Quality Assurance Manager
i-Pharm Consulting
Wellington, New Zealand
21h ago
source : Jobg8 Ltd.

This position offers a unique blend of GMP and pharmaceutical research to someone looking for their next opportunity.

If you have a strong GMP pharmaceutical background, and are confident leading a small team, this could be your next career move.

This will be a hands on role seeking an individual who will not only react to the demands of a project, but proactively make improvements to the full QMS.


  • Responsible for the release of any GMP products to clients
  • Principle contact for all Medsafe correspondence and audits
  • Key contact for all CRO clients
  • Responsible for the continuous improvment of the QMS
  • Managing a small team of 3
  • Maintain and adhering to Medsafe regulations
  • QMS Matrix training

  • Life sciences degree (pharmacy preferred)
  • Experience on managing QMS Medsafe compliance
  • People management is a pre-requisite
  • Pharmaceutical experience is a must
  • CRO experience will be a strong advantage

    i-Pharm Consulting is a specialist Recruitment Company servicing the global Pharmaceutical industry. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs).

    i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.


    If you would like to discuss this vacancy further, please call Recruitment Consultant, Rachel Jennings on (0) 2 (tel : 2 ), or email (mailto : ).

    If this role is not suitable, Rachel is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


    Senior Quality Assurance Associate, Quality Manager, Senior QA Associate, Senior Quality Systems Associate, Quality Assurance Manager, Quality, MAA, CTA, CRO, Labelling, Regulatory Operations, Regulatory Associate, Senior Regulatory Associate, Submissions / Documentation, QMS, CAPA, Pharmaceutical

    Report this job

    Thank you for reporting this job!

    Your feedback will help us improve the quality of our services.

    My Email
    By clicking on "Continue", I give neuvoo consent to process my data and to send me email alerts, as detailed in neuvoo's Privacy Policy . I may withdraw my consent or unsubscribe at any time.
    Application form