Explore opportunities in quality management, a field focused on maintaining standards and continuous improvement. Quality management jobs are available across various industries, from manufacturing to healthcare, playing a crucial role in ensuring products and services meet customer expectations and regulatory requirements. Professionals in this area work on process optimization, data analysis, and implementing quality control systems.16 Quality Management jobs in the United Kingdom
Quality Assurance Manager - Oxford
Posted 2 days ago
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Job Description
We are seeking a highly focused and experienced Quality Assurance Manager to actively lead on the implementation of clinical governance and assurance frameworks within the centre. This position will play a pivotal role in overseeing quality assurance and ensuring that compliance with all healthcare regulatory requirements is embedded in both clinical and non-clinical teams across our unique, private patient day-case centre and in the on-going development of our world class patient care. We require an individual who can ensure that the best practice standards become part of the day-to-day business for the Welbeck centre, through collaboration, partnership and close working relationships with centre leadership and core teams.
- Location: Oxford
- Full Time
Job Responsibilities
You will work predominantly Monday-Friday around the core hours of 9-6pm, however will need to be flexible to meet the needs of the centre which has extended opening hours and potential for weekend services. This position as Quality Assurance Manager is a senior managerial position, promoting clinical leadership through all aspects of the role by initiating optimal clinical standards, and facilitating effective communications with clinicians and teams. You will be creating, applying and monitoring governance systems to ensure the implementation of the Welbeck Quality Assurance and Governance Strategy. This role is line managed by the Clinical Services Director but has a close working relationship with the Registered Manager for the centre, as well as working with the Welbeck Health Group Chief Clinical Officer, Clinical Quality Team and Subject Matter Experts (SMEs) to implement specific projects for compliance and improvement.
Leadership, Engagement and Education
• Promote and embed a culture of informed questioning, challenge, trend analysis and information triangulation to ensure lessons are learned
• Champion the benefits of clinical governance, providing training and support to staff at all levels on governance processes and quality improvement
• Facilitate the provision of trend data and benchmarking insights to drive innovation and share best practice across departments
Quality Assurance and Governance
• Lead and co-ordinate the centre’s clinical governance and quality assurance programmes to ensure safe and high-quality patient care
• Review and analyse quality, safety, and governance data, using Welbeck systems to identify trends, and deliver improvement actions
• Produce high-quality governance reports for the Quality Assurance Performance Improvement Committee and other governance committees
Regulatory Compliance and Risk Management
• Support the centre in achieving and maintaining a ‘Good’ or higher rating in regulatory inspections
• Prepare the centre for CQC inspections, working proactively with department leads to ensure readiness to demonstrate compliance
• Co-ordinate action plans in response to external inspections and audits, ensuring timely implementation and monitoring of improvements
Incident and Complaint Management
• Manage the complaints process, ensuring that all complaints are investigated and appropriately closed with a focus on learning and resolution
• Support Patient Safety Incident Investigations (PSII), contributing to or leading investigations using tools such as Root Cause Analysis
• Ensure that incidents are reported, analysed, and closed appropriately, and that learning is shared across the centre and the wider Welbeck group
Data and Evidence Management
• Ensure robust data collection systems are in place to monitor compliance with national policies and internal standards
• Provide timely, accurate quality data and insights to support strategic objectives and operational decision-making
• Work with clinical teams to ensure centre wide audit cycles are completed, and results are acted upon to improve patient care and outcomes
Experience / Qualifications
Essential
• Registered nurse or AHP with valid NMC or HCPC registration
• Knowledge of the components of quality governance including risk management
• Experience in working in quality governance in a healthcare environment
• Have experience of CQC inspections and/or readiness
• Must have excellent report and letter writing skills, alongside good IT skills including Excel and PowerPoint presentations
• Demonstrable strong communication skills, with a range of individuals
• Must have evidence of developing successful partnership working and implementing change
• Show compassionate and drive by being able to showcase excellent patient care
• Be able to utilise your leadership skills to demonstrate and implement clinical best practice
• The successful candidate will be able to demonstrate excellence in:
o Leadership & people management skills – ability to think and plan strategically and tactically
o Adaptability and agility - flexibility in approach and attitude
o Communications skills – presenting, influencing, persuading and negotiating with a range of stakeholders
o Collaboration – building partnerships and strategic working relationships
o Integrity and resilience – focused on high standards and able to support and enable others to do the same
o Problem solving skills – able to analyse complex problems and implement practical workable solutions
o Planning, organisation and delegation skills – highly developed to prioritise competing work demands
Desirable
• Experience of private healthcare market
• Experience in quality improvement, benchmarking, and project facilitation
• Strong analytical and reporting skills with the ability to interpret complex data and translate findings into actions
• Knowledge of national quality initiatives, patient safety strategies, and current healthcare regulatory developments
• Familiarity with governance and incident reporting platforms used in private or NHS settings
Quality Management Lead
Posted 2 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 Consultant - ISO
Posted today
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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.
