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Quality Coordinator

Last updated: 2026/02/10 at 9:40 PM
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6 Min Read
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  • Permanent
  • United Kingdom
  • Posted 3 weeks ago
CV-Library

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Quality Coordinator

Summary:

The Quality Coordinator for Nijhuis Saur Industries in Stoke is responsible for ensuring the laboratory and Riventa business unit operate to the highest quality standards by managing accreditation compliance, internal and external audits, QA/QC processes, instrument calibration, data analysis, and documentation control. The role provides technical guidance to staff, supports method development, oversees customer satisfaction and performance metrics, leads accreditation audit representation, and manages non‑conformance investigations. It also involves collaborating with management and customers, producing performance reports, supporting routine and specialised testing, and maintaining ISO 9001 and ISO 17025 quality systems for both laboratory and manufactured parts environments.

Duties and Responsibilities:

• Ensure compliance with laboratory accreditation, regulatory standards and provide guidance to staff to ensure that quality policies, processes and procedures are established, current and adhered to by all laboratory staff.

• Oversee laboratory internal audit processes, external proficiency testing programs, document control systems, competency assessment, training, and other quality processes.

• Support the development of instrument techniques, ensuring adequate calibrations and QC are in place.

• Monitor customer satisfaction and performance metrics of the laboratory.

• Liaise with management throughout the business as well as customers when reporting on quality and statistical data.

• Oversee the Riventa business unit quality system including manufactured parts QA/QC process, calibration of temperature probes to approved methods, warranty, repair and returns process for Riventa parts.

• Maintain a quality management system for Riventa

• Work to the global NSI ISO 9001 accredited quality management system.

• Work to the NSI WTL ISO 17025 accredited quality management system.

• Manage, document and audit the Riventa incoming and assembled products/parts testing and acceptance QA/QC process at the Stoke facility, in collaboration with the Riventa team.

• Manage, document and audit the Riventa temperature and pressure probe calibration process to relevant standards.

• Conduct lab testing to high standards through busy periods or during periods of absence of Laboratory Analyst or Develop Analysts.

• Audit the analytical performance of the analysts, content of laboratory methodology and documentation to ensure compliance with the quality system.

• Represent the laboratory during annual accreditation audits.

• Oversee the laboratories non-conformance log to ensure its appropriate use and investigations are completed in full, with appropriate actions.

• Analyse data, identify trends, monitor prevention and correction of quality deviations, and develop reports for management utilising regulatory knowledge, technical knowledge and laboratory experience.

• To provide quality support to the laboratory for routine testing when required as well as providing quality support to the Technical Development Scientist and the wider technical team with specialised testing and the growth of these methods.

• Report periodically to management, customers on the quality performance of the laboratory.

• Presenting data to stakeholders on laboratory performance statistics.

• Support the creation and reviewing of validation reports for new and current tests.

• Perform Uncertainty of Measurement calculations when required.

• This is not a fully comprehensive list of responsibilities, and other duties will be expected to be completed within the limits of the position.

Working for us means: 

The salary is between £33,000 & £38,000 per year, depending on your professional experience.

Hours of Work – 40 hours per week, Monday to Friday 

Overtime – will be paid at 1.5.  (Not applicable for Manager and Coordinator role)

Holidays – 25 days + 8 statutory days (pro-rata)

Probationary Period – 6 months.

Pension – Can join immediately or auto enrolled after 3 months – Employee 5% and Employer 5% via salary sacrifice.

Eligible to join Private Healthcare after successfully completing probation.

Enrolled in Group Income Protection and Death in Service (4 x basic salary) upon commencement of employment.

Notice – 1 Month during probation, increasing to 3 months thereafter.

Nijhuis Saur Industries UK & Ireland are committed to maintaining Environmental & Social Impact goals:

To reach Net Zero emissions across our value chain by 2040.
To continuously meet high standards of social and environmental performance, transparency, accountability, maintaining B-Corp Certification.
To be a socially responsible company creating a positive impact to all stakeholders including workers, communities, customers, and our planet.

Nijhuis Saur Industries UK & Ireland are an equal opportunity employer; we are committed to providing equal opportunities in all aspects of employment in line with the Equality Act 2010.

Are you a recruiter?

Please do not call or email us unless we have contacted you first. We believe that we can find our new colleagues ourselves, therefore agency support is not desired. Profiles and resumes sent unsolicited by agencies, even if you send them directly to a hiring manager, will be treated as direct applications from the candidate.

Join our #missionwater

 

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