Explore opportunities as a Quality Director, a pivotal role focused on maintaining and improving organizational standards. These positions demand expertise in 1,028 Quality Director jobs in the United Kingdom
Design Assurance Quality Director
Posted 6 days ago
Job Viewed
Job Description
Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With more than 10,000 colleagues, we provide our products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec's revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more please visit Key Responsibilities** :
+ Lead, mentor, coach, and develop team of technical Quality Assurance professionals who collaborate with T&I on the design, development, and manufacturing transfer of new or changed medical device products.
+ Ensure appropriate application of company policies and procedures for product development, risk management, test method development, statistical data analysis, and support of regulatory filings.
+ Lead the continuous improvement of the quality system elements that support the design, development, and manufacturing transfer of new products.
+ Maintain oversight of cGMP documentation, including, but not limited to product development reports, change control, validations, methods, and technology transfer.
+ Ensure documents are thorough, accurate and compliant to support regulatory inspections and submissions.
+ Provide support for investigations and recommend, develop and implement effective corrective actions.
+ Provides support during regulatory inspections and customer audits.
+ Identify and implement quality system improvements when gaps are identified through audits and departmental reviews.
+ Proactively investigates, identifies and implements improved quality practices.
+ Ensure operations within approved department budget.
+ Responsible for personnel actions including hiring, performance management, and termination.
+ Ensures compliance in compiling and maintenance of Design History Files.
+ Drives a consistent approach to Design Controls across all the business units in ConvaTec.
+ Define and manage KPIs for related Quality Management Systems, in partnership with T&I
+ Ensures timely investigations and implementation of corrective actions related to design.
+ Permanent quality member for stage gate reviews/approvals.
+ Part of the T&I extended leadership team.
+ Part of the GDC site leadership team, including quality oversight of test laboratories that execute design validation, verification, and stability studies.
+ Management representative for GDC.
+ Ensures that QMS requirements are effectively established, implemented, maintained, and documented in accordance with standards and regulations identified in the reference section of the quality manual.
+ Reporting to management on the effectiveness of the quality management system and any needs for improvement.
+ Ensuring the promotion of awareness of the applicable regulatory and QMS requirements throughout the organization.
+ Ensuring quality policy is understood, implemented, and maintained at all levels of convatec.
+ Have oversight and support quality activities at the convatec Canada Ltd site as well as the Boston development site, ensuring compliance on the execution of the processes.
+ Lead 3rd party due diligence related to design quality/design controls.
+ Lead, direct, or execute vendor approval audits related to new product introductions.
+ Direct a team of design assurance and quality system managers with direct assignments to each business unit, ensuring close partnership with T&I on the development & launch of new products. This team covers design activities at all locations across convatec, and includes software as a medical device.
+ Has a total of minimum 7 direct reports, including global process owners for critical technical functions that impact all of convatec (risk management and statistical techniques).
**What we are looking for in you :**
+ Breadth of professional field and industry knowledge.
+ Experience working in Quality Systems/Processes that cover Medical Device Design Controls and Pharmaceutical Development preferred.
+ Ability to integrate critical information and champion advanced strategies/concepts through the organization.
+ Drives development of advanced technologies, principles and processes.
+ Ensures budgets, schedules, and performance requirements are met.
+ Judgement is required in resolving complex problems based on experience.
+ The ability to work in a cross functional team and ensure compliant project execution is a must.
+ Deep understanding of Design Controls and Design Change Process
+ Experience working in international environment in a global position is preferred
+ Minimum of B.S., or equivalent, in a scientific/technical discipline is required. Advanced degree (M.S., M.B.A, Ph.D. or equivalent) preferred.
+ Certifications in Quality Management Systems preferred.
+ Ten+ (10+) years in the medical device and/or pharmaceutical industry.
+ Five to seven (5-7) years experience in a leadership role.
+ Practical experience and global mastery in global quality standards and regulations governing medical products.
+ Written and spoken English. Another language would be an advantage
**Key competencies :**
+ Ability to think in clear, decisive manner, remaining calm under stressful and challenging conditions.
+ Ability to efficiently work through quality, organization and business issues with a focus on solutions and proactive contingency planning in support of the customer and business objectives.
