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QA Manager

RBW Consulting LLP

Stoke upon Tern

On-site

GBP 60,000 - 80,000

2 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 efforts at their site. This is a hands-on role that involves managing a small team and ensuring compliance with quality standards. The position offers a unique opportunity to make a significant impact on quality assurance practices across the business. Ideal candidates will have experience in a GMP environment, strong leadership skills, and a background in auditing and validation activities. Join a forward-thinking organization dedicated to quality and operational excellence.

Qualifications

  • Experience in QA roles within GMP environments is essential.
  • Leadership and management experience preferred for team oversight.

Responsibilities

  • Lead and manage a small team in quality assurance activities.
  • Oversee systems, operational delivery, and validation processes.

Skills

QA Management

GMP Environment Experience

Leadership

Auditing

Validation Activities

QMS Oversight

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 is preferred
  • 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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