42 Quality Engineering jobs in London.

Hiring now: Instrument Calibration En @ Perkinelme, Aggregate Report Sr Scien @ Biogen, Sr Quality Mgr @ Charlotte , Quality And Compliance Le @ Iqvia, Cmc Regulatory Affairs Pr @ Perrigo, Quality Compliance Sr Mgr @ Amgen, Sr Software Engr Focused @ Mytos, Associate Dir Packaging T @ Jazz Pharm, Sr Implementation Consult @ Veeva Syst, Biz Quality Mgr @ Lindus Hea.Explore more at jobswithgpt.com.

🔥 Skills

project management (9) regulatory compliance (9) compliance (6) Regulatory Affairs (6) Project Management (6) collaboration (5) Pharmaceutical (4) risk management (4) pharmaceutical (4) cross-functional team (4)

đź“Ť Locations

London (32) High Wycombe (4) Hatfield (2) Stevenage (1) Maidenhead (1) Guildford (1) Bishops Stortford (1)
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Perkinelmer

Instrument & Calibration Engineer Stevenage
Skills & Focus: Calibration, Laboratory Instrumentation, Metrology, GxP Experience, Pharmaceutical, Science, Engineering, ISO Calibration, UKAS, Original Equipment Manufacturers

Biogen

Aggregate Report Senior Scientist Maidenhead
Skills & Focus: aggregate reports, PSURs, DSURs, PADERs, pharmacovigilance, safety queries, medical safety, scientific safety, process improvement, global safety compliance

Charlotte Tilbury Beauty

Senior Quality Manager London
Skills & Focus: Quality Management, Cosmetics, ISO 22716, ISO 9001, Product Development, Quality Standards, Manufacturing Processes, Compliance, Root Cause Analysis, Statistical Analysis
About the Company: Founded by British makeup artist and beauty entrepreneur Charlotte Tilbury MBE in 2013, Charlotte Tilbury Beauty has revolutionised the face of the global beau…
Experience: Extensive experience in Quality and/or Manufacturing management in the cosmetic industry.
Type: Full-time
Benefits: 25 days holiday (plus bank holidays) with an additional day to celebrate your birthday, inclusive parental leave policy…

Iqvia

Quality and Compliance Lead (PharmaReview) London
Skills & Focus: Quality compliance, pharmaceutical review, subject matter expert, training development, internal compliance, external regulations, quality control, audits, CAPA, risk evaluation
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 3-5 years relevant experience in pharmaceutical review and/or compliance
Type: Full-time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.
Quality and Compliance Manager (Pharmareview) London
Skills & Focus: compliance, quality, policy, training, audit, risk management, collaboration, GCP, life sciences, pharmaceutical
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 3-5 years relevant experience in pharmaceutical review (AQP / Sig) and / or compliance
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Perrigo

CMC Regulatory Affairs Project Manager London
Skills & Focus: CMC Regulatory Affairs, project management, healthcare products, medical devices, cosmetics, regulatory strategies, product development, quality management, technical documentation, compliance
About the Company: We are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the …
Experience: Minimum of 7 years of relevant work experience, preferably in CMC Regulatory Affairs or R&D.
Benefits: Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career dev…

Amgen

Quality Compliance Senior Manager - Inspections (GCP) London
Skills & Focus: Quality Management, Quality Assurance, Regulatory Inspections, Good Clinical Practices, Risk Assessment, Clinical Trials, Compliance Risks, Quality Metrics, Regulatory Agency, CAPA
About the Company: Amgen is one of the world's leading biotechnology companies aimed at serving patients through the research, manufacturing, and delivery of biotechnology produc…
Experience: Experience in Quality Management, Quality Assurance in the pharmaceutical/biotech industry.
Type: Flex Commuter / Hybrid
Benefits: Vast opportunities for learning and career advancement, generous total rewards plan, and a diverse community of belongi…

Mytos

Senior Software Engineer focused on Platform & Security London
Skills & Focus: Senior Software Engineer, Platform, Security, infrastructure, GMP environments, SOC 2 Type 2, cell therapy manufacturing, compliance posture, secure solutions, regulatory compliance
About the Company: Mytos focuses on automating human cell production, a crucial process in biotech for drug discovery and development. They aim to impact the development of cures…
Experience: Senior level experience in software engineering, particularly in security and compliance.
Type: Full-time
Senior Software Engineer focused on Platform & Security London
Skills & Focus: Senior Software Engineer, Platform, Security, infrastructure, GMP environments, SOC 2 Type 2, cell therapy manufacturing, compliance posture, secure solutions, regulatory compliance
About the Company: Mytos focuses on automating human cell production, a crucial process in biotech for drug discovery and development. They aim to impact the development of cures…
Experience: Senior level experience in software engineering, particularly in security and compliance.
Type: Full-time
Senior Software Engineer focused on Platform & Security London
Skills & Focus: Senior Software Engineer, Platform, Security, infrastructure, GMP environments, SOC 2 Type 2, cell therapy manufacturing, compliance posture, secure solutions, regulatory compliance
About the Company: Mytos focuses on automating human cell production, a crucial process in biotech for drug discovery and development. They aim to impact the development of cures…
Experience: Senior level experience in software engineering, particularly in security and compliance.
Type: Full-time

