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QA Supervisor

Job description

Our client a major manufacturer in Clare has a vacancy for a QA Supervisor

The role is structured so that he/she will have :

Responsibility for the production of certificates to include:

  • Speed
  • Authenticity and quality
  • Ease of access / availability.
  • Layout and embellishing
  • Upgrading

Ideally the candidiate should possess, 2-3 years experience within a GMP manufacturing facility.

The successful candidate will have the following:

  • 3 Years experience in QA within a regulated environment ie. Pharma, Med Devices etc..
  • Providing QA and oversight of cGMP activities across the site.
  • Ensure operations and support departments are in compliance with cGMP.
  • Internal auditing. Carry out preparation, scheduling, reporting & follow up of internal audits.
  • In conjunction with the internal audit team.prepare, schedule, carry out, generate audit reports.
  • Ensure Qualified Person support for site and global batch release.
  • Documentation – working closely with the QA Officers responsible for control of documentation.
  • Responsibility for production of documentation, communication & training to appropriate stakeholders
  • Updating of the intranet and review on an ongoing basis. Intranet, update, review, training records 
  • Ensure preparation and support for internal & external audits.
  • Work collaboratively with support departments while ensuring high cGMP standards.
  • Ensure effective stakeholder management for corporate support departments. 
  • Strong leadership and personnel development skills.

An excellent salary package is on offer. 

Diploma/Degree in Science required with IS0 9001:2000 & 17025  an advantage.

For more information please mail codonnell@sigmar.ie

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