughs.

Isomorphic Labs London, United Kingdom

On-site Permanent

Associate Director, Medical Affairs

This role involves shaping and executing medical strategy for immunology products across their post-launch lifecycle, with a focus on scientific engagement, evidence generation, and collaboration with key opinion leaders and internal teams. The position supports global medical and scientific communication, contributes to clinical understanding, and aligns with commercial and research partners. Based in Maidenhead or Zurich, it operates in a hybrid model with three days onsite weekly.

CSL

Hybrid Permanent

Associate Director, Medical Affairs

This role involves shaping medical strategy for immunology products, supporting post-launch lifecycle management, and driving scientific engagement with key opinion leaders and patient groups. The individual will coordinate investigator-led studies, provide scientific input to commercial teams, and support evidence generation across global markets. Collaboration with cross-functional teams and affiliates is central to advancing clinical understanding and therapeutic impact.

CSL United Kingdom

Hybrid Permanent

Director, Portfolio Development Process & Standards Lead

This role leads the establishment and maintenance of processes and standards across CSL's global Portfolio Development function, ensuring high-quality clinical trial planning, evaluation, and reporting. The Director will drive process improvement, SOP governance, training curriculum development, and cross-functional change initiatives within a dynamic biotech R&D environment. They will work closely with leadership and international teams to reduce complexity, improve quality and speed, and align procedural frameworks across clinical development, biomarkers, and commercial operations.

CSL

Hybrid Permanent

GLP/GCLP Vendor Oversight and QA Lead (EU)

This role involves leading the quality oversight of external partners in R&D and regulated activities, managing the vendor lifecycle from due diligence to continuous improvement, and ensuring compliance with GLP/GCP/GMP/GVP standards. The position requires close collaboration with various departments to maintain high-quality standards and regulatory compliance.

CSL United Kingdom

On-site Permanent

Senior Clinical Trial Case Manager

This role involves leading cross-functional teams in reviewing safety data, mentoring junior staff, and ensuring compliance with GxP guidelines and international regulations. The position also focuses on managing pharmacovigilance procedures, conducting impact assessments of new legislation, and supporting regulatory inspections and audits.

CSL

On-site Permanent

Junior Data Scientist - NLP/text mining

Your new companyYou'll be joining a global biopharmaceutical organisation supporting scientific information, intelligence, and data-driven decision-making across research and development as part of a highly experienced team with plenty of learning and training opportunities.The company has a highly collaborative environment...

Hays Life Sciences London, United Kingdom £175 – £275 pd

Trainee Administrator

Trainee AdministratorJoin Cellular Pathology Services (CPS) in Watford as a Trainee Administrator and start building your career within a supportive and innovative healthcare environment.If you’ve also worked in the following roles, we’d also like to hear from you:Administration Assistant, Administrative...

Cellular Pathology Services Holywell, Hertfordshire, WD18 6PG, United Kingdom £24,784 pa

Head of Marketing

Head of MarketingLocation: West SussexSalary: Up to £70,000, Plus BenefitsDrive the marketing function for a respected manufacturer supplying global organisations. This is a hands‑on Head of Marketing role ideal for a commercially minded marketer who enjoys both strategy and execution.About...

OM Search Consultants LTD Haywards Heath, West Sussex, United Kingdom £60,000 – £70,000 pa

Workshop Engineer (Electronics)

This role involves diagnosing, repairing, and calibrating medical devices at component level within a workshop environment. The engineer will troubleshoot electrical faults, follow technical drawings, and maintain accurate service records. The position is part of a team focused on ensuring the reliability and performance of critical medical equipment.

FIELD Southcote, Berkshire, RG1 6AF, United Kingdom £28,000 – £33,000 pa

On-site Permanent

Lead Genomic Data Scientist - Cancer (we have office locations in Cambridge, Leeds & London)

Leads cancer genome analysis and interpretation projects within a research environment, providing technical and scientific leadership. Manages a high-performing team and drives end-to-end genomic analysis, from design to delivery, in collaboration with internal and external stakeholders. Focuses on improving best practices in genome analysis and benchmarking tools for whole genome data processing.

Genomics England Canary Wharf, London, E14 5AB, United Kingdom £71,000 – £100,000 pa

Hybrid Permanent

Submission Readiness Document Manager

This role involves managing the submission-readiness of clinical documents to ensure they meet regulatory and quality standards for global submissions. The professional will oversee technical editing, support compliance with health authority guidelines, and work closely with cross-functional teams to improve document processes. It requires expertise in clinical documentation systems and a strong focus on operational excellence in a fast-paced, regulated environment.

Novartis London, United Kingdom £49,140 – £91,260 pa

Hybrid Permanent

Director, CMC Regulatory Affairs

Lead the development and execution of global CMC regulatory strategies for small molecule drugs in clinical trials and marketing applications. Author and manage high-quality regulatory submissions across the US, EU, and rest of world, while advising cross-functional teams on compliance, risk mitigation, and evolving GMP standards. Collaborate closely with internal and external stakeholders to ensure timely delivery of regulatory deliverables and support clinical development programs.

Recursion London, W1C 2QP, United Kingdom

Remote Permanent

Senior Regulatory Affairs Specialist

This role involves leading regulatory strategy and compliance for medicinal products, medical devices, and cosmetics across the UK and Ireland. The specialist will manage submissions, support product launches, ensure adherence to post-Brexit regulations, and maintain compliance through interactions with MHRA and HPRA. It requires strong expertise in regulatory documentation, lifecycle management, and cross-functional collaboration within a dermatology-focused pharmaceutical environment.

GI Group Euston, London, NW1 2EA, United Kingdom £75,000 pa

Hybrid Contract