37 Quality Assurance Manager jobs in London

Why Superdrug?

Passionate about Beauty and Health? Want to be part of an innovative, trend setting retailer? Our vibrant Head Office, based by East Croydon station is a fantastic environment filled with hundreds of brilliant personalities.

We’re a team that puts our customers and our teams at the heart of everything we do. At Superdrug, we aim to be the best in accessible health & beauty, loved by our customers for value, choice, friendly advice, service and fun.

Our success comes from our people – they make the difference. We’re all about personality, we have fun, and we work hard to deliver That Superdrug feeling.

You will manage Own Brand product development, quality and supplier base across various assigned categories by working closely with commercial, design and supply chain colleagues.

Deliver the agreed NPD plans by providing technical expertise throughout the new product development process and ensure pre and post launch product compliance and supplier compliance with both ASW Guidelines and existing regulatory requirements.

Here's the exciting bit…a great day includes

Develop Own Brand product ranges across all of our categories with the commercial team; setting out the technical and corporate social responsibility requirements.

Ensure all suppliers comply with and maintain compliance with ASW requirements.

Deliver the technical elements of the New Product Development process and ensure ongoing product and supplier compliance with ASW guidelines and relevant legal requirements.

Deliver the technical aspects of all critical paths to budget/cost and within set timescales.

Technical Expert – be an expert source of technical information, standards and legal requirements across all of our categories

Develop build and maintain effective working relationships with both internal and external stakeholders.

Continually keep up to date with technical innovation to ensure we develop exciting market leading products

Undertake store and supplier visits

As a Senior Quality Control Manager you will be managing a small team and will be involved in the development and growth of the Superdrug technical team .

Key Stakeholders

Internal

Own Brand team, Commercial team, Store operations, Customer relations, Legal, ASW Group Technical

External

Suppliers, Test houses, Industry Experts, Fragrance houses, Raw material suppliers.

What you’ll need to succeed

Must have a degree or equivalent in Cosmetic Science

8 years plus in Cosmetics & Toiletries. Healthcare experience would be an advantage.

Managing and coaching experience of junior team members would be an advantage

Proven experience working in fast paced commercial environment

Commercial acumen

Excellent communication skills and attention to detail

Ability to work to deadline and prioritise workload

Able to work on own initiative and problem solve

Team player

Resilient

This role requires a strong mix of technical knowledge, organisational skills, and the ability to work with a wide range of stakeholders. Also required, is the ability to balance the need for compliance and diligence with the commercial need for development at pace.

Here's what's in it for you

• 33 days holiday rising to 38 days with length of service (inclusive of bank holidays)
• 2 staff discount codes for yourself and a family member or friend
• 30% discount on Superdrug Own Brand Products both in store and online
• Hybrid working patterns available depending on role responsibilities with 2 days working from home and 3 days in our stylish, modern and collaborative office close to East Croydon Station
• Company pension matching and bonus
• We offer Wagestream - a money management app that gives you access to a percentage of your pay as you earn it
• Being part of more! We are part of a group who work closely with Savers, The Perfume Shop and Three UK
• We are part of A.S. Watson Group, the world's largest international health and beauty retailer with over 15,700 stores in 25 markets!
• Unrivalled Learning and Development programmes
• Enhanced maternity/shared parental/adoption leave, company sick pay and pregnancy loss and support

Come and be part of something special.

Hours : 37.5 | 9.00am - 5.30pm - Hybrid working available depending on role responsibilities with 2 days working from home and 3 days in our stylish, modern and collaborative office close to East Croydon Station.

For information on how we manage and store your data please go to

Why Superdrug?

Passionate about Beauty and Health? Want to be part of an innovative, trend setting retailer? Our vibrant Head Office, based by East Croydon station is a fantastic environment filled with hundreds of brilliant personalities.

We’re a team that puts our customers and our teams at the heart of everything we do. At Superdrug, we aim to be the best in accessible health & beauty, loved by our customers for value, choice, friendly advice, service and fun.

Our success comes from our people – they make the difference. We’re all about personality, we have fun, and we work hard to deliver That Superdrug feeling.

You will manage Own Brand product development, quality and supplier base across various assigned categories by working closely with commercial, design and supply chain colleagues.

Deliver the agreed NPD plans by providing technical expertise throughout the new product development process and ensure pre and post launch product compliance and supplier compliance with both ASW Guidelines and existing regulatory requirements.

Here's the exciting bit…a great day includes

Develop Own Brand product ranges across all of our categories with the commercial team; setting out the technical and corporate social responsibility requirements.

Ensure all suppliers comply with and maintain compliance with ASW requirements.