Jazz Pharmaceuticals

Associate Director, Packaging Technology London
Skills & Focus: packaging technology, pharmaceutical, pack design, project management, regulatory compliance, cross functional teams, stakeholder management, quality system, serialization, engineering
About the Company: Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to deve…
Experience: minimum of 10 years’ experience in the field
Type: Full-time

Charlotte Tilbury Beauty

Regulatory Data Administrator London
Skills & Focus: data management, regulatory product data, accuracy, reporting, collaborative, product development, supply chain, Syndigo, formulations, ingredients
About the Company: Founded by British makeup artist and beauty entrepreneur Charlotte Tilbury MBE in 2013, Charlotte Tilbury Beauty has revolutionised the face of the global beau…
Benefits: 25 days holiday (plus bank holidays) with an additional day to celebrate your birthday, inclusive parental leave policy…

Veeva Systems

Senior Implementation Consultant – Pharmacovigilance / Safety Systems London
Skills & Focus: implementation, pharmacovigilance, SaaS, life sciences, project management, drug safety, consulting, configuration, requirements gathering, customer training
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Experience: At least 5 years of working experience in the life sciences industry with the majority spent in Drug Safety, Pharmacovigilance, Healthcare, or adjacent Safety Industry
Type: Full-time
Benefits: Employees receive an amount equivalent to 1% of their base salary annually to support non-profit(s) of their choice.

Jazz Pharmaceuticals

Senior Pharmacovigilance Study Operations Lead London
Skills & Focus: Pharmacovigilance, Safety Assessment, Adverse Event, Data Management, Regulatory Compliance, Vendor Oversight, Process Improvement, Case Processing, Training, Collaboration
About the Company: Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to deve…
Type: Full-time

Lindus Health

Business Quality Manager London
Skills & Focus: ISO certification, ISO27001, ISO9001, eQMS, supplier assessments, internal audits, compliance, continuous improvement, quality indicators, clinical trials
About the Company: Our mission is to fix clinical trial infrastructure using software to help innovative companies run faster, more reliable, and patient-friendly clinical trials…
Experience: Experience in ISO certification processes, conducting supplier assessments, and working with an eQMS.
Salary: Competitive salary, plus stock options
Type: Full-time
Benefits: Competitive salary, stock options, unlimited holidays, flexible working, health & wellbeing cashback scheme, Gympass me…
Business Quality Manager London
Skills & Focus: ISO certification, ISO27001, ISO9001, eQMS, supplier assessments, internal audits, compliance, continuous improvement, quality indicators, clinical trials
About the Company: Our mission is to fix clinical trial infrastructure using software to help innovative companies run faster, more reliable, and patient-friendly clinical trials…
Experience: Experience in ISO certification processes, conducting supplier assessments, and working with an eQMS.
Salary: Competitive salary, plus stock options
Type: Full-time
Benefits: Competitive salary, stock options, unlimited holidays, flexible working, health & wellbeing cashback scheme, Gympass me…

Novartis

Associate Director, Clinical QA London
Skills & Focus: Quality oversight, clinical trials, Good Clinical Practice, quality risk management, stakeholder collaboration, quality incident management, audits, inspections, CAPA, continuous improvement
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare profess…
Type: Hybrid Working

Parexel

Regulatory Affairs Manager - CMC biologics London
Skills & Focus: Regulatory Affairs, CMC, Biologics, Pharmaceuticals, Submission Strategies, Quality Control, Risk Management, Project Management, Technical Documentation, Collaboration
About the Company: Parexel is a global biopharmaceutical services company that helps clients navigate the complex and ever-changing regulatory landscape.
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote/Office-based

Veeva Systems

Product Expert - Regulatory Information Management (RIM) London
Skills & Focus: Regulatory Operations, Regulatory Affairs, RIM products, customer success, submissions, eCTD, submission planning, product management, stakeholder resources, industry regulations
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Experience: life science industry experience in Regulatory Operations or Regulatory Affairs
Type: Full-time
Benefits: flexibility to work from home or in the office
Implementation Consultant – Pharmacovigilance / Safety Systems London
Skills & Focus: Pharmacovigilance, Safety Systems, Vault Safety, implementation, consultant, SaaS, Life Sciences, project management, collaboration, configuration
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Experience: At least 3+ years of experience in Life Sciences, Healthcare, or an adjacent Safety industry
Benefits: 1% Veeva Giving program, work wherever is best for you, commitment to fostering a culture of inclusion and diversity.

