Biotechnology Jobs in Bolton

Process Leader (First Line Manager) – Sterile Production

This role involves leading a team of operators in a fast-paced, highly regulated sterile manufacturing environment. Responsibilities include managing daily operations, ensuring compliance with cGMP standards, and driving continuous improvement through Lean principles and digital technologies.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent Shift-work

Associate Director Clinical Supply IRT

This role involves leading the onboarding and continuous improvement of IRT standards and studies for AstraZeneca's clinical trials. Responsibilities include technical documentation, risk assessment, test script development, training, and process optimization. The position requires deep knowledge of R&D supply chain, clinical development processes, and IRT systems, with a focus on delivering high-quality, efficient clinical trial supplies.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

QA/ Validation Supervisor, Pharmaceutical

This role involves leading a small QA team, ensuring compliance with regulatory standards, and overseeing quality systems and validation activities. Responsibilities include report writing, managing QA documentation, participating in audits, and driving continuous improvement initiatives.

NMS Recruit Ltd t/a Russell Taylor Group Worsley, Manchester, M28 2GE, United Kingdom £40,000 – £45,000 pa

On-site Permanent

QA Officer, Pharmaceutical

The QA Officer will work in a biotech company, focusing on generating and reviewing SOPs, handling customer complaints, and maintaining GMP compliance. They will also participate in quality improvement initiatives, manage documentation, and support regulatory audits.

NMS Recruit Ltd t/a Russell Taylor Group Alderley Edge, Cheshire, SK10 4UB, United Kingdom £28,000 – £34,000 pa

Senior Clinical Application Specialist - MCS

This role involves driving the adoption of advanced clinical applications in microsurgery and tumour workflows, working closely with surgeons, clinical teams, and hospital decision-makers. The Specialist will support technology integration, engage key stakeholders, and contribute to strategic business development and revenue growth.

Manpower Manchester, United Kingdom

Hybrid Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, including medical monitoring, safety data review, and clinical data management. The position also includes mentoring others and contributing to protocol design and study strategy.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Scientific Programme Manager, Clinical Genomics

The Scientific Programme Manager will play a crucial role in international genomics quality assurance, ensuring diagnostic laboratories worldwide produce accurate and reliable genetic test results. Responsibilities include managing EQA schemes, interpreting complex genomic data, and collaborating with senior scientific leaders and stakeholders to maintain high standards and improve diagnostic genomics practices.

MFK Recruitment Salford, Manchester, M41 8PH, United Kingdom £50,169 pa

Hybrid Permanent

Principal Scientific Programme Manager, Clinical Genomics

The Principal Scientific Programme Manager will lead and support the delivery of specialist External Quality Assessment (EQA) schemes in clinical genomics. This role involves managing timelines, quality, and programme performance, as well as supporting the design and development of new EQA schemes. The position requires strong scientific knowledge, experience in genomics and quality assurance, and the ability to communicate effectively with senior stakeholders.

MFK Recruitment Salford, Manchester, M41 8PH, United Kingdom £59,157 pa

Hybrid Permanent