Last updated: 2025-05-22

27 Quality Assurance And Engineering jobs in London.

Hiring now: Instrument Calibration En @ Perkinelme, Global Regulatory Affairs @ Karo Healt, Dir Lentiviral Vector @ Orchard Th, Vp Of Regulatory @ Flo Health, Supplier Governance Mgr @ Amgen, Sr Qara Engr Software @ Comind, Proj Cqv Engr @ Cai, Sr Mgr Regulatory Affairs @ Shionogi E, Mgr Global Supply Plannin @ Orchard, Regulatory Ops Document M @ Shionogi.Explore more at at kaamvaam.com

šŸ”„ Skills

compliance (7) regulatory compliance (5) collaboration (4) quality assurance (4) project management (4) regulatory inspections (4) biologics (3) medical devices (3) quality management (3) Senior Software Engineer (3)

šŸ“ Locations

London (19) Guildford (4) High Wycombe (2) Stevenage (1) Maidenhead (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

Karo Healthcare

Global Regulatory Affairs Manager Maidenhead
Skills & Focus: regulatory submissions, medicinal products, cross-functional, compliance, packaging, labeling, EU regulatory procedures, global experience, RIM systems, chance for growth
About the Company: Karo Healthcare, a dynamic and growing personal-care retail company, is all about making smart choices for everyday healthcare. With a wide-ranging portfolio aā€¦
Experience: 5+ years of experience in Regulatory Affairs, with a clear focus on medicinal products
Benefits: Opportunity to create, grow, and encourage; competitive salary pack; lots of growth opportunities; flexible schedule; rā€¦

Orchard Therapeutics

Director, Lentiviral Vector London
Skills & Focus: Lentiviral Vector, GMP production, biologics, process optimization, regulatory compliance, process validation, technical leadership, collaboration, quality assurance, manufacturing
About the Company: Orchard Therapeutics is a biopharmaceutical company focusing on the development and commercialization of gene therapies for patients with genetic diseases.
Experience: Minimum of 10 years in the biotechnology or pharma industry with a primary focus on upstream cell culture, downstream processing, and fill finish operations for biologics.
Type: Full-time

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

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 missionā€”to serve patientsā€”drives all that we do. It is key to our becoming one of the worldā€™s leading biotechnology companies. We are globā€¦
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.

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

Shionogi Europe

Senior Manager, Regulatory Affairs EU London
Skills & Focus: regulatory, EU, pharmaceutical, development, compliance, health authorities, collaboration, regulatory strategies, submission, inspection
About the Company: Shionogi is a pharmaceutical company dedicated to innovation and excellence in healthcare.
Experience: Experience in Regulatory Affairs within the pharmaceutical industry, with solid experience in development and some post-marketing experience.

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

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€¦

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 industrieā€¦
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.

Biomarin Pharmaceutical Inc.

Regulatory Data Steward London
Skills & Focus: Regulatory requirements, Regulatory data management, Drug development processes, Data quality monitoring, Regulatory Information Management, Veeva, SAP, Master Data Management, Change Management, Data governance
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 oā€¦
Experience: Greater than 5 years of experience in Regulatory Affairs, with 3 years in Regulatory Information Management/Data Stewardship

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€¦

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
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,ā€¦
Type: Hybrid

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