Deliver the technical elements of the New Product Development process and ensure ongoing product and supplier compliance with ASW guidelines and relevant legal requirements.

Deliver the technical aspects of all critical paths to budget/cost and within set timescales.

Technical Expert – be an expert source of technical information, standards and legal requirements across all of our categories

Develop build and maintain effective working relationships with both internal and external stakeholders.

Continually keep up to date with technical innovation to ensure we develop exciting market leading products

Undertake store and supplier visits

As a Senior Quality Control Manager you will be managing a small team and will be involved in the development and growth of the Superdrug technical team .

Key Stakeholders

Internal

Own Brand team, Commercial team, Store operations, Customer relations, Legal, ASW Group Technical

External

Suppliers, Test houses, Industry Experts, Fragrance houses, Raw material suppliers.

What you’ll need to succeed

Must have a degree or equivalent in Cosmetic Science

8 years plus in Cosmetics & Toiletries. Healthcare experience would be an advantage.

Managing and coaching experience of junior team members would be an advantage

Proven experience working in fast paced commercial environment

Commercial acumen

Excellent communication skills and attention to detail

Ability to work to deadline and prioritise workload

Able to work on own initiative and problem solve

Team player

Resilient

This role requires a strong mix of technical knowledge, organisational skills, and the ability to work with a wide range of stakeholders. Also required, is the ability to balance the need for compliance and diligence with the commercial need for development at pace.

Here's what's in it for you

• 33 days holiday rising to 38 days with length of service (inclusive of bank holidays)
• 2 staff discount codes for yourself and a family member or friend
• 30% discount on Superdrug Own Brand Products both in store and online
• Hybrid working patterns available depending on role responsibilities with 2 days working from home and 3 days in our stylish, modern and collaborative office close to East Croydon Station
• Company pension matching and bonus
• We offer Wagestream - a money management app that gives you access to a percentage of your pay as you earn it
• Being part of more! We are part of a group who work closely with Savers, The Perfume Shop and Three UK
• We are part of A.S. Watson Group, the world's largest international health and beauty retailer with over 15,700 stores in 25 markets!
• Unrivalled Learning and Development programmes
• Enhanced maternity/shared parental/adoption leave, company sick pay and pregnancy loss and support

Come and be part of something special.

Hours : 37.5 | 9.00am - 5.30pm - Hybrid working available depending on role responsibilities with 2 days working from home and 3 days in our stylish, modern and collaborative office close to East Croydon Station.

For information on how we manage and store your data please go to -policy/

Are you a QA/QC expert ready to ensure absolute precision across Civil, Structural, Architectural (CSA), Mechanical, and Electrical (M&E) disciplines on world-class projects?

Salter Grange is partnering with a Leading Principal Contractor —a forward-thinking powerhouse in the Mission Critical Data Centre sector. With a full order book for several years , this is a unique opportunity for a credible QA/QC Manager to play a pivotal role in the company's growth and expansion.

This is your chance to join a cutting-edge business, secure your career for the long term, and establish the quality benchmark for projects that power the digital world.

QA Manager Responsibilities:

You will be the authority on quality, interpreting client requirements and driving flawless execution across multi-discipline systems. Your focus is ensuring smooth, system-by-system handover.

• Coordinate the creation, execution, and upkeep of the project Quality Plan and all associated Inspection/Test Plans (ITPs) per Client specifications.
• Clearly interpret and communicate complex contract Quality requirements to all project staff and supporting company functions.
• Review, audit, and manage the implementation of the Project Quality plan and procedures, working closely with the Auditing team.
• Expertly manage Project inspection/test programs and all crucial witness point schedules on a system-by-system basis, ensuring full client participation.
• Manage the resolution of all quality-related matters at the Project Management and supervisor levels.
• Coordinate the meticulous handover of all final Quality Records to the Client on a system-by-system basis.

QA Manager Requirements:

• Significant experience covering CSA, Mechanical, and Electrical systems.
• 3-5 years of experience in a similar QA/QC Construction role.
• Prior experience on Data Centre or equivalent large industrial/mission-critical projects is essential.
• Previous experience working for a General/Principal Contractor is ideal.

Must possess the right to work in Europe (EU Passport/Visa).

APPLY NOW via the link, or contact Julia at to discuss this career-accelerating opportunity further.

