360 Quality Assurance Principles jobs in the United Kingdom
Quality Management Lead
Posted 3 days ago
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Job Description
Role: Quality Management Lead
Location: Bristol/Suffolk (Hybrid working available)
Type: Contract Rolling 12 months
Join one of the UK's most exciting megaprojects and help power the future.
Sizewell C is at the forefront of the UK's drive towards Net Zero, delivering dependable, low-carbon electricity for millions of homes. Following the success of Hinkley Point C, we're building the next generation of nuclear power - and we're looking for an experienced Quality Management Lead to ensure our supply chain meets the highest quality standards, right first time.
The role
As a Quality Management Lead, you'll be the single point of contact for all quality-related aspects within your assigned programme. You'll act as the "Intelligent Customer," ensuring suppliers deliver in line with contractual quality requirements from design through to construction and commissioning.
You will:
- Develop and implement Project Quality Control Plans and inspection strategies
- Review, accept and monitor Contractor Quality Assurance Plans
- Lead supplier audits and manage non-conformance resolution
- Oversee manufacturing and construction surveillance activities
- Collaborate closely with suppliers, inspection bodies, and internal stakeholders to ensure consistent, compliant, and efficient quality delivery
About you
Essential:
- Significant experience in quality assurance/control within major projects (nuclear or other safety-critical sectors preferred)
- Strong understanding of QA/QC best practices, ISO 9001, ISO 19443, and related standards
- Proven track record in supplier audits, inspections, and quality management processes
- Excellent communication, influencing, and relationship-building skills
- HNC/HND or degree in engineering/science (or equivalent)
Desirable:
- Nuclear new build experience
- Professional accreditation (e.g., IRCA auditor, CQI membership)
- French language skills
This vacancy is being advertised by Rullion Ltd acting as an employment business.
Since 1978, Rullion has been securing exceptional candidates for a range of clients; from large well-known brands to SMEs and start-ups. As a family-owned business, Rullion's approach is credible and honest, focused on building long-lasting relationships with both clients and candidates.
Rullion is a forward-thinking recruitment company that specialises in providing a wide range of talent consultancy services to a diverse client base, from small start-ups to large household names.
We celebrate and support diversity and are committed to ensuring equal opportunities for both employees and applicants.
Thanks
Rullion
Rullion celebrates and supports diversity and is committed to ensuring equal opportunities for both employees and applicants.
Quality Management Lead
Posted 3 days ago
Job Viewed
Job Description
Role: Quality Management Lead
Location: Bristol/Suffolk (Hybrid working available)
Type: Contract Rolling 12 months
Join one of the UK's most exciting megaprojects and help power the future.
Sizewell C is at the forefront of the UK's drive towards Net Zero, delivering dependable, low-carbon electricity for millions of homes. Following the success of Hinkley Point C, we're building the next generation of nuclear power - and we're looking for an experienced Quality Management Lead to ensure our supply chain meets the highest quality standards, right first time.
The role
As a Quality Management Lead, you'll be the single point of contact for all quality-related aspects within your assigned programme. You'll act as the "Intelligent Customer," ensuring suppliers deliver in line with contractual quality requirements from design through to construction and commissioning.
You will:
- Develop and implement Project Quality Control Plans and inspection strategies
- Review, accept and monitor Contractor Quality Assurance Plans
- Lead supplier audits and manage non-conformance resolution
- Oversee manufacturing and construction surveillance activities
- Collaborate closely with suppliers, inspection bodies, and internal stakeholders to ensure consistent, compliant, and efficient quality delivery
About you
Essential:
- Significant experience in quality assurance/control within major projects (nuclear or other safety-critical sectors preferred)
- Strong understanding of QA/QC best practices, ISO 9001, ISO 19443, and related standards
- Proven track record in supplier audits, inspections, and quality management processes
- Excellent communication, influencing, and relationship-building skills
- HNC/HND or degree in engineering/science (or equivalent)
Desirable:
- Nuclear new build experience
- Professional accreditation (e.g., IRCA auditor, CQI membership)
- French language skills
This vacancy is being advertised by Rullion Ltd acting as an employment business.
Since 1978, Rullion has been securing exceptional candidates for a range of clients; from large well-known brands to SMEs and start-ups. As a family-owned business, Rullion's approach is credible and honest, focused on building long-lasting relationships with both clients and candidates.
Rullion is a forward-thinking recruitment company that specialises in providing a wide range of talent consultancy services to a diverse client base, from small start-ups to large household names.
We celebrate and support diversity and are committed to ensuring equal opportunities for both employees and applicants.
