Latest Quality Engineer Jobs

Audit Senior Lead (EMEA GMP Audit)

The Audit Senior Lead role involves performing and managing GMP and compliance audits of biopharm, vaccines, and pharmaceutical facilities. Responsibilities include evaluating compliance, managing stakeholder engagement, and producing clear audit reports. The role requires strong communication skills and subject matter expertise in sterile manufacturing.

GSK

On-site Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across EMEA and other highly regulated markets. Responsibilities include evaluating compliance, conducting various types of audits, and producing clear audit reports to inform senior management of identified risks and corrective actions.

GSK

Hybrid Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director at Pfizer will be responsible for developing and maintaining quality plans, ensuring inspection and audit readiness, and providing oversight of process deviations and investigations. This role involves interpreting and applying global regulations, driving compliance, and collaborating with stakeholders to identify and mitigate risks, ensuring the quality and integrity of Pfizer's medicines and vaccines.

Pfizer United Kingdom

On-site Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director will lead the development and maintenance of Quality Plans, ensure inspection and audit readiness, and provide quality oversight of process deviations and investigations. This role involves interpreting and applying regulatory requirements, identifying and mitigating compliance gaps, and driving continuous improvement in pan-regulatory processes and data quality.

Pfizer London, SW7 2AP, United Kingdom

On-site Permanent

Associate Director, Biostatistics (4)

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinicaldevelopment program. The AD provides statistical strategies for the clinical trials and regulatorysubmissions, and is accountable for the statistical deliverables within the program.Lead full scope of...

CSL

Associate Director, Biostatistics

The role involves leading statistical strategy and execution across clinical development programs, including study design, data analysis, and regulatory submissions. The individual will provide expert statistical input, manage internal or outsourced programming teams, and represent biostatistics in interactions with global regulatory agencies. Emphasis is placed on innovation, cross-functional collaboration, and delivery of high-quality statistical outputs for clinical trials and submissions.

CSL

Hybrid Permanent

Head of Make CoE

The Head of Make CoE will lead the transformation of end-to-end manufacturing processes across a global network, partnering with sites and central teams to deliver safer, higher-quality, more sustainable, and more productive operations. Key responsibilities include strategy and roadmap leadership, governance, cross-functional integration, and team development, with a focus on digital and autonomous manufacturing.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Vice President, Head of Clinical Operations

This role involves leading the clinical operations strategy and execution across Recursion’s development portfolio, from study planning to study closeout. You will build and mentor a high-performing team, manage global trials, and ensure operational excellence in an AI-native TechBio company.

Recursion United Kingdom

On-site Permanent

Clinical Scientific Expert (CSE) I

Salary Range:£37,593.50 - £69,816.50Job Description SummaryWork Arrangement: Hybrid Working, #LI-HybridLocation: London (The Westworks), United KingdomRelocation Support: This role is based in London, United Kingdom. Novartis is unable to offer relocation support: please only apply if accessible.ABOUT THE ROLEThe Clinical Scientific...

Novartis London, United Kingdom

Associate Director, Statistical Programming

This role leads statistical programming efforts across global clinical trials, managing teams and driving innovation in data analysis and visualization. The individual will shape programming strategy, ensure audit readiness, and collaborate with cross-functional teams to deliver high-quality statistical outputs. Emphasis is placed on adopting modern tools like R, Shiny, and Git for reproducible, standardized workflows in drug development.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Business Development Manager (South West)

LOCATION: South West RegionJOB TYPE: Full timeHOURS OF WORK: Monday to Friday, 09:00–17:00 (half hour unpaid lunch break)SALARY: £33,000–£36,000 pa + Uncapped Commission (£45,000 pa OTE) + Car + Benefits.JOB PURPOSEYou will strategically manage a territory of customers, maintaining, developing...

Micronclean Skegness, Lincolnshire, United Kingdom £33,000 – £36,000 pa

Pharmaceutical Final Checker

Pharmaceutical Final CheckerITH Pharma specialises in the provision of Parenteral Nutrition, Chemotherapy and CIVAS. Our team provides flexible services with batch and bespoke items for adults, paediatrics and neonates to both NHS and Private Hospitals. The successful candidate will be...

ITH Pharma Middlesex, London, UB8 3QX, United Kingdom £30,073 pa

Senior Development Scientist - Protein Science - London

As a Senior Development Scientist, you will lead the design and optimisation of protein-based assays and workflows, from early feasibility to commercial deployment. You'll apply advanced protein characterisation techniques, mentor a team of scientists, and ensure seamless integration of workflows into the wider platform.

Bond Williams London, United Kingdom

On-site Permanent

Specialist Biomedical Scientist

This role involves managing and developing pathology laboratory services, including analysing specimens, supporting research, and ensuring efficient operations in blood transfusion, haematology, or chemical pathology. The scientist will work closely with consultants and managers, handle sensitive information, and participate in on-call duties with a requirement to live within 30 minutes of the hospital. Rotational shifts including early, late, weekend, and on-call hours are integral to the position.

Spire Healthcare Southampton, Hampshire, SO19 8NJ, United Kingdom

On-site Contract

Senior Production Operator

This role involves producing medical devices in a Grade C cleanroom, following strict SOPs and quality standards. Responsibilities include in-process inspections, maintaining production records, and contributing to process improvements.

THOMAS Professional Mitton, Gloucestershire, GL20 8AW, United Kingdom £32,000 – £38,000 pa

On-site Permanent