Comind

Senior QARA Engineer - Software London
Skills & Focus: QA/RA, medical devices, regulatory compliance, ISO 13485, IEC 62304, FDA 21 CFR Part 820, EU MDR, software validation, risk management, cybersecurity
About the Company: At CoMind, we are developing a non-invasive neuromonitoring technology that will result in a new era of clinical brain monitoring.
Experience: Demonstrable experience in QA/RA for software in medical devices or a related field
Type: Full time
Benefits: Company equity plan, Company pension scheme, Private medical, dental and vision insurance, Group life assurance, Compre…

Cai

Project (CQV) Engineer London
Skills & Focus: Commissioning, Qualification, Validation, CQV Procedures, Safety, Life Sciences, SOPs, Installation Qualification, Operational Qualification, Project Management
About the Company: CAI is a 100% employee-owned company established in 1996, that has grown year over year to nearly 850+ people worldwide. We provide commissioning, qualificatio…
Experience: 5+ years in CQV SME roles for life sciences
Type: Full-time
Benefits: Hands-on certifications and professional training; a collaborative culture that invests in employee future.
Project (CQV) Engineer London
Skills & Focus: Commissioning, Qualification, Validation, CQV Procedures, Safety, Life Sciences, SOPs, Installation Qualification, Operational Qualification, Project Management
About the Company: CAI is a 100% employee-owned company established in 1996, that has grown year over year to nearly 850+ people worldwide. We provide commissioning, qualificatio…
Experience: 5+ years in CQV SME roles for life sciences
Type: Full-time
Benefits: Hands-on certifications and professional training; a collaborative culture that invests in employee future.

Orchard Therapeutics

Regulatory CMC Specialist London
Skills & Focus: Regulatory CMC, gene therapy, biologics, Advanced Therapy Medicinal Products (ATMPs), life cycle management, health authority submissions, Module 3/QOS, investigational products, cross-functional team, stakeholder collaboration
About the Company: Orchard Therapeutics is a global biotechnology gene therapy company dedicated to transforming the lives of people affected by rare diseases through the develop…
Experience: Minimum 3 years of regulatory CMC experience with biologics and/or Advanced Therapy Medicinal Products (ATMPs). Experience in Gene Therapy Medicinal products is a plus.
Type: Full-time
Regulatory CMC Specialist London
Skills & Focus: Regulatory CMC, gene therapy, biologics, Advanced Therapy Medicinal Products (ATMPs), life cycle management, health authority submissions, Module 3/QOS, investigational products, cross-functional team, stakeholder collaboration
About the Company: Orchard Therapeutics is a global biotechnology gene therapy company dedicated to transforming the lives of people affected by rare diseases through the develop…
Experience: Minimum 3 years of regulatory CMC experience with biologics and/or Advanced Therapy Medicinal Products (ATMPs). Experience in Gene Therapy Medicinal products is a plus.
Type: Full-time

Orchard

CMC Lead London
Skills & Focus: CMC strategy, cross-functional team, risk register, product profiles, regulatory submissions, GMP compliance, drug development, stakeholder management, project management, cell & gene therapies
Experience: Substantial Biotech/Pharmaceutical industry experience including demonstrated experience leading a multidisciplinary CMC team in a matrix setting
CMC Lead London
Skills & Focus: CMC strategy, cross-functional team, risk register, product profiles, regulatory submissions, GMP compliance, drug development, stakeholder management, project management, cell & gene therapies
Experience: Substantial Biotech/Pharmaceutical industry experience including demonstrated experience leading a multidisciplinary CMC team in a matrix setting

Playstation

Senior Director, Product Safety and Compliance London
Skills & Focus: product safety, regulatory compliance, global regulatory standards, electronics manufacturing, risk management, team management, leadership, collaboration, analytical skills, professional certifications
About the Company: PlayStation isn’t just the Best Place to Play — it’s also the Best Place to Work. Today, we’re recognized as a global leader in entertainment producing The Pla…
Experience: 15+ years of experience in product safety and compliance within the electronics manufacturing industry, with at least 5 years in a senior leadership role.
Benefits: Discretionary bonus opportunity, Hybrid Working (within Flexmodes), Private Medical Insurance, Dental Scheme, 25 days h…

Perrigo

Regulatory Affairs - Senior Associate London
Skills & Focus: Regulatory Affairs, OTC medicines, product development, regulatory documentation, compliance, MAA submissions, trackers, eCTD publishing, communication, problem-solving
About the Company: At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 pl…
Experience: Minimum of 3 years in Regulatory Affairs, specifically with OTC medicines.
Type: Full-time
Benefits: Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career dev…

Jazz Pharmaceuticals

Mgr, Pharmaceutical Development Quality Assurance London
Skills & Focus: Quality Assurance, GMP, cGMP, Investigational Medicinal Products, Clinical Trials, Pharmaceuticals, Quality Systems, Regulatory Submissions, Auditing, Product Development
About the Company: Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to deve…
Experience: Experience working in finished product pharmaceuticals, including analytical chemistry, quality assurance, quality control, development, and/or manufacturing areas.
Benefits: medical, dental and vision insurance, retirement savings plan, and flexible paid vacation.

