Biotechnology Jobs in Bolton

Head of Operational Excellence

The Head of Operational Excellence leads process improvement activities and staff, aligning projects with business strategies. They establish and maintain performance metrics, manage operational processes, and oversee training and development of subject matter experts in a regulated, global matrix organization.

CSL United Kingdom

Associate Director, Biostatistics

The Associate Director, Biostatistics, leads statistical contributions to clinical development programs, including study design, data analysis, and regulatory submissions. They collaborate with cross-functional teams, manage outsourcing, and ensure the quality and timeliness of deliverables.

CSL £212,000 – £251,000 pa

Hybrid Permanent

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

GLP/GCLP Vendor Oversight and QA Lead (EU)

This role focuses on end-to-end quality oversight of external vendors and suppliers involved in regulated R&D activities, ensuring compliance with GLP, GCP, GMP, and GVP standards. The individual will lead vendor qualification, audit management, quality agreement negotiation, and continuous performance monitoring, while collaborating with cross-functional teams including Clinical, CMC, Safety, and Legal. A key aspect is driving compliance, data integrity (ALCOA+), and continuous improvement across third-party partners through risk-based assessments, CAPA follow-up, and QMS integration.

CSL United Kingdom

On-site Permanent

Senior Clinical Trial Case Manager

This role involves leading safety data review and pharmacovigilance activities within clinical trials, ensuring compliance with international regulations such as GxP. The individual will mentor team members, manage CAPAs, support regulatory inspections, and contribute to safety reporting and risk management. Key responsibilities include MedDRA coding, safety data analysis, and developing pharmacovigilance procedures to support global regulatory requirements.

CSL

On-site Permanent