Quality Manager

WHAT DOES THE ROLE ENTAIL?

As a Quality Manager, you'll Support business growth by advising and participating in the implementation of projects from a quality and regulatory point of view. Also, you will -

• Compliance across the business with all HPRA/Department of Health requirements and aim to eliminate non-compliance findings during regulatory inspections.
• Maintain professional knowledge of relevant and current regulatory requirements within the EU and Ireland .
• Supporting the validation and qualification agenda for QA for all Computer systems and critical equipment for Life Sciences sites.
• CAPA Management: tracking, trending and reporting
• Support the Quality Management team with Regulatory Agency/ Certified body audits.
• Act as Deputy RP on the WDA and carry out responsibilities delegated by the RP.

WHAT DO WE NEED FROM YOU?

• Minimum 5 years experience in QA/QC within the Pharmaceutical/Medical Devices Industry.
• Proven track record in QA (inc. Auditing) in a GMP/GDP/GCP/GxP environment.
• Experience with hosting regulatory and client audits.
• Management of Quality Systems in compliance with GxP
• Excellent people management skills

WHY CHOOSE US?

As well as competitive pay rates, you will be entitled to an award-winning range of benefits including:

• Free confidential 24/7 GP service
• Hundreds of discounts (including retail, childcare + gym)
• Affordable loans & enhanced pension scheme
• 24/7 employee support service for you (+ family) with access to free counselling and much more: https://careers.dhl.com/global/en/dsc-benefits

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