Biotechnology Jobs in Preston

Case Management Intake Manager

Oversees the vendor responsible for logging and triaging global adverse event reports in CSL's pharmacovigilance system, ensuring accurate, timely, and compliant case intake. Develops guidance, provides training, and maintains audit readiness for regulatory compliance. Acts as subject matter expert on intake processes across cross-functional projects and procedural documentation.

CSL United Kingdom

Director, Search & Evaluation Early TA Lead (CVR)

This role leads the identification, evaluation, and advancement of early-stage external innovation opportunities in the Cardiovascular/Renal therapeutic area. The individual will shape sourcing strategies, co-lead cross-functional assessment of new product opportunities, and drive due diligence and transaction execution in collaboration with Business Development. Embedded in the Therapeutic Area Leadership Team, the position plays a strategic role in portfolio development and external engagement with biotech, academia, and investors.

CSL

Hybrid Permanent

Director, Search & Evaluation Early TA Lead (CVR)

Leads strategic sourcing and evaluation of early-stage (preclinical to Phase 1) external innovation opportunities in the Cardiovascular/Renal therapeutic area. Drives due diligence, shapes partnering strategies, and collaborates with Business Development to execute transactions. Embedded in the Therapeutic Area Leadership Team to align external innovation with portfolio planning.

CSL

Director, Search & Evaluation Early TA Lead (Haem)

Leads strategic sourcing and evaluation of early-stage innovation in haematology, from preclinical to Phase 1 assets. Drives due diligence, shapes partnering strategies, and executes transactions in collaboration with Business Development. Embedded in the Therapeutic Area Leadership Team to influence portfolio planning and external innovation priorities.

CSL

Director, Search & Evaluation Early TA Lead (Haem)

Leads external innovation sourcing and evaluation in Haematology, identifying preclinical to Phase 1 assets, driving due diligence, and shaping early partnering strategies. Works within the Therapeutic Area Leadership Team to advance high-potential opportunities and collaborates with Business Development to execute deals. Engages with biotech, academia, and investors to build a robust pipeline.

CSL

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

Head of Quality, Pharmaceutical

Lead the quality function in a GMP-regulated pharmaceutical manufacturing environment, overseeing QA, QC, and compliance systems. Drive quality strategy, regulatory readiness, and continuous improvement across operations. Manage audits, inspections, and a high-performing team within a growing organisation.

NMS Recruit Ltd t/a Russell Taylor Group Boothstown, Manchester, M28 1LT, United Kingdom £60,000 – £65,000 pa

On-site Permanent

Business Development Manager - Life Science

Drive new business in contamination control for life science and cleanroom manufacturing environments across the North of England. Focus on consultative, solution-led sales, building strategic relationships with key decision-makers and delivering tailored contamination control strategies. Transition successful wins into long-term partnerships within a regulated, technical environment.

Progress Sales Recruitment Manchester, United Kingdom £55,000 – £65,000 pa

Technical Service Engineer

This role involves providing on-site and remote technical support for advanced robotics systems used in pharmaceutical and biotech environments. The engineer will perform preventative maintenance, diagnose and resolve technical issues, manage spare parts forecasting, and act as a customer-facing subject matter expert. The position includes 24/7 on-call responsibilities and extensive training on proprietary systems, with a strong focus on customer satisfaction and cross-functional collaboration.

Wallace Hind Selection Oldham, Manchester, United Kingdom £52,000 – £56,000 pa

Technical Service Engineer

This role involves providing on-site and remote technical support for advanced robotics systems used in pharmaceutical and biotech environments. The engineer will perform preventative maintenance, diagnose issues, manage spare parts forecasting, and act as a subject matter expert for customers. With extensive training provided, the position emphasizes customer collaboration, problem-solving, and use of D365 and service reporting tools across a dynamic field-based workload.

Wallace Hind Selection Manchester, United Kingdom £52,000 – £56,000 pa

On-site Permanent

Head of Quality / Senior Quality Manager - Pharmaceutical

This role involves leading the entire Quality function (QA and QC) within a pharmaceutical manufacturing site, overseeing a team of 15 and ensuring strict adherence to GMP and regulatory standards. The individual will drive the site's Quality strategy, manage audits and inspections (including MHRA and customer audits), and lead continuous improvement initiatives across quality systems, validation, and compliance. With a strong emphasis on leadership and team development, the role sits at the heart of the site’s leadership team and requires strategic oversight alongside hands-on operational involvement.

Radar Recruitment Manchester, United Kingdom £60,000 pa

Head of Quality - Pharmaceuticals

Leads quality assurance and control functions within a pharmaceutical manufacturing and import environment, ensuring compliance with EU GMP standards. Responsible for maintaining inspection-readiness, managing regulatory audits, and serving as the primary liaison with the MHRA. Develops and drives the site's Quality Management System as a member of the Site Leadership Team.

Smart4Sciences Manchester, United Kingdom £60,000 – £65,000 pa

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

This role involves providing medical and scientific leadership in safety evaluation and risk management for GSK's clinical and post-marketing assets. The Associate Medical Director will lead signal detection, contribute to pharmacovigilance strategy, and ensure robust safety oversight across global development programs. Working within a cross-functional matrix, the role emphasizes evidence-based decision-making, regulatory compliance, and proactive risk communication to protect patient safety.

GSK Manchester, M4 6AL, United Kingdom €87,000 – €145,000 pa

Hybrid Permanent