Biotechnology Jobs in Blackpool

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Associate Director, R&D Project Management

Leads the operational delivery of high-impact, global R&D projects within a cross-functional biotech environment. Focuses on strategic planning, budget and timeline management, risk mitigation, and stakeholder reporting. Provides mentorship to junior project management staff and ensures robust project execution across drug research, development, and manufacturing.

CSL

Hybrid Permanent

(Fixed Term) Manufacturing Associate I

Operate and maintain mRNA vaccine production equipment in compliance with cGMP and safety standards, executing manufacturing processes, troubleshooting equipment and digital systems, and supporting quality documentation and continuous improvement initiatives. Work within a cross-functional team to ensure timely batch release and operational excellence in a fast-paced, highly regulated environment.

Moderna Oxford, United Kingdom

On-site Temporary

(Fixed Term) Manufacturing Associate I

Operate production equipment for mRNA vaccine manufacturing in compliance with cGMP and safety standards. Perform routine maintenance, support deviation investigations, and contribute to continuous improvement in a highly regulated, technology-driven environment. Work collaboratively with QA and cross-functional teams to ensure timely batch disposition and operational excellence.

Moderna

On-site Temporary

Associate Director, Clinical Trial Disclosure & Transparency

This role leads global clinical trial disclosure and transparency strategy, ensuring compliance with international regulations such as FDAAA 801, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while managing redaction of confidential information for public release. They act as a key liaison with regulatory bodies and internal teams, driving process efficiency and vendor performance across the clinical development lifecycle.

CSL

Senior Clinical Trial Case Manager

Manages clinical trial case management activities, ensuring compliance with international and national regulations including GxP and pharmacovigilance standards. Oversees safety reporting, vendor performance, and case processing for serious adverse events, while acting as a key liaison for inspections and audits. Provides training, supports database enhancements, and ensures accurate coding and consistency in safety data analysis.

CSL

Vaccines Safety Sciences Lead

Leads and manages pharmacovigilance safety sciences functions, ensuring compliance with global regulatory standards and overseeing signal detection, safety data analysis, and process optimization. Provides strategic direction for evolving PV legislation and acts as a subject matter expert in audits and inspections. Supports drug development and post-marketing safety reporting while driving data visualization and analytical improvements.

CSL

Hybrid Permanent

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