Sgs

Medical Device Auditor London
Skills & Focus: MDSAP, audit, regulatory compliance, technical approval, service delivery, query corrections, KPI, medical device, certificates, risk management
About the Company: SGS is the world's leading inspection, verification, testing, and certification company.

Playstation

Senior Product Safety and Compliance Manager London
Skills & Focus: regulatory compliance, safety, certification, product launches, compliance procedures, project management, interpersonal skills, hardware product development, problem-solving, training
About the Company: PlayStation isn’t just the Best Place to Play — it’s also the Best Place to Work. Today, we’re recognized as a global leader in entertainment producing The Pla…
Experience: 8+ years
Type: Hybrid

Perrigo

Regulatory Affairs Associate London
Skills & Focus: Regulatory Affairs, Medicinal Products, Compliance, Product License Variations, EU Legislation, Quality, Submissions, Documentation Preparation, Regulatory Intelligence, Team Collaboration
About the Company: Perrigo is a top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over-the-counter and infant formula.
Experience: Minimum one year experience in a Regulatory environment
Benefits: Competitive compensation and benefits tailored to support employees and their families, along with career development o…

Veeva Systems

Product Expert - Regulatory Information Management London
Skills & Focus: Regulatory Operations, Regulatory Affairs, Regulatory Information Management, Customer Success, Product Management, Submissions, eCTD, Submission Archive, Product Roadmap, Stakeholder Engagement
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Experience: life science industry experience in Regulatory Operations or Regulatory Affairs
Type: Full-time
Benefits: Work Anywhere flexibly, supporting both remote work and office work environments.

Johnson & Johnson

Manager, Immunology Regulatory Medical Writing High Wycombe
Skills & Focus: Immunology, Regulatory, Medical Writing, Clinical Documents, Project Management, Cross-Functional, Team Leadership, Process Improvement, Pharmaceutical, Communications
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: At least 8 years of relevant pharmaceutical/scientific experience; at least 6 years of relevant medical writing experience.
Type: Full-time
Analyst II, Regulatory Medical Writing High Wycombe
Skills & Focus: Regulatory, Medical Writing, Pharmaceutical, Clinical Documents, Protocols, Clinical Study Reports, Team Environment, Writing, Quality Control, Project Management
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: At least 2 years of relevant pharmaceutical/scientific experience is required.
Type: Full-time
Benefits: We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority,…
Associate Director, Global Labeling Product Leader High Wycombe
Skills & Focus: Regulatory Affairs, Labeling, Pharmaceutical, Documentation, Compliance, Project Management, Scientific Communication, Continuous Improvement, Global Labeling Strategy, Team Leadership
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: 8 years of professional work experience required, with 6 years of direct regulatory labeling content experience.
Type: Hybrid

Viatris Uk Healthcare

Regulatory Affairs Executive Hatfield
Skills & Focus: regulatory activities, post-approval submissions, regulatory compliance, strategic assessment, health authority requirements, documentation, quality systems, stakeholder alignment, project management, team collaboration
About the Company: Viatris empowers people worldwide to live healthier at every stage of life by providing access to high quality trusted medicines and advancing sustainable oper…
Experience: Applied technical UK Regulatory Affairs experience, creating high-quality documentation and submissions.
Benefits: Competitive compensation package, hybrid work model, health & wellness programmes, life cover, excellent employer-match…

Viatris

Director Global CMC Strategy Hatfield
Skills & Focus: regulatory, CMC strategy, eyecare products, submissions, quality, stakeholders, regulatory affairs, collaboration, pharmaceutical, leadership
About the Company: At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolv…
Experience: Extensive pharmaceutical experience with relevant technical experience (Quality, Technical Services, R&D) and pharmaceutical regulatory experience required.
Benefits: Excellent career progression opportunities, work-life balance initiatives, bonus scheme, health insurance, pension.

Ergomed

Executive Director, PV Strategy Guildford
Skills & Focus: pharmacovigilance, regulations, EU/UK QPPV, PV processes, audits, gap analysis, consultancy services, training, drug safety, client-facing reports

Steris Corporation

Senior Electrical Engineer Bishops Stortford
Skills & Focus: Electrical, Control, Instrumentation, System design, Product Development, Testing, Regulatory documentation, Continuous improvement, Electromechanical, Medical Electrical Standards
About the Company: STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention.
Experience: 5+ years experience required.
Type: Onsite