Thanks
Rullion
Rullion celebrates and supports diversity and is committed to ensuring equal opportunities for both employees and applicants.
Quality Management Lead
Posted 2 days ago
Job Viewed
Job Description
Here, we believe that success comes from continuously pushing boundaries and working together to deliver on our promises. We embrace challenges with confidence and are dedicated to creating a secure and vibrant future for all.
We'll inspire and empower you to deliver your best work so you can evolve, grow and succeed - today and into tomorrow. We offer an exciting range of opportunities to develop your career within a supportive and diverse team who always strive to do the right thing for our people, clients and communities.
People are our greatest asset, and we offer a competitive package to retain and attract the best talent.
In addition to the benefits you'd expect, UK employees also receive free single medical cover and digital GP service, family-friendly benefits such as enhanced parental leave pay and free membership of employee assistance and parental programmes, plus reimbursement towards relevant professional development and memberships. We also give back to our communities through our Collectively program which incorporates matched-funding, paid volunteering time and charitable donations.
Work-life balance and flexibility is a key focus area for us. We're happy to discuss hybrid, part-time and flexible working hours, patterns and locations to suit you and our business.
**About the Opportunity**
Nuclear Power Programmes has been formed with the vision to support positive change and help shape the future of Nuclear Power.
Operational throughout the UK and across continental Europe, we are seeking to expand our team on a variety of nuclear projects, which range in technologies and that find themselves at different stages of their development. To do this, we are seeking to continuously employ talented individuals to join our diverse team that are excited about nuclear projects and are committed to Net Zero, and Energy Security.
In both client facing and internal roles we are delivering major programme and project management capabilities throughout the project lifecycle. We are driving to deliver safe, high quality and to time solutions by thinking innovatively and working collaboratively.
Amentum are recruiting for a Quality Management Lead to ensure supply-chain adherence to the contracted quality assurance and quality control requirements on the Sizewell C Project. You'll sit within the Project Delivery Office Quality Team and will be deployed to Programmes to serve this primary purpose. Day to day reporting is to the Quality Delivery Manager (QDM) who sets out the Programme quality requirements. This includes development and implementation of Project Quality Control Plans and associated inspection and surveillance activities. Key responsibilities will be:
+ Review, accept and monitor Contractors Quality Assurance Plans (CQAP) provided by the supply chain, identify needs for supply chain audits, perform audits and resolve findings.
+ Produce Project Quality Control Plans (PQCP) for each contract/project.
+ Ensure deployment of key quality contractual arrangements including the General Quality Assurance Specification (GQAS), Lifetime Quality Records (LTQR) Specification.
+ Release Certificate and the Inspection & Test Plan Specifications.
+ Provide relevant guidance to contractors, including contractor's CQAPs, LTQR partitioning strategies and the arrangements for identifying and planning for Quality Related Activities.
+ Lead the implementation of LTQR reviews.
+ Support the determination and application of strategies for progressive provision of LTQRs by contractors.
+ Develop and maintain effective relationships with internal and external stakeholders including contracted inspection entities.
+ Ensure manufacturing and construction surveillance per contract is applied in a graded approach of safety function and project importance.
+ Ensure overall effectiveness of ITPs submitted by the suppliers, checking that they are fit for purpose.
**Here's What You'll Need**
+ Experience in project delivery, with focus on project quality, with a solid understanding of the Quality Assurance and Quality Control in major projects.
+ Understanding of quality management best practice for deployment by large, complex and contract-led organisations.
+ Knowledge of Quality Systems, ISO 9001, ISO 19443, IAEA GSR-2 and interrelated standards.
+ Experience of interfacing with project teams and with supply chain organisations.
+ Analysis of data, preparing reports and making recommendations.
+ Able to build effective relationships with internal and external stakeholders.
+ Pro-active and flexible, being prepared to plan and work on own initiative.
**Our Culture**
Our values stand on a foundation of safety, integrity, inclusion and diversity. We put people at the heart of our business, and we genuinely believe that we all succeed by supporting one another through our culture of caring. We value positive mental health and a sense of belonging for all employees.
We aim to embed inclusion in everything we do. We know that if we are inclusive, we're more connected, and we're more creative. We accept people for who they are, regardless of age, disability, gender identity, gender expression, marital status, mental health, race, faith or belief, sexual orientation, socioeconomic background, and whether you're pregnant or on family leave. This is reflected in our wide range of Global Employee Networks.
We partner with VERCIDA to help us attract and retain diverse talent. For greater online accessibility, please visit to view and access our roles. As a Disability Confident employer, we will interview all disabled applicants who meet the minimum criteria for a vacancy. We welcome applications from candidates who are seeking flexible working and from those who may not meet all the listed requirements for a role.