+ Ability to apply budgetary analysis principles and effective allocation of internal/external resources.
+ Understanding of risk management principles and ability to apply these principles in day to day quality management activities, compliance issues, and business challenges.
+ Commercially astute and customer focused.
The role will require c25% travel
**Ready to join us?**
At Convatec, we're pioneering trusted medical solutions to improve the lives we touch. If you're ready to make a real impact, apply today and help us bring our Forever Caring promise to life.
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**Beware of scams online or from individuals claiming to represent Convatec**
A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.
If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you're unsure, please contact us at .
**Equal opportunities**
Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.
**Notice to Agency and Search Firm Representatives**
Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
**Already a Convatec employee?**
**If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!**
Quality Manager / Director
Posted 4 days ago
Job Viewed
Job Description
Meritus are recruiting for a long-established but fast-growing precision engineering business with over 30 years' history supplying the defence sector. Specialising in the manufacture of high-value, high-precision mechanical components, the company plays a vital role in supporting UK defence infrastructure. With a current 32,000 sq ft facility and expansion into a new 27,000 sq ft site, this is an exciting time to join as they scale operations into new markets and projects.
The Opportunity
This is a board-level appointment and a pivotal role in shaping the future of the company. The Quality Director will be responsible for the overall quality management strategy across the business, ensuring compliance with AS9100 standards and maintaining the highest level of customer and regulatory confidence. The role offers significant growth potential, evolving into a group-level responsibility across multiple sites as the business expands.
Key Responsibilities
- Own, maintain, and continuously improve the company's Quality Management System (QMS) to AS9100 standards.
- Lead and facilitate internal and external audits, ensuring full compliance with customer and regulatory requirements.
- Drive a culture of quality across the organisation, embedding best practices and continuous improvement initiatives.
- Manage and mentor the quality team, ensuring they are empowered to maintain operational excellence.
- Collaborate with cross-functional teams including engineering, production, and business development to resolve quality challenges quickly and effectively.
- Act as a board-level representative for quality, influencing long-term strategy and supporting the company's ambitious growth plans.
- Support the roll-out of quality processes into a second manufacturing facility and across group companies.
Skills and Experience Required
- Proven experience in a senior quality role within defence or aerospace manufacturing.
- Strong knowledge of AS9100 requirements and hands-on experience managing successful audits.
- Ability to manage multiple priorities, adapt to fast-moving situations, and solve problems under pressure.
- Background in mechanical engineering or machining is highly desirable but not essential.
- Strong leadership and communication skills, with the ability to influence at board level and motivate teams at all levels.
- Eligible to work in the UK. Security clearance is not essential but would be advantageous.
What's on Offer
- Salary in the region of 60,000 - 80,000 depending on experience.
- Flexible working arrangements for the right candidate.
- Early finish on Fridays.
- Direct impact on business strategy and the opportunity to grow into a group-level leadership role.
- The chance to work on high-value, prestigious defence projects that contribute directly to national security.
Working Hours
- Monday to Thursday: 8:00 - 16:45 (half-hour lunch)
- Friday: 8:00 - 15:30 (early finish)
Quality Manager / Director
Posted 4 days ago
Job Viewed
Job Description
Meritus are recruiting for a long-established but fast-growing precision engineering business with over 30 years' history supplying the defence sector. Specialising in the manufacture of high-value, high-precision mechanical components, the company plays a vital role in supporting UK defence infrastructure. With a current 32,000 sq ft facility and expansion into a new 27,000 sq ft site, this is an exciting time to join as they scale operations into new markets and projects.
The Opportunity
This is a board-level appointment and a pivotal role in shaping the future of the company. The Quality Director will be responsible for the overall quality management strategy across the business, ensuring compliance with AS9100 standards and maintaining the highest level of customer and regulatory confidence. The role offers significant growth potential, evolving into a group-level responsibility across multiple sites as the business expands.
Key Responsibilities
- Own, maintain, and continuously improve the company's Quality Management System (QMS) to AS9100 standards.
- Lead and facilitate internal and external audits, ensuring full compliance with customer and regulatory requirements.
- Drive a culture of quality across the organisation, embedding best practices and continuous improvement initiatives.
