34 Quality Assurance And Engineering jobs in London.

Hiring now: Instrument Calibration En @ Perkinelme, Associate Dir Regulatory @ Biomarin, 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, Regulatory Data Admin @ Charlotte , Sr Implementation Consult @ Veeva Syst, Biz Quality Mgr @ Lindus Hea.Explore more at jobswithgpt.com.

🔥 Skills

project management (8) regulatory compliance (8) risk management (6) compliance (4) collaboration (4) Project Management (4) Regulatory Affairs (3) biologics (3) gene therapy (3) CAPA (3)

đź“Ť Locations

London (29) High Wycombe (4) Stevenage (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

Biomarin

Associate Director, Regulatory CMC London
Skills & Focus: Regulatory Affairs, CMC, biologics, pharmaceuticals, gene therapy, global regulatory submissions, documentation, project management, cross-functional teams, drug development
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: Minimum of 10 years of Regulatory Affairs, CMC experience
Type: Hybrid

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

Iqvia

Quality and Compliance Lead (Pharmareview) London
Skills & Focus: Quality Control, Compliance, Pharmaceutical Review, Life Science, Training, Audits, SOPs, Risk Management, Process Improvement, Team Leadership
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
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.

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…

Iqvia

Final Signatory (PharmaReview) London
Skills & Focus: final signatory, pharmaceutical industry, PMCPA/ EFPIA code, MHRA Blue Guide, certification, internal Code training, compliance audits, coaching, mentoring, decision making
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: Minimum 2 years' experience of Final signatory experience. Minimum 5 years experience in Pharmaceutical Industry or equivalent.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

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.

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

Amgen

Supplier Governance Manager London
Skills & Focus: supplier governance, clinical research, biotechnology, project management, process improvement, Good Clinical Practices, FDA regulations, international regulatory guidelines, risk management, collaboration
About the Company: At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are glob…
Experience: Clinical research experience in biopharmaceuticals (biotech, pharma, or CRO)
Type: Flex Commuter / Hybrid
Benefits: Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits.

Veeva Systems

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

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…

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…

Johnson & Johnson

Senior Manager Commercial Quality UK High Wycombe
Skills & Focus: Quality Management System, Market Authorisation, Compliance, Quality Assurance, Risk Management, Quality Planning, Internal Audit, Regulations, Product Quality, Continuous Improvement
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,…
Type: Hybrid
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,…
Director of Regulatory Medical Writing (RegMW) High Wycombe
Skills & Focus: medical writing, regulatory, clinical documents, project management, cross-functional teams, process improvements, mentoring, therapeutic areas, risk management, leadership
About the Company: Johnson & Johnson is a leading global healthcare company dedicated to improving health outcomes for patients through innovative medicines and medical technolog…
Type: Hybrid