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Qa Manager

RBW Consulting

Stoke-on-Trent

On-site

GBP 60,000 - 80,000

Yesterday
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Job summary

An established industry player is seeking a dynamic QA Manager to lead quality assurance efforts at their site. This pivotal role involves managing a small team while remaining hands-on in quality oversight, operational delivery, and validation activities. With a focus on coaching and mentoring, you will have the opportunity to make a significant impact on quality assurance practices across the business. If you thrive in a fast-paced environment and are passionate about quality management in the pharmaceutical sector, this is the perfect opportunity for you to excel and drive change.

Qualifications

  • Erfahrung im Qualitätsmanagement in einer GMP-Umgebung.
  • Führungserfahrung und starke praktische Kenntnisse in Qualitätsaktivitäten.

Responsibilities

  • Leitung eines kleinen QA-Teams und praktische Coaching-Erfahrungen.
  • Überwachung von Qualitätssystemen und operativer Lieferung.

Skills

Qualitätsmanagement (QA)

GMP-Umgebung

Führungskompetenz

Auditing

Validierungsaktivitäten

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:

  1. Experienced within a QA capacity, working in a GMP environment
  2. Ideally working experience of a sterile/aseptic environment working within a terminally sterile setting would be helpful, these are not essential
  3. Leadership and management experience is preferred
  4. Strong hands-on experience of a range of quality activities, especially in relation to QMS oversight
  5. Auditing experience essential; if you have been a lead auditor, this would be advantageous
  6. Knowledge and experience of validation activities
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