- Manage and mentor the quality team, ensuring they are empowered to maintain operational excellence.
- Collaborate with cross-functional teams including engineering, production, and business development to resolve quality challenges quickly and effectively.
- Act as a board-level representative for quality, influencing long-term strategy and supporting the company's ambitious growth plans.
- Support the roll-out of quality processes into a second manufacturing facility and across group companies.
Skills and Experience Required
- Proven experience in a senior quality role within defence or aerospace manufacturing.
- Strong knowledge of AS9100 requirements and hands-on experience managing successful audits.
- Ability to manage multiple priorities, adapt to fast-moving situations, and solve problems under pressure.
- Background in mechanical engineering or machining is highly desirable but not essential.
- Strong leadership and communication skills, with the ability to influence at board level and motivate teams at all levels.
- Eligible to work in the UK. Security clearance is not essential but would be advantageous.
What's on Offer
- Salary in the region of 60,000 - 80,000 depending on experience.
- Flexible working arrangements for the right candidate.
- Early finish on Fridays.
- Direct impact on business strategy and the opportunity to grow into a group-level leadership role.
- The chance to work on high-value, prestigious defence projects that contribute directly to national security.
Working Hours
- Monday to Thursday: 8:00 - 16:45 (half-hour lunch)
- Friday: 8:00 - 15:30 (early finish)
Quality Manager / Director
Posted 4 days ago
Job Viewed
Job Description
Meritus are recruiting for a long-established but fast-growing precision engineering business with over 30 years' history supplying the defence sector. Specialising in the manufacture of high-value, high-precision mechanical components, the company plays a vital role in supporting UK defence infrastructure. With a current 32,000 sq ft facility and expansion into a new 27,000 sq ft site, this is an.
WHJS1_UKTJ
Quality Control
Posted 4 days ago
Job Viewed
Job Description
Quality Control
Our client based in Ashbourne is looking for an experienced Quality Control person to work temporarily.
Monday, Tuesday, and Wednesday on a rotating 9-hour shift.
Hours for each week will be either 6am - 3pm, 8am - 5pm or 9am - 6pm.
12.69 per hour
The main duties for Quality Control:
* Inspecting and booking in of raw material deliveries
* Collection, Inspection and filing of finished product samples
* Processing customer returns
* In the mill/ office 50/50
* Need to have some basic IT skills
* Quality or feed experience would be fab but not essential
If you are interested for more information regarding this role, call Gi Group Derby or send your CV
Should you require any support or assistance, please contact your local Gi Group office.
Gi Group Holdings Recruitment Limited are proud founding members of Menopause in business, pledge members for Neurodiversity in business, Disability committed members, Silver status pledge members for the Armed Forces Covenant, and Bronze trail blazers for Racial Equality matters.
Gi Group Holdings Recruitment Limited group of companies includes Gi Recruitment Limited, Draefern Limited, Gi Group Recruitment Ltd, INTOO (UK) Limited, Marks Sattin (UK) Limited, TACK TMI UK Limited, Grafton Professional Staffing Limited, Encore Personnel Services, Gi Group Ireland Limited and Kelly Services (UK) Ltd. Gi Group Ireland Limited are acting as an Employment Agency in relation to this role.
We are committed to protecting the privacy of all our candidates and clients. If you choose to apply, your information will be processed in accordance with the Gi Group Privacy Statement. To view a copy and to help you understand how we collect, use and process your personal data please visit the Privacy page on our Gi Group website.
Quality Control
Posted 4 days ago
Job Viewed
Job Description
Quality Control
Our client based in Ashbourne is looking for an experienced Quality Control person to work temporarily.
Monday, Tuesday, and Wednesday on a rotating 9-hour shift.
Hours for each week will be either 6am - 3pm, 8am - 5pm or 9am - 6pm.
12.69 per hour
The main duties for Quality Control:
* Inspecting and booking in of raw material deliveries
* Collection, Inspection and filing of finished product samples
* Processing customer returns
* In the mill/ office 50/50
* Need to have some basic IT skills
* Quality or feed experience would be fab but not essential
If you are interested for more information regarding this role, call Gi Group Derby or send your CV
Should you require any support or assistance, please contact your local Gi Group office.