Quality Management Consultant - ISO
Posted today
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Job Description
A variety of soft skills and experience may be required for the following role Please ensure you check the overview below carefully.
Please click on the apply button to read the full job description
Quality Management Systems (QMS) Specialist
Posted 3 days ago
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Job Description
Baltic Recruitment are currently recruiting for a Quality Management Systems (QMS) Specialist joining a highly reputable client based in Sunderland. This is Temporary Contract - 12 Months.
Our Client is a force for innovation, growth, and transformation. Who does things differently and does them with purpose. Their success is built by passionate people who challenge the status quo, and now, they're looking for you to join them.
We're on the hunt for a Quality Management Systems (QMS) Specialist to join their dynamic Quality team. This is your opportunity to be part of a forward-thinking, collaborative environment where your ideas and expertise will directly influence our success.
Main assignment:
As the QMS specialist you are responsible for ensuring our business is fully compliant with the Company's Quality Management System (QMS), and certified management systems and standards. You will work to ensure compliance through auditing, stakeholder engagement, driving continuous improvement activities and leading in the system development. In addition, you will be accountable for day-to-day management of Shift Quality. Ensuring smooth running of quality to support business objectives & KPI achievement. Promoting standardisation of best practice and continuous improvement between shifts to ensure a consistent approach across shifts.
Summary of Main Duties and Responsibilities:
- Day to day management of shift quality team
- Coordinating activities relating to our Business Management Systems (BMS)
- Being the business system liaison for all departments
- Working closely with internal and external stakeholders, being the key point of contact for a range of third parties assessing our BMS'
- Creating, implementing and monitoring audit schedules
- Leading the prioritisation and close out of internal audits
- Developing and leading the compliance and improvement management plan(s)
- Proactively monitoring overdue compliance actions to ensure completion
- Plan and attend audit opening and closing meetings, and co-ordinate responses to audit findings
- Establish and maintain records of all audits, including any findings raised, whilst also ensuring any findings are closed out with notification from the auditor.
- Communicate changes to the BMS, along with advice on their implications to working practices.
- The efficient preparation and management of business system documentation (creation, categorising, storing, updating, archiving and retrieval)
- Group Level auditing IATF 16949 ISO 14000
QMS Specialist Applicants:
- Strong leadership skills with a proven track record of leading teams and engaging stakeholder
- Methodical approach and detailed orientated
- Ability to influence and negotiate
- Excellent level of communication skills
Company Benefits:
Because our Client don't just offer jobs - they offer careers. Within this role, you'll work in a stimulating, supportive atmosphere that pushes boundaries and encourages growth. Their benefits package reflects their commitment to your well-being and includes:
- Life Assurance & Income Protection Insurance
- Critical Illness & Private Medical Cover
- Dental & Optical Insurance
- Group Pension Scheme
- Cycle to Work Scheme
- Overtime Pay
- Buy & Sell Holiday Options
And yes, you'll enjoy early finishes every Friday !
Working Hours:
Monday - Thursday: 7:55am - 4:30pm
Friday: 7:55am - 2:15pm (start your weekend early!)
If you're looking for your next challenge - where your skills will be valued, your ideas welcomed, and your growth supported - then we want to hear from you. Join the team and shape the future with them!
Quality Management Systems (QMS) Specialist
Posted 2 days ago
Job Viewed
Job Description
Baltic Recruitment are currently recruiting for a Quality Management Systems (QMS) Specialist joining a highly reputable client based in Sunderland. This is Temporary Contract - 12 Months.
Our Client is a force for innovation, growth, and transformation. Who does things differently and does them with purpose. Their success is built by passionate people who challenge the status quo, and now, they're looking for you to join them.
We're on the hunt for a Quality Management Systems (QMS) Specialist to join their dynamic Quality team. This is your opportunity to be part of a forward-thinking, collaborative environment where your ideas and expertise will directly influence our success.
