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Quality Manager

BluetownOnline Ltd
Posted 2 days ago, valid for a month
Location

Tewkesbury, Gloucestershire GL20, England

Salary

£45,000 per annum

Contract type

Full Time

In order to submit this application, a TotalJobs account will be created for you. As such, in addition to applying for this job, you will be signed up to all TotalJobs’ services as part of the process. By submitting this application, you agree to TotalJobs’ Terms and Conditions and acknowledge that your personal data will be transferred to TotalJobs and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • The Quality Manager position in Tewkesbury offers a competitive salary ranging from £40,000 to £45,000.
  • This is a full-time permanent role, although part-time options may be available for the right candidate.
  • The ideal applicant should have experience in a regulated manufacturing environment, particularly in sectors like Med Device, Pharma, or aerospace.
  • Candidates must possess a solid understanding of ISO 9001 and have experience conducting internal and external audits.
  • Relevant job titles for consideration include Quality Assurance Manager, Quality Control Manager, and Director of Quality.

Job Title: Quality Manager

Location: Tewkesbury

Salary: £40K - £45K

Job Type: Full time, though part time considered for the right candidate / Permanent

About Us:

The Company are now recruiting for a Quality Manager on a permanent basis. This critical role is at the heart of ensuring quality and compliance, taking ownership of QA and QMS across our site. The role offers a competitive salary of £40,000 - £45,000 plus benefits. This is a full-time position although we may consider a reduced hours contract for the right candidate.

About the role:

As a Quality Manager, you will play an integral role in maintaining the high standards of our customer requirements with a focus on implementing, maintaining and improving ISO certifications. You'll be responsible for the Quality Management Systems (QMS) driving continual improvement in quality standards while also planning and implementing internal and external quality audits. You will ensure that all documentation is in place for raw materials, semi-finished goods and finished goods to comply with agreed specifications and supporting the management oversee the safety of the laboratory and accuracy of documentation methods and calibrations. As Quality Manager, part of your responsibility is to support investigations into non-conforming products both internally and at suppliers' end, as well as dealing with customer complaints promptly and implementing corrective action processes.

Duties and Responsibilities:

  • Implement, maintain and improve ISO 9001 and ISO 13485 certifications.
  • Responsible for the Quality Management System (QMS).
  • Plan, implement and drive internal and external quality audits.
  • Ensure that all documentation is in place to ensure that raw material, semi-finished goods and finished goods are compliant with agreed specifications.
  • Responsible for team supervision, documentation methods, calibration.
  • Support investigation to non-conforming product (internal manufacturing and at supplier's). Ensuring customer complaints are dealt with in a timely manner and implement corrective action process.
  • Provide escalation, weekly updates and reports.
  • Take personal responsibility for the notification and tracking of quality activities and related database entry/data accuracy.

About you:

The ideal candidate for the Quality Manager role will bring a wealth of experience from working in a manufacturing or production environment with a background within a regulated setting such as Med Device, Pharma or aerospace. You will have a solid understanding and experience of ISO 9001, while knowledge of other standards such as ISO14001, ISO45001 and ISO13485 would also be advantageous. Your experience conducting internal and external audits will be crucial to your success in this role, so your application should demonstrate auditor training or qualifications.

  • Engineering Degree or Proven experience
  • Experience of working in a regulated manufacturing / production environment
  • Knowledge and experience of ISO 9001
  • Experience of conducting internal and external audits
  • Experience of working with Medical devices is desirable
  • Knowledge of other standards such as ISO14001, ISO45001 and ISO13485 would be an advantage

Please click the APPLY button to submit your CV for this role

Candidates with experience or relevant job titles of Quality Assurance Manager, Quality Control Manager, Director of Quality, Quality Improvement Manager, and Head of Quality Assurance may also be considered.

Apply now in a few quick clicks

In order to submit this application, a TotalJobs account will be created for you. As such, in addition to applying for this job, you will be signed up to all TotalJobs’ services as part of the process. By submitting this application, you agree to TotalJobs’ Terms and Conditions and acknowledge that your personal data will be transferred to TotalJobs and processed by them in accordance with their Privacy Policy.