1,292 Product Quality Engineer jobs in the United Kingdom

ABOUT ORGANOX:

OrganOx is an innovative, fast-paced, global medical device company with a mission to save lives by making every donated organ count. We are a commercial stage organ technology company, spun out of the University of Oxford in 2008, committed to improving transplantation outcomes throughout the world. The company’s first product, the OrganOx metra ® normothermic machine perfusion (NMP) system for liver transplantation, has been used to support more than 5,000 liver transplant operations globally.

Position Summary

The Product Quality Engineer oversees device inspection and acceptance activities for the OrganOx Metra, a Class III medical device. These activities include but are not limited to oversight of incoming inspection, nonconforming material and material review board, calibration and measurement systems, and product acceptance. This position works closely with contracted manufacturers and quality inspectors to ensure day to day execution of these critical business processes and lead improvements of these processes.

This position involves supervisory responsibilities of Quality Inspectors and technicians, as well as executing continuous improvement initiatives to improve product quality. This is an onsite position.

Listed below are the major responsibilities of the role and a brief description of some of the key tasks to be performed. This list is not totally exhaustive.

Major Responsibilities

Under direction from the Sr. Manager, Product Quality Engineering, the Product Quality Engineer may be responsible for:

• Leadership and Team Development
• Day to day management of quality inspectors and technicians
• Define team goals in collaboration with the Sr. Manager, Product Quality Engineering
• Manage performance reviews and development plans for quality inspectors and technicians
• Day to Day management and monitoring of KPIs related to product quality (Ex- Investigation Aging, NC aging and resolution)
• Promote a culture of accountability, collaboration and continuous improvement.

• Technical Quality Engineering Oversight

• Conducting hands on oversite of the device acceptance process, ensuring device acceptance targets are met.
• Conducting hands on oversight of the incoming inspection process, ensuring inspection targets are met.
• Conduct root cause investigations regarding non-conforming product
• Lead and support continuous process improvements related to device acceptance and incoming inspection
• Leading Material Review Board and dispositioning inspected product
• Execution of non-conformances
• Trending and analysis of non-conformance data to drive decisions
• Support updates to specification templates and inspection criteria 
• Support development of inspection fixtures and tooling
• Ensure calibration records are up to date
• Lead and support quality process improvements, identify systemic issues and drive continuous improvement initiatives

• Regulatory Compliance & QMS

• Ensure adherence to regulatory standards: FDA 21 CFR 820, ISO 13485, EU MDR, MDSAP, etc.
• Support regulatory submissions, internal audits, and external inspections (e.g., FDA, Notified Body).
• Maintain and improve quality processes and documentation within the QMS.
• Cross-Functional Collaboration
• Participate in Design Reviews and Change Control Boards.
• Collaborate with suppliers and contract manufacturers on quality standards, audits, and issue resolution.
• Communicate diligently with evidence-based communication to management and peers

•  Adhere to the letter and spirit of OrganOx’s Code of Conduct and all other company policies

Requirements

Skills & Experience

• 2-5  years of related quality engineering work experience within the medical device field or other highly regulated industry required
• Knowledge of regulatory and quality standards: FDA QSR, ISO 13485, ISO 14971, EU MDR. 
• Ability to travel internationally up to 30% to support contract manufacturers and suppliers, visit OrganOx sites, and visit customer sites
• Demonstrable technical quality engineering skills including root cause analysis, test method development, fixture development, and project management
• Experience working with nonconformances, CAPAs and SCARs
• Proven track record of problem solving and improving quality processes
• Experience with statistics and data analysis

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or a related technical field required
• ASQ Certifications (CQE, CMQ/OE, CQA) preferred 
• Six Sigma Green Belt or Black Belt Certification preferred

Benefits

At OrganOx, we value innovation, evidence, integrity, teamwork, respect, and passion. We offer competitive compensation and comprehensive benefits, including healthcare and retirement plans. We support work-life balance and provide opportunities for ongoing professional development.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to age, disability, gender reassignment, marriage and civil partnership, pregnancy and maternity, race, religion or belief, sex, sexual orientation race, or any other characteristics protected by law.

We are seeking a highly motivated and results-oriented Product Quality Engineer to join our dynamic team. In this critical role,

you will be responsible for ensuring the highest quality standards throughout concept to production. You will play a key role in

identifying and mitigating potential quality issues, driving continuous improvement initiatives, and ensuring customer

satisfaction.

● Drawing Quality Checks & Sign-off: Review and approve engineering drawings, ensuring accuracy, completeness, tolerance

analysis and compliance with industry standards.

● Process & Production Design: Participate in the development and optimisation of manufacturing processes, including

production line layouts, assembly methods, and tooling.

● Quality Control: Implement and monitor robust quality control systems, including inspection procedures, sampling plans,

release criteria and statistical process control (SPC) techniques with cpk/ppk

● Product Quality Audits: Conduct regular internal and external quality audits to assess product conformance and identify

areas for improvement to ISO9001

● FMEA Analysis: Conduct thorough Failure Mode and Effects Analysis (FMEA), including Design FMEA (DFMEA) and Process

FMEA (PFMEA), to proactively identify and mitigate potential risks and failures.

