About the Role:
Global Auditor of Product Quality (GMP)
An internationally established Pharmaceutical company are looking for a Quality Auditor as part of their Global auditing team, strategically linking up with counterparts around the world ensuring Quality is kept to the high standards the company demand.
They're looking for an independent and motivated Auditor. This is a new role with high visibility, and you'll be given ownership of the Quality Auditing across their European remit. With a background in Pharmaceuticals and Auditing, you'll be able to hit the ground running, working flexibly yet decisively at a strategic level.
What will you be doing?
As Auditor of Global Product Quality, you will be responsible for supporting auditing and monitoring of outsourced GMP contracted activities and GMP suppliers. You will work with other functional departments to establish and maintain the effectiveness of quality systems to support good manufacturing practice audit programs. In addition to this, you will lead and conduct audits of contractors and suppliers to ensure compliance with applicable regulatory requirements. The position would be based in their office near Slough, and would require up to 50% travel; mostly European with occasional long-haul travel.
What skills should you have?
- A wealth of experience in pharmaceutical manufacturing and/or manufacturing device, QA or QC role
- Working knowledge of GMP (global manufacturing practice), GDP (global distribution practice) and QSR (quality systems regulations)
- Experience using Trackwise, MS Word and Excel
If you would like to express interest, please get in touch detailing your experience within the areas above and call in for Dan Abbott to discuss the application process