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Quality Assurance Manager

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Stoke-on-Trent

On-site

GBP 80,000 - 100,000

Full time

21 days ago

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Job summary

An international advanced pharmaceutical and medical device company is seeking a QA Manager to lead quality assurance activities across critical sites in the UK. This hands-on role involves managing a small team, overseeing quality systems, and ensuring compliance in a GMP environment. Ideal candidates will have strong leadership skills and experience in auditing and validation activities. This is a unique opportunity to make a significant impact on quality assurance practices and contribute to the company’s operational excellence. If you are passionate about quality and looking to advance your career, this position is for you.

Qualifications

  • Experience in a QA role within a GMP environment is essential.
  • Leadership skills and hands-on coaching experience are crucial.

Responsibilities

  • Manage a small team and oversee quality systems and operational delivery.
  • Lead through hands-on coaching, mentoring, and training.

Skills

Quality Assurance
Leadership
GMP Environment Experience
Auditing
Validation Activities

Job description

Job Description

QA Manager

I am partnered with an international advanced pharmaceutical and medical device business that is investing seriously into expanding their quality and operational activities, especially across various sites within the UK.

After the appointment of a new senior quality leadership team, the business is now looking to bring in new management across critical sites.

Working as a form of QA head for their own respective site, this position will manage a small team and remain fully hands-on in all areas of quality. This includes systems oversight, operational delivery, and validation activities.

A core aspect of the role will be leadership – leading a small team through hands-on coaching, mentoring, and training.

If you are looking for a varied position that offers you a chance to make a real impact on your own site and play a significant part in the way that quality assurance is adopted and implemented business-wide, please apply below or contact Mark Bux-Ryan for further information.

Key Experience:
  • Experienced within a QA capacity, working in a GMP environment
  • Ideally working experience of a sterile / aseptic environment – working within a terminally sterile setting would be helpful – these are not essential
  • Leadership and management experience
  • Strong hands-on experience of a range of quality activities, especially in relation to QMS oversight
  • Auditing experience essential – if you have been a lead auditor, this would be advantageous
  • Knowledge and experience of validation activities
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