Last updated 2026-07-04
70 QA Engineering Jobs in London, ENG, United Kingdom
Browse 70 QA Engineering jobs across London, ENG, United Kingdom. Listings are updated hourly and include salary data where available.
Market data for QA Engineering jobs in London, ENG, United Kingdom
Professionals focused on ensuring product quality, compliance, and process improvement across various engineering and manufacturing sectors.
Companies with current QA Engineering listings
| Company | Active jobs |
|---|---|
| Johnson & Johnson Services, Inc. | 5 |
| AbbVie | 3 |
| Fortrea | 3 |
| Galderma Limited (UK) | 3 |
| Moderna Biotech Manufacturing UK Ltd | 3 |
| 1207 Merck Sharp & Dohme (UK) Ltd. | 2 |
| Boston Scientific | 2 |
QA Engineering jobs by schedule
QA Engineering jobs by seniority
Common QA Engineering job titles
QA Engineering jobs by listed location
| Location | Active jobs | Share |
|---|---|---|
| London, ENG, United Kingdom | 39 | 66% |
| Maidenhead, ENG, United Kingdom | 8 | 14% |
| Stevenage, ENG, United Kingdom | 5 | 8% |
| High Wycombe, ENG, United Kingdom | 4 | 7% |
| Slough, ENG, United Kingdom | 3 | 5% |
FAQ
- How many QA Engineering jobs are listed in London, ENG, United Kingdom?
- This page currently shows 70 QA Engineering jobs in London, ENG, United Kingdom.
- Which companies are hiring for QA Engineering roles in London, ENG, United Kingdom?
- Current listings include roles from Johnson & Johnson Services, Inc. (5 jobs, 7%), AbbVie (3 jobs, 4%), Fortrea (3 jobs, 4%), Galderma Limited (UK) (3 jobs, 4%), and Moderna Biotech Manufacturing UK Ltd (3 jobs, 4%).
- What seniority levels are common for QA Engineering jobs in London, ENG, United Kingdom?
- The visible seniority mix includes Senior (32 jobs, 46%), Mid (30 jobs, 43%), and Entry (8 jobs, 11%).
- What work schedules are common for QA Engineering jobs in London, ENG, United Kingdom?
- The visible schedule mix includes Full time (69 jobs, 99%) and Contract (1 job, 1%).
- What QA Engineering job titles are common in London, ENG, United Kingdom?
- Common titles include Clinical Research Associate (4 jobs, 6%), Manager of Clinical Trial Managers II (2 jobs, 3%), QA Senior Manager (2 jobs, 3%), Qualified Person (QP) / Senior Quality Assurance Manager (2 jobs, 3%), and Quality & Compliance Manager (2 jobs, 3%).
- What does this market snapshot include?
- Most visible listings are full-time (69 of 70). Senior-level roles account for 32 of 70 listings. 2 of 70 visible postings include structured pay data.
Related jobs
Snapshot updated 4hr, 6m ago
0603 Seqirus UK Limited
Jul 3- This role serves as a GVP Auditor within our Research & Development Quality audit program, responsible for executing the global…
- Professional Experience: Quality Assurance experience within a GVP-regulated environment, demonstrating a strong understanding of drug safe…
Orchard Therapeutics
Jul 1- This position may also provide support to the Regulatory Science team managing submissions for development programs, and/or to the Regulato…
- Key Elements and Responsibilities Under the guidance of the Senior Director, Regulatory Science, the successful candidate will support the…
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Galderma Limited (UK)
Jul 1- Clinical or biomedical background relevant to drug development preferred.
- Work closely with Medical Experts, Biostatisticians, Clinical Operations, Safety, Regulatory Affairs, and other stakeholders to ensure inte…
More roles at Galderma Limited (UK)
Kent Careers
Jun 30- Job Description About the job: Kent is seeking a Procurement Quality Control Supervisor to lead and support procurement quality activities,…
- Procurement Quality Oversight Review procurement documents to ensure quality requirements are accurately reflected in Material Requisitions…
Pae
Jun 30- Strong understanding of QA/QC across engineering, procurement, manufacturing, construction, and commissioning.
- Ensure supplier and contractor compliance with quality requirements, CQAPs, ITPs, LTQRs, and contractual standards.
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Medisafe UK Limited
Jun 30- We are currently recruiting for Senior Quality Engineer vacancy.
- Required Experience Min 5 years working experience of ISO13485 or similar Min 5 years working in manufacturing Data analysis experience…
Clinical Research Associate - Scotland
- Partner with internal teams (country operations, finance, regulatory affairs, pharmacovigilance, legal, regional operations, HQ) and extern…
- Perform site management and monitoring activities in compliance with ICH-GCP, Sponsor SOPs, local laws/regulations, protocol, site monitori…
More roles at 1207 Merck Sharp & Dohme (UK) Ltd.
