Quality and Regulatory Affairs Manager

Wicklow  ‐ Onsite
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Description

Quality and Regulatory Affairs Manager

Pharmaceutical company is seeking a Quality and Regulatory Affairs Manager for their API site in Co. Wicklow.

Day to Day:
  • Responsible for managing the Quality function at the company.
  • Coordinate QC test and release activities, finished product, and intermediates to ensure product release to plan.
  • Manage analytical method transfer projects from S-A sites or from customers.
  • Prepare analytical validation protocols, review and approve reports.
  • Coordinate contract laboratories for QC, Micro.& Environmental testing.
  • Manage in-house and customer stability requirements for all API`s.
  • Primary point of contact for Regulatory bodies and customer related quality issues.
  • Manage and guide the activities of QA/QC staff to ensure compliance with regulatory requirements.
  • Deliver regular training to all staff via the Quality function.
  • Overall responsibility for maintaining and developing the site Validation Master Plan and Quality systems. Schedule, manage customer audits; ensure timely response and close out.
  • Manage dept. budget while actively pursuing cost reduction opportunities
  • Perform internal, external audits (Supplier, Quality, Environmental, Corporate) as required.
  • Prepare, approve Technical and Quality agreements.

Requirements:
  • Degree (Chemistry, Chemical Engineering, Pharmacy, Biological Science).
  • Significant experience of senior quality role in cGMP regulated environment

An attractive salary and benefits package is on offer please contact me Anna Mooney for more information on the company and the role.
Start date
06/2015
From
Real Staffing
Published at
16.07.2015
Project ID:
945822
Contract type
Permanent
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