Biotechnology Jobs

• Liverpool
• Director · manages people

Leads the Operational Excellence function at a major influenza vaccine manufacturing site, deploying Lean, Six Sigma and the CSL Operating System to translate strategy into operational priorities and financial benefits. Owns the site management system, structured problem solving and continuous improvement, coaching senior leaders and leading the OE team. Reports to the Manufacturing Site Lead and sits on the Site Leadership Team.

CSL Operating System

• London
• Hybrid
• £67,900 – £126,100 pa
• Senior

Co-leads cross-functional Clinical Trial Teams and global studies from planning through close-out, managing timelines, budgets, risks and inspection readiness. Partners across global and local functions on recruitment, data operations and vendor performance, while championing operational excellence and continuous improvement.

• Oxford
• On-site
• Mid-level
• Temporary

Hands-on individual contributor role operating production equipment for mRNA vaccine manufacturing at the Harwell site, following cGMP, SOPs and safety requirements. Involves troubleshooting equipment and digital issues, basic maintenance, documentation with Quality Assurance, and RCA/CAPA investigations, with exposure to continuous improvement and Generative AI tools.

Generative AI

• Livingston
• Entry level

Performs and documents analytical procedures in a regulated laboratory, running routine data analysis and checking results against tolerances. Prepares data for LIMS upload, supports quality investigations and deviations, and calibrates and maintains lab equipment. Also trains other lab personnel and escalates unusual results to senior staff.

LIMS

• Livingston
• On-site
• Entry level

Assembles clinical trial test kits with specimen collection materials according to protocol, prepares investigator instruction manuals and flowcharts, and packages completed kits with documentation and ancillary supplies for shipment. Monitors inventory levels and alerts supervisors when supplies run low to prevent study delays. Site-based role requiring strong attention to detail and organizational skills.

• Oxford
• On-site
• Entry level
• Temporary

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.

Generative AI

• 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.

• Hyderabad, India
• On-site
• Director · manages people

Acts as the primary interface between business stakeholders, biostatisticians, statistical programmers and technical delivery teams, translating clinical and statistical requirements into scalable R-based analytics, automation workflows and enterprise reporting. Leads requirement workshops, manages a small team, and oversees releases with end-to-end traceability, regulatory compliance and audit readiness across the clinical trial lifecycle.

• Oxford
• On-site
• Mid-level
• Contract

Design, roll out and maintain an ISO 9001-aligned Quality Management System across a research institute, covering document control, audit programmes and management reviews. The role also involves delivering QMS training and acting as a trusted advisor to programme leaders, on a 12-month fixed term contract.

• London
• Hybrid
• Lead · manages people

Senior operational lead for GSK's Global Supply Chain Digital & Technology function, acting as trusted advisor to the SVP. Owns strategic planning, portfolio governance, PMO orchestration, business operations, workforce planning, change leadership and communications, using AI and automation to drive simplification across a complex global matrix.

AI · Automation

• London
• Hybrid
• Senior

Leads global clinical data transparency and disclosure across registries and regulatory platforms such as CTIS, EMA Policy 0070 and Health Canada PRCI, acting as subject matter expert for assigned therapeutic areas. Manages vendor partnerships, FOI access requests, redaction and lay summary work, plus SOP governance, compliance reporting and audit readiness within Global Regulatory Affairs Excellence.

CTIS · ClinicalTrials.gov · EU Clinical Trial Register +3

• 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

• London
• Hybrid · 3 days in office
• Director · manages people

Lead all externalised drug discovery and preclinical lab operations, building and scaling a global CRO infrastructure for an AI-first drug design platform. Oversee experimental throughput, data QC and turnaround times, embed data-generation-by-design standards, and manage vendor governance, budgets and a team of CRO Scientific Leads, Operations Managers and Compound Managers.

AlphaFold · Agentic AI

• London
• Hybrid · 3 days in office
• Senior

Operating Partner supporting VPs of AI on high-priority strategic initiatives, acting as a trusted advisor and operational force-multiplier. The role involves translating complex machine learning concepts into executive communications, driving cross-functional alignment without line authority, and unblocking inefficiencies across research, engineering, product and operations in a fast-scaling environment.

AlphaFold

• London
• Remote
• Senior

Responsible for the successful delivery of clinical studies at assigned investigator sites, acting as the primary point of contact for site management, monitoring, and study execution. Leads site preparation, initiation, routine monitoring, and close-out, conducting onsite and remote visits, source data review and verification, and CRF review while managing risk-based quality and regulatory compliance. Works within a local study team supporting a key sponsor, with travel across the UK and internationally.

CTMS · eTMF