898 Quality Management Systems jobs in the United Kingdom
Quality Management Systems (QMS) Specialist
Posted 4 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!
Quality Management Systems (QMS) Specialist
Posted 4 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!
Quality Management Systems Sr Specialist, CAPA-Medical Devices
Posted 3 days ago
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
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
Quality Control Technologist
Posted 3 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:
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Production - Quality Control
Posted 4 days ago
Job Viewed
Job Description
Production / Quality Control Operative
Hourly Rate: £12.21 – £3.21
Location: Liskeard
Job Type: Full-time
Hours: Monday to Friday
- Shift 1: 06:00 – 14:00
- Shift 2: 14:00 – 22:00
We are looking for a reliable and detail-oriented Production / Quality Control Operative to join our team. This role involves working across production and quality control functions to ensure products meet company standards and customer expectations.
Key Responsibilities:- Operate machinery and equipment safely and efficiently
- Package products according to specifications
- Conduct quality checks throughout the production process
- Maintain accurate records of production and quality data
- Ensure compliance with hygiene and safety standards
- Report any issues or defects to the supervisor promptly
- Support continuous improvement initiatives
- Maintain a clean and organised work environment
- Good attention to detail and commitment to quality
- Ability to follow procedures and work independently
- Strong communication and teamwork skills
- Willingness to work rotating shifts
- Basic understanding of production processes and quality control
- Previous experience in a food production or manufacturing environment
- Familiarity with quality control procedures
- Basic computer skills (e.g., Excel)
- Understanding of health & safety and hygiene standards
- Competitive hourly rate (£12.21 – £1 21)
- Ongoing training and development
- Opportunities for progression
- Supportive team environment
- Company pension scheme
- Free on-site parking
Please send your CV and a brief cover letter to (url removed) or call Sarah on (phone number removed).
Quality Control Inspector
Posted 4 days ago
Job Viewed
Job Description
The Recruitment Group is looking for an experienced Quality Control Inspector who has got a background in Quality and Aerospace. Our Client has over 40 years of experience in their field and is looking for a Quality Control Inspector to join their fast-paced and friendly quality and inspection team. If you feel that the role of Quality Control Inspector could be for you, then please read below:
Pay for the Quality Control Inspector: £14.00 per hour
Shifts:
- Monday to Thursday – 7am to 4pm
- Friday – 7am to 1pm
- 30 minutes unpaid lunch break
Role Responsibilities:
- Understanding of AS9100 standards
- Visual inspection of components to a quality standard using various inspection methods
- Ability to read customer drawings & understand specifications
- Support with inspection reports
- Investigate any rejects and non-conformance parts
- Work with various departments regarding the processing of inspection
- Previous experience within a similar role is essential
About You:
- Previous experience of aerospace inspection
- Good attention-to-detail and care is required
- Good organisational abilities
- Enthusiasm to develop your skills and knowledge
- Ability to work unsupervised and deliver quality work
- Excellent work ethics and communication
For more information and to apply, get in touch with Jane at our Loughborough Branch to submit your application.
If you would like to know how we will store and process your data, please visit The Recruitment Group's home page to read our GDPR Data Protection
Quality Control Microbiologist
Posted 4 days ago
Job Viewed
Job Description
STEM Recruitment Solutions is seeking a Senior Quality Control Technician/ Microbiologist for our client based in Perthshire, Scotland.
This will initially be a 6 month contract with the potential to go permanent for the right candidate and if business needs allow. The main job responsibilities of the candidate will be:
- Collect and process samples ready for testing.
- Perform pH testing and microbiological testing of samples.
- Microbiological testing in strict accordance with the ISO 17025 & 13485/9001 Quality Management Systems and Quality Policies.
- Report non-conforming results to the QC Team Leader or Quality Manager meticulously.
- In-depth knowledge of ISO 17025 testing procedures.
- Proficiency in aseptic technique and fundamental pipetting techniques.
- Experience with contamination checks, pH, conductivity, membrane filtration, and media fertility testing.
The ideal candidate will have as a minimum a BSc in Microbiology or other related field, or equivalent experience. Demonstrated experience working in a laboratory environment is advantageous but the position would also suit a recent graduate with the relevant skills.
Our client offers competitive contract rates, a supportive work environment, and opportunities for professional development within the biotechnology sector. This role is ideal for candidates eager to utilise their microbiology expertise in a vital QC function, contributing to innovative research and product quality assurance.
As this is a short term contract role preference will be given to candidates readily available to commute to site.
Please apply online in the first instance or for more information contract Alex at STEM.