• Lead and manage the Quality Assurance department, ensuring compliance with all relevant regulations.
• Develop, implement, and maintain the Quality Management System (QMS).
• Oversee all GMP activities, including batch record review, release, and deviations.
• Conduct internal audits and host regulatory inspections.
• Manage and investigate deviations, root cause analyses, and implement corrective and preventive actions (CAPAs).
• Review and approve validation protocols and reports.
• Provide QA support and training to other departments.
• Stay current with evolving regulatory requirements and industry best practices.
• Manage vendor quality agreements and conduct supplier audits.
• Contribute to strategic quality initiatives and process improvements.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Life Sciences, or a related field.
• Extensive experience (e.g., 8+ years) in Pharmaceutical Quality Assurance.
• In-depth knowledge of GMP, GDP, and other relevant pharmaceutical regulations (e.g., MHRA, FDA).
• Proven experience in managing audits (internal, external, regulatory).
• Strong understanding of validation principles and documentation.
• Excellent leadership, team management, and interpersonal skills.
• Proficiency in quality risk management and problem-solving methodologies.
• Exceptional attention to detail and strong analytical skills.
• Ability to effectively communicate with senior management and regulatory bodies.

• Develop, implement, and maintain the Quality Management System (QMS) compliant with GMP and other relevant regulations.
• Oversee all QA activities, including batch record review, release, deviations, change control, and CAPA management.
• Conduct internal audits of manufacturing processes, facilities, and documentation.
• Participate in external audits and inspections by regulatory authorities (e.g., MHRA, FDA, EMA).
• Manage the qualification and validation of equipment, processes, and analytical methods.
• Ensure the quality and compliance of raw materials, packaging materials, and finished products.
• Lead and mentor the QA team, fostering a culture of quality and continuous improvement.
• Collaborate with R&D, Manufacturing, and Regulatory Affairs departments to ensure product quality and compliance.
• Review and approve validation protocols and reports.
• Manage supplier quality, including audits and quality agreements.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 7 years of experience in Quality Assurance within the pharmaceutical industry.
• In-depth knowledge of GMP, GDP, ICH guidelines, and other relevant regulatory requirements.
• Proven experience in managing QMS, deviations, CAPAs, change control, and audits.
• Experience with regulatory inspections and submissions.
• Strong leadership and team management skills.
• Excellent analytical, problem-solving, and decision-making abilities.
• Proficiency in quality risk management principles.
• Exceptional written and verbal communication skills.

• Develop, implement, and maintain robust Quality Management Systems (QMS) in accordance with GMP, ICH, and other relevant regulatory guidelines.
• Lead and manage the Quality Assurance team, providing guidance, mentorship, and performance management.
• Oversee all QA activities, including batch record review and release, deviation management, CAPA implementation, change control, and complaint handling.
• Conduct internal and external audits (including vendor audits) to ensure compliance and identify areas for improvement.
• Prepare for and host regulatory inspections (e.g., MHRA, FDA), ensuring successful outcomes.
• Collaborate with R&D, Manufacturing, Regulatory Affairs, and other departments to ensure quality is integrated throughout the product lifecycle.
• Manage validation activities, including process validation, cleaning validation, and equipment qualification.
• Develop and deliver quality training programs for site personnel.
• Monitor quality metrics and trends, identifying potential risks and implementing risk mitigation strategies.
• Ensure all activities are conducted in compliance with company policies and regulatory requirements.
• Drive continuous improvement initiatives within the QA department and across the site.
• Review and approve product quality reviews (PQRs) and annual product quality summaries.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field. Advanced degree preferred.
• Minimum of 10 years of experience in Pharmaceutical Quality Assurance, with at least 3-5 years in a management role.
• Extensive knowledge of GMP regulations and guidelines applicable to pharmaceutical manufacturing.
• Proven experience in managing and conducting audits, inspections, and regulatory submissions.
• Strong understanding of pharmaceutical manufacturing processes, product development, and quality control.
• Excellent leadership, team management, and interpersonal skills.
• Exceptional analytical, problem-solving, and decision-making abilities.
• Strong understanding of validation principles and practices.
• Proficiency in using QMS software and standard office applications.
• Excellent written and verbal communication skills, with the ability to articulate complex quality concepts clearly.

Are you a QA/QC expert ready to ensure absolute precision across Civil, Structural, Architectural (CSA), Mechanical, and Electrical (M&E) disciplines on world-class projects?

Salter Grange is partnering with a Leading Principal Contractor —a forward-thinking powerhouse in the Mission Critical Data Centre sector. With a full order book for several years , this is a unique opportunity for a credible QA/QC Manager to play a pivotal role in the company's growth and expansion.

This is your chance to join a cutting-edge business, secure your career for the long term, and establish the quality benchmark for projects that power the digital world.

QA Manager Responsibilities:

You will be the authority on quality, interpreting client requirements and driving flawless execution across multi-discipline systems. Your focus is ensuring smooth, system-by-system handover.