● Design for Manufacturing & Assembly (DFM/DFA): Collaborate closely with the design and engineering teams to ensure

products are designed for optimal manufacturability and assembly.

● Measuring Reports: Generate and analyse measuring reports, MSAs, ensuring alignment with engineering drawings and

specifications.

● Document Review Reports: Conduct thorough reviews of all relevant documentation, including work instructions, procedures,

and quality plans connected to the NPD process.

● Process Jigs & Fixtures Ownership: Oversee the design, development, and maintenance of jigs, fixtures, and other production

tooling.

● Part & Assembly Quality Accountability: Ensure the quality of all parts and assemblies throughout the production process,

from raw materials to finished goods.

● Work Instructions: Develop and maintain clear and concise work instructions that align with product drawings and

specifications.

● Production & Assembly Line Process Qualification: Participate in the qualification of new production lines and assembly

processes, ensuring they meet all performance and quality requirements.

Requirements

Qualifications:

● Bachelor's degree in Mechanical Engineering, Industrial Engineering, or a related field.

Skills & Experience:

● 3+ years of experience as a Quality Engineer in a manufacturing environment.

● Strong understanding of quality management systems, including ISO 9001.

● Proficiency in FMEA, DFM/DFA, and other quality engineering tools and methodologies.

● Experience with GD&T (Geometric Dimensioning and Tolerancing).

● Excellent analytical, problem-solving, and communication skills.

● Strong attention to detail and a results-oriented approach.

● Experience with ERP and/or PLM systems is a plus.

Benefits

• Competitive salary and bonus scheme
• Hybrid working
• Rentokil Initial Reward Scheme
• 23 days holiday, plus 8 bank holidays
• Employee Assistance Programme
• Death in service benefit
• Healthcare
• Free parking

At Rentokil Initial, our customers and colleagues represent diverse backgrounds and experiences. We take pride in being an equal opportunity employer, actively encouraging applications from individuals from all walks of life. Our belief is that everyone irrespective of age, gender, gender identity, gender expression, ethnicity, sexual orientation, disabilities, religion, or beliefs, has the potential to thrive and contribute.

We embrace the differences that make each of our colleagues unique, fostering an inclusive environment where everyone can be their authentic selves and feel a sense of belonging. To ensure that your journey with us is accessible if you have any individual requirements we invite you to communicate any specific needs or preferences you may have during any stage of the recruitment process. Our team is available to support you; feel free to reach out to ( ) if you need anything

Be Yourself in Your Application! At Rentokil Initial, we value innovation, but we want to see the real you! While AI can help with structure and grammar, make sure your application shows your true passion and understanding of the role. A personal touch will help you stand out. 

• Quality Management System (QMS) Oversight:
• Develop, implement, and maintain quality management systems in line with ISO 9001 and ISO 14001 standards.
• Conduct internal audits and facilitate external audits to ensure ongoing compliance and identify areas for improvement.
• Manage and update quality documentation, procedures, and records.

• Create comprehensive system reports for General Administration (GA) purposes using Microsoft Package tools.
• Analyze data to identify trends, root causes of non-conformities, and opportunities for process optimization.
• Present findings and recommendations to management.

• Manage and oversee compliance with established management systems for ISO 9001 and ISO 14001.
• Demonstrate knowledge or experience with British Retail Consortium (BRC) standards.
• Possess knowledge or experience with Forest Stewardship Council (FSC) principles and standards.

• Assist in the planning and implementation of data security protocols and best practices to protect sensitive company information.

• Undertake various administrative tasks as required to support the smooth running of the department and wider business operations.

• Experience: 2-3 years of experience upwards in a Quality Assurance or similar role.
• Technical Skills: Proficient in Microsoft Package (e.g., Word, Excel, PowerPoint) for reporting and data management.
• Industry Knowledge: Proven experience with ISO 9001 and ISO 14001 management systems.
• Desirable: Experience or knowledge of BRC (British Retail Consortium) and FSC (Forest Stewardship Council) standards.
• Advantageous: Previous experience within the food industry.
• Personal Attributes: Highly organised, meticulous attention to detail, excellent communication skills, and ability to work independently and as part of a team.

• Monday to Friday, 9am - 6pm

• 30,000 - 40,000 per annum, depending on experience

• Annual Salary: 12.50 per hour
• Location: Enfield
• Job Type: Permanent

We are seeking a QA/QC Lab Assistant to join our team on a permanent basis. This role is ideal for candidates who are excellent communicators, hard workers, and effective team players. Experience in Food Manufacturing is not required, making this a great opportunity for those looking to enter the field.

• Actively participate in the QC (Lab) Department.
• Assist in maintaining factory standards to ensure compliance with Food Safety Standards and company processes.
• Work collaboratively within the team to support various lab functions and projects.

• No previous experience in Food Manufacturing necessary.
• Strong communication skills.
• Ability to work effectively both independently and as part of a team.
• Commitment to maintaining high quality and safety standards.

