Last updated: 2025-05-22

27 Quality Engineering jobs in London.

Hiring now: Instrument Calibration En @ Perkinelme, Sr Quality Mgr @ Charlotte , Vp Of Regulatory @ Flo Health, Prod Expert Regulatory In @ Veeva Syst, Sr Qara Engr Software @ Comind, Proj Cqv Engr @ Cai, Regulatory Cmc Spec @ Orchard Th, Mgr Global Supply Plannin @ Orchard, Regulatory Ops Document M @ Shionogi, Cmc Regulatory Affairs Pr @ Perrigo.Explore more at at kaamvaam.com

šŸ”„ Skills

project management (5) regulatory compliance (4) cross-functional team (4) compliance (4) pharmacovigilance (4) audits (4) Regulatory Affairs (3) eCTD (3) medical devices (3) Project Management (3)

šŸ“ Locations

London (20) Guildford (4) High Wycombe (2) Stevenage (1)
šŸ” Go to full job search

Perkinelmer

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

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 beauā€¦
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 policyā€¦

Flo Health

VP of Regulatory London
Skills & Focus: regulatory strategy, medical device regulations, FDA, EU MDR, SaMD, ISO 13485, digital health, regulatory submission, QMS, medical device certification
About the Company: Flo is the worldā€™s #1 health app on a mission to build a better future for female health, offering digital health solutions with AI-powered, privacy-first, cliā€¦
Experience: Over 10 years of regulatory affairs experience in the medical device domain
Benefits: Competitive salary, professional growth opportunities, flexible working options, health and wellbeing perks

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 theā€¦
Experience: life science industry experience in Regulatory Operations or Regulatory Affairs
Type: Full-time
Benefits: flexibility to work from home or in the office

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, Compreā€¦

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, qualificatioā€¦
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, qualificatioā€¦
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 developā€¦
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 developā€¦
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

Manager, Global Supply Planning London
Skills & Focus: supply planning, demand planning, drug products, manufacturing planning, KPI improvements, biotechnology, external manufacturing, GMP, cell therapy, supply chain systems
About the Company: Orchard is a global leader in cell and gene therapies, focusing on innovative manufacturing and supply chain solutions for the biotechnology and pharmaceuticalā€¦
Experience: At least 7 years of end-to-end supply chain experience with a minimum of 3 years in the biotechnology or pharmaceutical industry.
Type: Full-time
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

Shionogi

Regulatory Operations Document Manager London
Skills & Focus: Document Manager, pharmaceutical, eCTD, compliance, regulatory documentation, document management systems, Word formatting, PDF remediation, submission-ready, time management
About the Company: Shionogi is a leading pharmaceutical company dedicated to improving the health and well-being of people around the world with a commitment to innovation and exā€¦

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 ā€¦
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 devā€¦

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 curesā€¦
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 curesā€¦
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 curesā€¦
Experience: Senior level experience in software engineering, particularly in security and compliance.
Type: Full-time

Comind

Senior C++ Engineer London
Skills & Focus: C++, Python, software development, medical devices, IEC 62304, ISO 14971, Agile, risk analysis, healthcare technology, collaboration
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: 5+ years in software development, particularly for complex or safety-critical systems
Type: Full time
Benefits: Company equity plan, Company pension scheme, Private medical, dental and vision insurance, Group life assurance, Compreā€¦

Charlotte Tilbury Beauty

Global Quality Specialist London
Skills & Focus: quality management, skin care, cosmetics, product development, supplier management, quality assurance, KPI tracking, customer complaints, ISO standards, GMP
About the Company: Charlotte Tilbury Beauty is a global beauty brand founded in 2013, known for revolutionizing makeup application and operating in over 50 markets with more thanā€¦
Experience: Relevant experience in a quality role, preferably for skin care and/or gifting categories for cosmetics brands and in a fast-paced environment.
Benefits: 25 days holiday (plus bank holidays) plus birthday leave, inclusive parental leave policy, pension and life assurance, ā€¦

Orchard Therapeutics

Head of Pharmacovigilance London
Skills & Focus: Pharmacovigilance, Gene Therapy, Regulatory Compliance, Patient Safety, Global Strategy, Risk Assessment, Regulatory Submissions, Leadership, Biotech, Orphan Diseases
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 developā€¦

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 theā€¦
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

Senior Manager Clinical Data Standards High Wycombe
Skills & Focus: Clinical Data Standards, SDTM, Data Management, Regulatory Requirements, Data Transfer, Controlled Terminology, CRF, DTA, CDISC standards, GCP
About the Company: Johnson & Johnson is a multinational corporation focused on healthcare innovation, including pharmaceuticals, medical devices, and consumer health products.
Experience: At least 8 years in pharmaceutical/scientific fields, with minimum 5 years SDTM experience
Type: Full-time
Director Medical & Regulatory Excellence High Wycombe
Skills & Focus: Regulatory Affairs, Medical Excellence, Medical Operations, Cross-functional Teams, Quality System, Project Management, Leadership, Medical Compliance, Global Initiatives, Team Building
About the Company: A renowned healthcare company focused on innovative medicines and medical technologies.
Experience: Minimum of 5-7 yrs. of regulatory or medical affairs proven experience in relevant roles.
Type: Full-time

Ergomed

Senior PV Auditor Guildford
Skills & Focus: pharmacovigilance, audits, quality assurance, risk-based audit strategies, process improvements, audit reports, cross-functional teams, regulatory inspections, quality management systems, project management
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
Senior PV Auditor Guildford
Skills & Focus: pharmacovigilance, audits, compliance, risk-based, recommendations, cross-functional, regulatory inspections, mentorship, quality management, project management