If you require further support or reasonable adjustments with regards to the recruitment process (for example, you require the application form in a different format), please contact the team.
Amentum is proud to be an Equal Opportunity Employer. Our hiring practices provide equal opportunity for employment without regard to race, sex, sexual orientation, pregnancy (including pregnancy, childbirth, breastfeeding, or medical conditions related to pregnancy, childbirth, or breastfeeding), age, ancestry, United States military or veteran status, color, religion, creed, marital or domestic partner status, medical condition, genetic information, national origin, citizenship status, low-income status, or mental or physical disability so long as the essential functions of the job can be performed with or without reasonable accommodation, or any other protected category under federal, state, or local law. Learn more about your rights under Federal laws and supplemental language at Labor Laws Posters ( .
Quality Management Consultant - ISO
Posted today
Job Viewed
Job Description
Senior ISO Management Consultant (remote based in the South East / Home Counties with some travel to clients) required to support clients in implementing, designing and improving ISO Quality management systems / ISO Standards, with strong skills in Quality (ISO 9001), and least one of Health & Safety (ISO 45001), Environmental (ISO 14001) and Information Security (ISO 27001) is required by fast-growing innovative award-winning and specialist ISO Consultancy with offices near Tunbridge Wells, Kent and London to support a diverse range of private and public sector clients.
The remote role is based in the South East / Home Counties, and a car will be needed to travel to customer sites a few times per month.
As a Quality Management Consultant, the essential skills would include.
- Open-minded, consultative, and customer-centric person with experience advising external clients or implementing quality management systems internally within a complex business and supporting them in implementing and improving various ISO management systems.
- Proven hands-on experience in the implementation of ISO 9001 Standard and at least one of ISO 45001, ISO 14001 or ISO 27001
- Experience as an auditor in at least one of the following Standards: ISO 9001, ISO 45001, ISO 14001, ISO 27001 or ISO 50001.
- Highly effective interpersonal and communication skills
- Excellent report-writing skills
- Advanced Microsoft Office skills
- Involved in the design, implementation, operations, and maintenance of a multisite IMS / Integrated Management System.
- Excellent planning and organization skills to meet deadlines with a proven ability to deliver on-time, on-budget projects.
- A strong teamwork ethic
- Full driving licence and a car are required as the role involves some travel to client sites in London and within the UK.
The responsibilities of the Quality Management Consultant would include
- Managing a group of clients and multiple ISO projects
- Strong skills in time management and being self-motivated to advise and support your portfolio of clients
- Consulting with and supporting support clients in implementing, designing and improving ISO Quality management systems.
- Assist clients with drafting policies & procedures
- Collation of records & data required by the International Standards
- Ensuring the smooth project delivery
- Identify the legal, statutory, regulatory & contractual requirements applicable to the client.
- Identify risks & opportunities that are relevant to the client.
This is a great chance to join a busy and people-centric specialist ISO company with a strong client pipeline and flex your skills working with a diverse client base in the private and public sectors. The company will offer training and support to be a Lead Auditor.
Opus Resourcing acts as an employment agency with respect to permanent employment.
Sr Dir GD Quality Management (GVP)
Posted 13 days ago
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Job Description
As a member of the GDQGO Leadership Team, you will play an integral role in advancing our mission while fostering innovation, quality, and collaboration across global functions.
**A Typical Day:**
In this role, you will:
+ Lead the GDQM (GVP) sub-function, providing strategic direction and operational oversight.
+ Ensure proactive, risk-based approaches to quality and compliance within Regeneron's Quality Management System (QMS).
+ Collaborate with cross-functional teams to support Good Pharmacovigilance Practice (GVP), Good Clinical Practice (GCP), and Medical and Regulatory Affairs.
+ Oversee timely issue escalation, risk management activities, and inspection readiness.
+ Manage team resources, including hiring strategies, onboarding, and performance reviews.
+ Represent the GDQGO sub-function during regulatory inspections and cross-functional forums.
+ Drive process improvement initiatives and champion innovation to enhance quality objectives.
**This Role May Be For You If you:**
+ Are a strategic thinker with expert knowledge in GVP Quality and local affiliate QMS oversight.
+ Have a proven ability to lead cross-functional teams and build strong stakeholder relationships.
+ Thrive in a collaborative environment and are skilled at balancing strategic vision with operational execution.
+ Are adept at identifying risks and embedding proactive quality management approaches.
+ Possess exceptional communication skills and can effectively deliver key messages to executive leadership and cross-functional teams.