• Coordinate the creation, execution, and upkeep of the project Quality Plan and all associated Inspection/Test Plans (ITPs) per Client specifications.
• Clearly interpret and communicate complex contract Quality requirements to all project staff and supporting company functions.
• Review, audit, and manage the implementation of the Project Quality plan and procedures, working closely with the Auditing team.
• Expertly manage Project inspection/test programs and all crucial witness point schedules on a system-by-system basis, ensuring full client participation.
• Manage the resolution of all quality-related matters at the Project Management and supervisor levels.
• Coordinate the meticulous handover of all final Quality Records to the Client on a system-by-system basis.

QA Manager Requirements:

• Significant experience covering CSA, Mechanical, and Electrical systems.
• 3-5 years of experience in a similar QA/QC Construction role.
• Prior experience on Data Centre or equivalent large industrial/mission-critical projects is essential.
• Previous experience working for a General/Principal Contractor is ideal.

Must possess the right to work in Europe (EU Passport/Visa).

APPLY NOW via the link, or contact Julia at to discuss this career-accelerating opportunity further.

Pensions Quality Assurance Manager (ref: )

We’re seeking a strong pensions technical professional for a newly created Quality Assurance Manager role. Lead the development of QA frameworks across key pensions areas including GMP Equalisation, Pensions Dashboards, and core administration.

UK Wide locations with hybrid working

This will suit someone within a quality driven role or an Admin Manager/Team Leader with good experience across process/technical areas

Key Responsibilities

• Lead and develop a high-performing QA team.
• Implement and maintain QA frameworks and tools.
• Ensure data accuracy and regulatory compliance.
• Oversee audit and certification processes
• Provide technical support across TPA functions
• Support Pensions Dashboard integration and data readiness.
• Monitor QA KPIs and report insights to leadership.
• Collaborate with internal teams and stakeholders.

What You’ll Bring

• Strong knowledge of DB and DC schemes.
• Leadership and stakeholder management skills.
• Experience in a TPA environment is a plus.
• Familiarity with audit and certification standards.

Please quote reference . If you know someone suitable for this role, share the word and through our referral scheme receive up to £250! Click here for further details on our recommendation scheme.

This is just one of the many roles we are working on at the Sammons Recruitment Group. Please visit our website for full details on all Permanent, Temporary and Contract career opportunities we are actively seeking candidates for. Recruiting on the basis of Talent, we are committed to supporting and promoting diversity in the workplace and consider all applications. Any salary advertised is for search purposes only. If you have not heard from us within 7 days you will have not been successful on this occasion, however, we would welcome your application for alternative vacancies.

• Develop, implement, and manage comprehensive Quality Management Systems (QMS) in alignment with global pharmaceutical standards (e.g., FDA, EMA, MHRA).
• Oversee and ensure compliance with Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and other relevant GxP guidelines.
• Lead and conduct internal and external audits to assess compliance and identify areas for improvement.
• Manage the deviation and CAPA (Corrective and Preventive Actions) systems, ensuring timely investigation and resolution.
• Review and approve essential quality-related documents, including batch records, validation protocols, and change controls.
• Provide expert guidance and training to personnel on quality assurance principles and regulatory requirements.
• Act as a key point of contact for regulatory agency inspections, facilitating smooth and successful outcomes.
• Monitor quality metrics, identify trends, and implement strategies to enhance product quality and process efficiency.
• Lead and mentor a team of QA professionals, fostering a culture of quality and compliance.
• Collaborate with cross-functional teams, including R&D, manufacturing, and regulatory affairs, to ensure quality is integrated throughout the product lifecycle.
• Stay current with evolving regulatory landscapes and industry best practices.

• Advanced degree in Pharmacy, Chemistry, Biology, or a related life science discipline.
• Minimum of 10 years of progressive experience in Pharmaceutical Quality Assurance, with a significant portion in a managerial or leadership capacity.
• Extensive knowledge of GxP regulations (GMP, GCP, GLP) and international regulatory guidelines.
• Proven experience in developing and implementing robust Quality Management Systems.
• Demonstrated experience in conducting and managing audits (internal and external).
• Strong understanding of pharmaceutical product development, manufacturing, and lifecycle management.
• Excellent leadership, communication, analytical, and problem-solving skills.
• Ability to manage multiple projects and prioritize effectively in a remote setting.
• Experience interacting with regulatory agencies (FDA, EMA, MHRA) is essential.
• Proficiency in quality management software and tools.
• Must be legally eligible to work in the UK and able to work remotely.