MSD
Jun 29- Partner with internal teams (country operations, finance, regulatory affairs, pharmacovigilance, legal, regional operations, HQ) and extern…
- Perform site management and monitoring activities in compliance with ICH-GCP, Sponsor SOPs, local laws/regulations, protocol, site monitori…
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MHRA
Jun 26- To support the contract management, performance and delivery of the BP publication and laboratory services suppliers.
- Experience of working in a pharmaceutical quality environment or equivalent.
Qureight Ltd
Jun 26- Requirements What we need: Minimum of 1-2 year(s) of clinical trial site management experience is desirable but not essential Demonstrated…
- Track and report project and site milestones and maintain relevant internal systems with project specific information.
More roles at Qureight Ltd
TFS HealthScience
Jun 25- Who We're Looking to Connect With Experienced Clinical Quality professionals embedded within clinical operations Strong GCP consultants who…
- Typical Qualifications Solid experience in Clinical Quality Assurance, clinical operations, or a related function In-depth knowledge of GCP…
1006 United Kingdom
Jun 25- The role works cross‑functionally and across sites to support timely, consistent, and compliant execution of NC/CAPA remediation actions Ke…
- This role focuses on supporting compliance with applicable Quality System requirements, including FDA 21 CFR Part 820, ISO 13485:2016, MDSA…
Associate Director, Clinical Risk Management
- Participates in Clinical risk Management, cross R&D quality, cross functional and cross sector working groups to develop or refine processe…
- Maintains CQP (Clinical Quality Plans) in quality repository to facilitate regular progress reviews of quality support services in addition…
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Catalent
Jun 25- The Role: Perform analytical testing including (but not limited to): Routine particle size analysis (laser diffraction) Cleaning verificati…
- In this role, you will perform analytical testing on a variety of samples in alignment with defined methods, SOPs, and…
QA Senior Manager
- Demonstrated experience with quality systems, CAPA management, root cause analysis, issue management, escalation handling, and/or process i…
- Job Overview: Leads global process quality oversight activities by monitoring, trending, and evaluating escalations, quality events, audit/…
Fortrea
Jun 24- QA Senior Manager Job Overview: Leads global process quality oversight activities by monitoring, trending, and evaluating escalations, qual…
- Demonstrated experience with quality systems, CAPA management, root cause analysis, issue management, escalation handling, and/or process i…
More roles at Fortrea
Boston Scientific
Jun 23- Serve as a subject matter expert in Quality Systems, ensuring compliance with applicable regulatory standards such as ISO 13485, EU…
- About the role: The Principal Quality Specialist serves as a senior Quality leader supporting large-scale, complex initiatives within the M…
More roles at Boston Scientific
Thermo Fisher Scientific
Jun 23- Essential Functions: Co-ordinate and support the testing and documentation of all aspect of characterisation, qualification and stability,…
- This role ensures compliance with Good Manufacturing Practices (GMP), regulatory requirements, and internal standards, supporting the quali…
More roles at Thermo Fisher Scientific
Leonardo UK Ltd
Jun 23- Working knowledge of quality tools like Root Cause Corrective Action (RCCA), Process Mapping, Verification, Pattern Fault Lifecycle, and Fi…
- Support continuous improvement initiatives across production, engineering, and quality workflows.
More roles at Leonardo UK Ltd
Quality & Compliance Manager
- Be the specialist on quality management with oversight of quality critical management topics, risk issues and performance data utilising co…
- Plan and deliver an internal audit programme to assess compliance with standards and company policies; lead/support external audits, ensuri…
More roles at Vanderlande Industries United Kingdom Ltd
Cencora
Jun 22- Key Responsibilities will include: Support the European Quality Manager in the effective operation, maintenance and continuous improvement…
- Support the management of supplier and contract service provider Quality Agreements , including coordination of documentation, review cycle…
Associate Director, Global Regulatory Science, CMC
- This pivotal role involves leading regulatory activities, developing CMC strategies for international submissions, ensuring compliance, and…
- Enhance regulatory processes and procedures supporting CMC components.
More roles at Moderna Biotech Manufacturing UK Ltd
CoMind
Jun 19- Design, write, and execute test protocols for hardware, software, and system-level design verification testing Develop and qualify test met…
- As a Verification Test Engineer, you will own the design and execution of V&V test activities for CoMind’s device, working…
More roles at CoMind
Amgen
Jun 18- Contribute to cross-functional initiatives and special projects that enhance supplier governance and operational effectiveness.
- You will partner with suppliers and cross-functional stakeholders to optimize performance, mitigate risks, drive continuous improvement, an…
Mytos
Jun 18- The Role: We are looking for a high-growth principal PD/MSAT Scientist to join our Biology team and push the limits…
- Subject matter expertise in cell therapy development and manufacture across the PD → MSAT → cGMP pipeline.
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