+ Excel at managing resources, fostering team growth, and driving large-scale quality initiatives.
**To Be Considered:**
We are looking for candidates with:
+ Extensive experience in quality management, particularly in GVP, GCP, and regulatory affairs.
+ A strong track record of leadership in global functions and cross-functional collaboration.
+ Expertise in risk-based quality management and inspection readiness strategies.
+ A passion for driving innovation and process improvement in quality systems.
+ Preferred qualifications include familiarity with Regeneron's global PV system and experience representing quality functions during regulatory inspections.
**Why Join Us?**
At Regeneron, we believe in the power of collaboration, innovation, and a commitment to excellence. As the Head of Global Development Quality Management (GVP), you will have the opportunity to make a meaningful impact on our mission to bring life-changing medicines to patients worldwide.
Join us and be part of a team that exemplifies quality, integrity, and leadership in every interaction.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
Quality Management Systems Sr Specialist, CAPA-Medical Devices
Posted today
Job Viewed
Job Description
As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.
**What You Can Expect**
Responsible for facilitating Corrective Action Preventive Action (CAPA) investigations in order to solve quality related problems. Resolve issues by identifying and applying solutions from acquired technical experience and guided precedents. Assist in planning and fulfilling investigation tasks, implementation tasks, and verification of effectiveness tasks by identifying and organizing activities into time dependent sequencing with realistic timelines. Ensure thorough documentation of all CAPA procedural requirements. Work effectively/productively with all departments by developing a team atmosphere. Responsible for ensuring CAPA files are audit ready. Interacts with many different functional departments, suppliers, and experts outside Zimmer to implement Zimmer Quality goals.
**How You'll Create Impact**
+ Provides coaching for CAPA investigation from initiation through containment, root cause analysis, implementation, and verification of effectiveness.
+ Provides facilitation and coaching on the problem solving process and challenges technical content.
+ Interfaces with CAPA owners/teams to coach and facilitate progression through CAPA process.
+ Assists with risk analysis of issue and ensures proper containment actions are applied.
+ Verifies all procedural CAPA requirements are met.
+ Assists to identify and escalate resource constraints/requirements, as applicable.
+ Reviews CAPA files to ensure the files are audit ready, clearly tell the story, contain all required objective evidence, etc.
+ Other quality tasks, as requested.
**What Makes You Stand Out**
+ Ability to work within a team environment and build relationships outside of the department
+ Strong interpersonal and conflict resolution skills.
+ Demonstrated CAPA experience
+ Detail oriented
+ Ability to deliver, meet deadlines and have results orientation.
+ Able to communicate both orally and in written form to multiple levels of the company.
+ Strong technical writing skills
+ Microsoft Office Suite, expert knowledge of root cause analysis, and understanding of QSR/ISO regulations.
+ Knowledge of statistics, process control, and process capability a plus
**Your Background**
+ ?English proficiency at a C1 (Advanced) level is required.
+ Bachelor's degree in engineering or an equivalent field.
+ Proven Corporate CAPA experience within the Medical Devices industry is essential.
+ Minimum of 5 years of experience in Quality and Corporate CAPA within the medical devices sector, with a demonstrated ability to lead, implement, analyze, and execute hands-on end-to-end CAPA processes.
+ Strong knowledge of quality standards, including ISO 13485, is required.
+ Experience working with global teams, particularly across North America (NAM) and Latin America (LATAM).
+ Certifications such as CQE (Certified Quality Engineer) or CRE (Certified Reliability Engineer) from the American Society for Quality (ASQ) are considered a strong plus.
+ A combination of education and relevant experience may be considered in evaluating qualifications.
**_Kindly ensure your resume is in English when applying, as applications in other languages cannot be considered._**
**Travel Expectations**
EOE/M/F/Vet/Disability
QA Specialist
Posted 4 days ago
Job Viewed
Job Description
SRG are working with a global name in the pharmaceutical industry to help them find a QA Specialist to join their team.
If you have Quality Assurance (QA) experience from a GMP environment then this could be a great next step for you.
The company offer an excellent benefits package and scope for growth and development.