Gi Group Holdings Recruitment Limited are proud founding members of Menopause in business, pledge members for Neurodiversity in business, Disability committed members, Silver status pledge members for the Armed Forces Covenant, and Bronze trail blazers for Racial Equality matters.
Gi Group Holdings Recruitment Limited group of companies includes Gi Recruitment Limited, Draefern Limited, Gi Group Recruitment Ltd, INTOO (UK) Limited, Marks Sattin (UK) Limited, TACK TMI UK Limited, Grafton Professional Staffing Limited, Encore Personnel Services, Gi Group Ireland Limited and Kelly Services (UK) Ltd. Gi Group Ireland Limited are acting as an Employment Agency in relation to this role.
We are committed to protecting the privacy of all our candidates and clients. If you choose to apply, your information will be processed in accordance with the Gi Group Privacy Statement. To view a copy and to help you understand how we collect, use and process your personal data please visit the Privacy page on our Gi Group website.
Quality Control
Posted 10 days ago
Job Viewed
Job Description
The role of the Quality Control is to ensure that our product is always acceptable and meets the correct, Specification as well as promoting the benefits of high standards of Product Quality. Quality Control will aid the efficiency of the business by ensuring that the product is right first time. This role includes taking product samples and supporting the wider quality/ technical team.
Your main accountabilities will be to:
- Measure quality assurance at production level against confirmed specifications
- Work alongside Production Operatives to ensure quality is a pivotal part of daily tasks
- Complete and be accountable for accurate Quality and Due Diligence records
- Escalate quality or food safety concerns immediately to the appropriate level.
- Ensure that the correct product is packed
- Support the quality auditing process
- Take samples during and after production and carry out quality testing.
Shift pattern 4 days x 12 hours week 1, 4 nights x 12 hours week 2. 7am to 7pm or 7pm to 7am.
Requirements
- Experience in a retail/food manufacturing environment.
- Experience in quality assurance/quality control/ food safety/ environmental standards/ organics.
- Knowledge of Microsoft Office.
- Working experience within a similar role and/or a food environment.
- Awareness of the importance of food safety
Benefits
Some of our benefits include:
- Competitive Salary
- NEST Pension Scheme
- Annual Leave – 24.8 days
- Long service awards
- Employee Wellness Programmes
- Life Assurance
- Ride to Work Scheme
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Director of Quality Assurance
Posted 4 days ago
Job Viewed
Job Description
Position: Director of Quality Assurance & Regulatory Affairs
Location: Middlesex
Salary: 85K + benefits
Purpose of the Role
To lead global quality and regulatory strategy, ensuring compliance across the company's product portfolio. This role is pivotal in enabling market access, maintaining high standards, and embedding quality throughout the product lifecycle.
Strategic Leadership
- Represent role model or servant leader model leadership as a member of senior site management team.
- Develop and implement the QARA strategy aligned with business goals and regulatory compliance requirements.
- Collaborate with Engineering, Operations, and Commercial teams to integrate quality and compliance from concept to delivery.
- Represent the company in regulatory compliance audits and external engagements.
Regulatory Affairs
- Oversee global product registrations and submissions, including CE marking and international approvals for company products
- Support in defining regulatory pathways early in product development, including Intended Use and Risk Classification.
- Ensure compliance with ISO 13485, MDR, FDA 21 CFR Part 820, and other relevant standards.
Quality Assurance
- Maintain and enhance the Quality Management System (QMS).
- Lead internal and supplier audits, investigations, and corrective actions.
- Analyse QA data to drive continuous improvement and risk mitigation.
Project Oversight
- Lead QARA team in managing regulatory documentation and audit readiness.
- Support change control and post-market surveillance activities.
Team Development
- Mentor and develop QARA team members.
- Ensure training programmes reflect current regulatory and quality practices.
Skills & Experience
- Proven leadership in QARA within medical devices or regulated industries.
- Strong engineering background
- Experience with CE marking, Medical Device Requirements, both EU and UK, regulatory submissions, electrical safety requirements, software validation, and international compliance.
- Excellent communication and stakeholder engagement skills.
- Familiarity with electronic QMS and project management tools.