• Monday - Friday (37.5-hour week).
• Shift patterns include:
  • 6am-2pm
  • 7am-3pm
  • 8am-4pm
  • 9.30am-5.30pm

• Competitive salary.
• Stable employment with a structured work schedule.
• Opportunity to develop skills in a supportive environment.

To apply for the QA/QC Lab Assistant position, please submit your CV and cover letter detailing your interest in the role and any relevant skills or experiences. Apply today for an immediate start!

Quality Assurance Engineer - Manufacturing | Bolton

Join a cutting-edge manufacturing environment where your expertise in quality assurance will directly impact high-profile engineering projects. We're looking for a proactive QA Engineer to support and improve manufacturing processes across multiple UK sites.

What you'll be doing:

• Drive quality excellence across manufacturing programmes

• Lead audits, risk assessments, and non-conformance investigations

• Influence continuous improvement and ensure compliance with industry standards

• Collaborate with cross-functional teams to deliver projects on time, to cost, and at high quality

What you'll bring:

• HNC/HND or equivalent in a relevant subject

• Strong experience in quality assurance within engineering/manufacturing

• Solid knowledge of EN9100/AS9100 and auditing practices

• Confident using problem-solving tools (8D, 5Y, PFMEA)

• Great communication skills and a drive to make real impact

Ready to shape the future of manufacturing quality? Apply now and help drive world-class performance.

• Quality Management System (QMS) Oversight:
• Develop, implement, and maintain quality management systems in line with ISO 9001 and ISO 14001 standards.
• Conduct internal audits and facilitate external audits to ensure ongoing compliance and identify areas for improvement.
• Manage and update quality documentation, procedures, and records.

• Create comprehensive system reports for General Administration (GA) purposes using Microsoft Package tools.
• Analyze data to identify trends, root causes of non-conformities, and opportunities for process optimization.
• Present findings and recommendations to management.

• Manage and oversee compliance with established management systems for ISO 9001 and ISO 14001.
• Demonstrate knowledge or experience with British Retail Consortium (BRC) standards.
• Possess knowledge or experience with Forest Stewardship Council (FSC) principles and standards.

• Assist in the planning and implementation of data security protocols and best practices to protect sensitive company information.

• Undertake various administrative tasks as required to support the smooth running of the department and wider business operations.

• Experience: 2-3 years of experience upwards in a Quality Assurance or similar role.
• Technical Skills: Proficient in Microsoft Package (e.g., Word, Excel, PowerPoint) for reporting and data management.
• Industry Knowledge: Proven experience with ISO 9001 and ISO 14001 management systems.
• Desirable: Experience or knowledge of BRC (British Retail Consortium) and FSC (Forest Stewardship Council) standards.
• Advantageous: Previous experience within the food industry.
• Personal Attributes: Highly organised, meticulous attention to detail, excellent communication skills, and ability to work independently and as part of a team.

• Monday to Friday, 9am - 6pm

• 30,000 - 40,000 per annum, depending on experience

Quality Assurance Engineer - Manufacturing | Bolton

Join a cutting-edge manufacturing environment where your expertise in quality assurance will directly impact high-profile engineering projects. We're looking for a proactive QA Engineer to support and improve manufacturing processes across multiple UK sites.

What you'll be doing:

• Drive quality excellence across manufacturing programmes

• Lead audits, risk assessments, and non-conformance investigations

• Influence continuous improvement and ensure compliance with industry standards

• Collaborate with cross-functional teams to deliver projects on time, to cost, and at high quality

What you'll bring:

• HNC/HND or equivalent in a relevant subject

• Strong experience in quality assurance within engineering/manufacturing

• Solid knowledge of EN9100/AS9100 and auditing practices

• Confident using problem-solving tools (8D, 5Y, PFMEA)

• Great communication skills and a drive to make real impact

Ready to shape the future of manufacturing quality? Apply now and help drive world-class performance.

• Annual Salary: 12.50 per hour
• Location: Enfield
• Job Type: Permanent

We are seeking a QA/QC Lab Assistant to join our team on a permanent basis. This role is ideal for candidates who are excellent communicators, hard workers, and effective team players. Experience in Food Manufacturing is not required, making this a great opportunity for those looking to enter the field.

• Actively participate in the QC (Lab) Department.
• Assist in maintaining factory standards to ensure compliance with Food Safety Standards and company processes.
• Work collaboratively within the team to support various lab functions and projects.

• No previous experience in Food Manufacturing necessary.
• Strong communication skills.
• Ability to work effectively both independently and as part of a team.
• Commitment to maintaining high quality and safety standards.

• Monday - Friday (37.5-hour week).
• Shift patterns include:
  • 6am-2pm
  • 7am-3pm
  • 8am-4pm
  • 9.30am-5.30pm

• Competitive salary.
• Stable employment with a structured work schedule.
• Opportunity to develop skills in a supportive environment.

To apply for the QA/QC Lab Assistant position, please submit your CV and cover letter detailing your interest in the role and any relevant skills or experiences. Apply today for an immediate start!