The Role:
- Perform batch reviews within required timelines
- Author and review SOPs
- Document and report all work in adherence with GMP and departmental procedures
- Review change controls and provide feedback / corrections to authors and escalate concerns to the Quality Manager/Head of Quality where necessary
- Raise, approve and review CAPAs
- Represent the QA team for improvement projects and with clients and internal teams
- Assist in the performance of supplier audits, supporting the Lead Auditor
- Acts as a support to client and regulatory audits, helping with technical support to the audit team and responding to requests for documentation and information
- Conducts self-inspections / audits to ensure compliance with Quality Management System procedures and GMP regulations
- Ensuring that a timely and effective communication and escalation of quality issues to the appropriate levels of management
- Carries out site internal audits and identifies areas of GMP improvement during their daily duties
- Carries out training for QMS activities as defined by line management
Requirements:
- Degree in a relevant scientific, engineering or business discipline and/or relevant industry experience
- Several years' experience within Quality Assurance working to GMP guidelines
- Experience of working within a Quality Management System e.g. completing or reviewing QMS documentation (SOPs/Deviations /Investigations /CAPA)
- Experience of preparing and assisting in external audits with regulatory bodies such as FDA and MHRA
- Organised and attention to detail
- Strong communication skills across all levels
Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
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QA Specialist
Posted 7 days ago
Job Viewed
Job Description
SRG are working with a global name in the pharmaceutical industry to help them find a QA Specialist to join their team.
If you have Quality Assurance (QA) experience from a GMP environment then this could be a great next step for you.
The company offer an excellent benefits package and scope for growth and development.
The Role:
- Perform batch reviews within required timelines
- Author and review SOPs
- Document and report all work in adherence with GMP and departmental procedures
- Review change controls and provide feedback / corrections to authors and escalate concerns to the Quality Manager/Head of Quality where necessary
- Raise, approve and review CAPAs
- Represent the QA team for improvement projects and with clients and internal teams
- Assist in the performance of supplier audits, supporting the Lead Auditor
- Acts as a support to client and regulatory audits, helping with technical support to the audit team and responding to requests for documentation and information
- Conducts self-inspections / audits to ensure compliance with Quality Management System procedures and GMP regulations
- Ensuring that a timely and effective communication and escalation of quality issues to the appropriate levels of management
- Carries out site internal audits and identifies areas of GMP improvement during their daily duties
- Carries out training for QMS activities as defined by line management
Requirements:
- Degree in a relevant scientific, engineering or business discipline and/or relevant industry experience
- Several years' experience within Quality Assurance working to GMP guidelines
- Experience of working within a Quality Management System e.g. completing or reviewing QMS documentation (SOPs/Deviations /Investigations /CAPA)
- Experience of preparing and assisting in external audits with regulatory bodies such as FDA and MHRA
- Organised and attention to detail
- Strong communication skills across all levels
Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
QC / QA Specialist
Posted 7 days ago
Job Viewed
Job Description
We are working with a streetwear fashion company who are looking to hire a QC/QA to join their highly successful team. This role is to ensure all garments and fashion products meet the required quality standards before production,
during production, and prior to shipment. The QC/QA specialist plays a key role in monitoring product specifications, identifying defects, ensuring compliance with brand.
WHJS1_UKTJ
Quality Process Management Lead - FSP - Remote
Posted 6 days ago
Job Viewed
Job Description
This role leads the development of departmental metrics and other reporting activities; facilitates/contributes to the process evaluation and integration of acquired company and/or asset related programs into Pfizer processes; contributes to compliance and audit/inspection readiness strategies and plans; and is responsible for ensuring high quality execution of controlled procedural documentation management
**Some specifics about this advertised role**
+ Accountable to manage and implement the quality oversight plan for the process portal content containing 42,000 informational objects pertaining to process quality standards, global and local country & functional area.
+ Act as a key subject matter expert in the process framework, process architecture, process modelling or standards and conventions. Advise, coach and train CMCD authors, Document Specialists, Process Owners, and other process experts.
+ Oversee the activities of procedural document compliance staff; maintain consistent workflow, prioritize needs, and establish coverage, provide coaching and guidance to staff members.
+ Facilitate/oversee the accuracy and completeness of process portal data by evaluating queries, performing data reviews, and reconciling findings to ensure accurate reporting.
**Who are Parexel**
Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.
We supported the trials of most of today's top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.
You'll be an influential member of the wider team.
**What we are looking for in this role**
For every role, we look for professionals who have the determination and courage always to put patient well-being first.
That to us is working with heart.
**Here are a few requirements specific to this advertised role** .
+ A scientific or technical degree is preferred.
+ Specific training around:
+ Process modelling, design, analysis and improvement methodologies and tools
+ Data analytics, including data connections, query design, chart/visual development and tools
+ BS and over 7 years; MS and over 5 years, or 10 years relevant experience in pharmaceutical industry.
+ Experience in process design and modelling methods, demonstrated ability to design effective processes.
+ Demonstrated experience in project management and implementation techniques.
+ Previous continuous improvement experience considered a plus.
+ A strong working knowledge and understanding of drug development processes, database structures, relational database management software, and data analysis tools.
#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.