Main assignment:
As the QMS specialist you are responsible for ensuring our business is fully compliant with the Company's Quality Management System (QMS), and certified management systems and standards. You will work to ensure compliance through auditing, stakeholder engagement, driving continuous improvement activities and leading in the system development. In addition, you will be accountable for day-to-day management of Shift Quality. Ensuring smooth running of quality to support business objectives & KPI achievement. Promoting standardisation of best practice and continuous improvement between shifts to ensure a consistent approach across shifts.
Summary of Main Duties and Responsibilities:
- Day to day management of shift quality team
- Coordinating activities relating to our Business Management Systems (BMS)
- Being the business system liaison for all departments
- Working closely with internal and external stakeholders, being the key point of contact for a range of third parties assessing our BMS'
- Creating, implementing and monitoring audit schedules
- Leading the prioritisation and close out of internal audits
- Developing and leading the compliance and improvement management plan(s)
- Proactively monitoring overdue compliance actions to ensure completion
- Plan and attend audit opening and closing meetings, and co-ordinate responses to audit findings
- Establish and maintain records of all audits, including any findings raised, whilst also ensuring any findings are closed out with notification from the auditor.
- Communicate changes to the BMS, along with advice on their implications to working practices.
- The efficient preparation and management of business system documentation (creation, categorising, storing, updating, archiving and retrieval)
- Group Level auditing IATF 16949 ISO 14000
QMS Specialist Applicants:
- Strong leadership skills with a proven track record of leading teams and engaging stakeholder
- Methodical approach and detailed orientated
- Ability to influence and negotiate
- Excellent level of communication skills
Company Benefits:
Because our Client don't just offer jobs - they offer careers. Within this role, you'll work in a stimulating, supportive atmosphere that pushes boundaries and encourages growth. Their benefits package reflects their commitment to your well-being and includes:
- Life Assurance & Income Protection Insurance
- Critical Illness & Private Medical Cover
- Dental & Optical Insurance
- Group Pension Scheme
- Cycle to Work Scheme
- Overtime Pay
- Buy & Sell Holiday Options
And yes, you'll enjoy early finishes every Friday !
Working Hours:
Monday - Thursday: 7:55am - 4:30pm
Friday: 7:55am - 2:15pm (start your weekend early!)
If you're looking for your next challenge - where your skills will be valued, your ideas welcomed, and your growth supported - then we want to hear from you. Join the team and shape the future with them!
Senior Associate - Water Quality Management
Posted today
Job Viewed
Job Description
Senior Associate Consultant - Water Quality Management
Join our client’s established Environmental Consulting team as a Senior Associate Water Quality consultant. Lead strategic the Water Quality unit by leading on programs and collaborating with specialists in environmental impact assessment and hydro-ecology.
Proven experience in technical leadership, business growth and project execution. You will partner with utility companies, environmental agencies, and construction firms to identify water quality challenges and deliver science-based recommendations.
Key Requirements
- Extensive background in water assessment and program management
- Proven success managing large-scale environmental monitoring initiatives
- Strong relationship-building abilities with external partners
- Team leadership or mentoring experience across technical disciplines
- Business-focused mindset with budget management skills
The position will be for an Associate level to Associate Director level consultant – with a full remote working flexibility!
Depending on seniority, salary will vary between £60,000 to £70,000 per annum
If you are interested, please click apply or contact Jo Le Corre
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Senior Associate - Water Quality Management
Posted 7 days ago
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Job Description
br>Full remote option
Join our client’s established Environmental Consulting team as a Senior Associate Water Quality consultant. Lead strategic the Water Quality unit by leading on programs and collaborating with specialists in environmental impact assessment and hydro-ecology. < r>
Proven experience in technical leadership, business growth and project execution. You will partner with utility companies, environmental agencies, and construction firms to identify water quality challenges and deliver science-based recommendations.
Key Requirements
* Extensive background in water assessment and program management
* Proven success managing large-scale environmental monitoring initiatives
* Strong relationship-building abilities with external partners
* Team leadership or mentoring experience across technical disciplines
* Business-focused mindset with budget management skills
The position will be for an Associate level to Associate Director level consultant – with a full remote working flexibility! < r>
Depending on seniority, salary will vary between �60,000 to �70,000 per annum
Sr Dir GD Quality Management (GVP)
Posted 1 day 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 1 day ago
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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