Biotechnology Jobs in Bolton

Associate Director, Safety Epidemiology – Global Patient Safety

Lead the design and execution of post-authorisation safety studies using real-world data to assess and communicate the safety profiles of AstraZeneca’s medicines. Provide strategic epidemiological input to regulatory submissions, safety signal evaluations, and diversity initiatives, collaborating with internal teams and external partners. Drive methodological excellence in pharmacoepidemiology and contribute to global patient safety decision-making across a broad product portfolio.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

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

Biologics Account Manager

This role involves driving clinical demand for respiratory biologics by building strategic relationships with healthcare professionals and multi-disciplinary teams across a defined UK territory. The Account Manager will lead formulary access, support homecare utilization, and collaborate with cross-functional teams to implement account plans in complex secondary care environments. Success requires strong commercial acumen, stakeholder influence, and deep understanding of the NHS commissioning landscape.

AstraZeneca Sheffield, United Kingdom

On-site 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

Associate Process Leader (Trainee Manager) – Sterile Production

This role involves supporting sterile manufacturing operations within a cGMP environment, focusing on production planning, compliance, and continuous improvement. The candidate will gain experience in deviation management, root-cause analysis, and cross-functional collaboration with Quality, Engineering, and Operations teams. Emphasis is placed on developing leadership skills and contributing to a culture of safety, efficiency, and manufacturing excellence.

AstraZeneca Macclesfield, United Kingdom

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

Head of Quality, Pharmaceutical

Leads the Quality function in a GMP-regulated pharmaceutical manufacturing environment, overseeing QA, QC, QMS, and regulatory compliance. Responsible for driving quality strategy, leading audits, managing CAPA and change controls, and developing a high-performing team. Focuses on continuous improvement and operational excellence within a growing organisation.

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

Director, Generative AI – Chemical Development

Leads the strategy and implementation of Generative AI and agentic workflows in chemical development to accelerate CMC processes and scientific decision-making. Drives adoption of AI in regulated environments, focusing on use cases like knowledge mining, report generation, and experiment planning. Works across scientific, compliance, and digital teams to embed responsible, scalable AI into routine workflows.

AstraZeneca Macclesfield, United Kingdom

Biomedical Scientist

About UsPure Healthcare are the UK’s leading healthcare recruitment agency, committed to delivering service excellence. We have many years of framework healthcare recruitment experience. We have built up a wide network of contacts, clients and resources within our business to...

Pure Healthcare Blackburn, Lancashire, BB1 7DP, United Kingdom £26 ph

Bank Biomedical Scientist

Bank Biomedical Scientist/Spire Manchester / 0 HoursSpire Manchester Hospital has an exciting opportunity for a Biomedical Scientist to join the team on a Bank 0-hour contract.Duties and responsibilities:To assist in the organisation, management and development of services within specialty of...

Spire Healthcare Manchester, United Kingdom

Quality & Regulatory Associate

This role involves supporting the development and maintenance of a Quality Management System aligned with ISO13485 and FDA requirements in a growing med-tech company. The candidate will manage regulatory documentation, design controls, and quality processes, contributing to audit readiness and continuous improvement. It's a hands-on position with direct impact on product compliance and regulatory submissions.

Taylorollinson Manchester, United Kingdom £35,000 – £45,000 pa

Hybrid Permanent