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QA Manager

RBW Consulting

South Yorkshire

On-site

GBP 40,000 - 80,000

Full time

25 days ago

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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 role offers the opportunity to manage a small team while being hands-on in various quality activities, including systems oversight and validation. With a focus on leadership, you will coach and mentor your team, ensuring the adoption of quality practices across the organization. If you are passionate about making a significant impact in a GMP environment and thrive in a role that combines management with operational tasks, this position is perfect for you.

Qualifications

  • Erfahrung in der QA in einer GMP-Umgebung ist erforderlich.
  • Führungserfahrung und Kenntnisse in Validierungsaktivitäten sind von Vorteil.

Responsibilities

  • Leitung eines kleinen QA-Teams und aktive Beteiligung an Qualitätsaktivitäten.
  • Überwachung von Systemen und operativer Lieferung in der Qualitätssicherung.

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:
  • 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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