Desirable Qualifications
- Degree in Engineering, Life Sciences, or related field (Master's preferred).
- Experience working directly with regulatory bodies.
- Lead Auditor Certification
About Us
We are dedicated to fostering a diverse and inclusive community. In line with our Diversity and Inclusion policy, we welcome applications from all qualified individuals, regardless of age, gender, ethnicity, sexual orientation, or disability. As a Disability Confident Employer, and part of the Nicholas Associates Group, we are committed to supporting candidates with disabilities, and we're happy to discuss flexible working options.
We are committed to protecting the privacy of all our candidates and clients. If you choose to apply, your information will be processed in accordance with the Nicholas Associates Group of companies Privacy Notice.
Director of Quality Assurance
Posted 4 days ago
Job Viewed
Job Description
Position: Director of Quality Assurance & Regulatory Affairs
Location: Middlesex
Salary: 85K + benefits
Purpose of the Role
To lead global quality and regulatory strategy, ensuring compliance across the company's product portfolio. This role is pivotal in enabling market access, maintaining high standards, and embedding quality throughout the product lifecycle.
Strategic Leadership
- Represent role model or servant leader model leadership as a member of senior site management team.
- Develop and implement the QARA strategy aligned with business goals and regulatory compliance requirements.
- Collaborate with Engineering, Operations, and Commercial teams to integrate quality and compliance from concept to delivery.
- Represent the company in regulatory compliance audits and external engagements.
Regulatory Affairs
- Oversee global product registrations and submissions, including CE marking and international approvals for company products
- Support in defining regulatory pathways early in product development, including Intended Use and Risk Classification.
- Ensure compliance with ISO 13485, MDR, FDA 21 CFR Part 820, and other relevant standards.
Quality Assurance
- Maintain and enhance the Quality Management System (QMS).
- Lead internal and supplier audits, investigations, and corrective actions.
- Analyse QA data to drive continuous improvement and risk mitigation.
Project Oversight
- Lead QARA team in managing regulatory documentation and audit readiness.
- Support change control and post-market surveillance activities.
Team Development
- Mentor and develop QARA team members.
- Ensure training programmes reflect current regulatory and quality practices.
Skills & Experience
- Proven leadership in QARA within medical devices or regulated industries.
- Strong engineering background
- Experience with CE marking, Medical Device Requirements, both EU and UK, regulatory submissions, electrical safety requirements, software validation, and international compliance.
- Excellent communication and stakeholder engagement skills.
- Familiarity with electronic QMS and project management tools.
Desirable Qualifications
- Degree in Engineering, Life Sciences, or related field (Master's preferred).
- Experience working directly with regulatory bodies.
- Lead Auditor Certification
About Us
We are dedicated to fostering a diverse and inclusive community. In line with our Diversity and Inclusion policy, we welcome applications from all qualified individuals, regardless of age, gender, ethnicity, sexual orientation, or disability. As a Disability Confident Employer, and part of the Nicholas Associates Group, we are committed to supporting candidates with disabilities, and we're happy to discuss flexible working options.
We are committed to protecting the privacy of all our candidates and clients. If you choose to apply, your information will be processed in accordance with the Nicholas Associates Group of companies Privacy Notice.
Quality Control Technologist
Posted 2 days ago
Job Viewed
Job Description
Full Time | Permanent
Are you a skilled Quality Chemist that's looking to join a well reputed company that will invest in your future? We're working with a renowned manufacturer of coatings products who are looking for someone to come in and ensure their products continue to stay of the highest quality. If you have a passion for ensuring quality and want to work with a company that loves to reinvest in its employees, this is the job for you.
What You'll Be Doing
The roles primary focus will be on ensuring that all products produced by the company are up to their reputedly high standards. To do this you will be expected to undertake quality control testing of their manufactured products, support manufacturing and investigate customer feedback. You will also be expected to assist in the evaluations of raw materials and product development as requested.
What You'll Bring
Essential
- An A Level or equivalent qualification in Chemistry and/or Physics
- Previous analytical chemistry or quality control experience within an industrial laboratory
- Demonstrable technical ability and analytical skills
- The ability to work well both independently and as part of a team
- A full driving license
You can also send your CV through to Dylan Starling at: