about 1 year ago
A fast-growing rare disease pharma is looking for a QA Director to join their team on a permanent basis. The company is at an exciting stage and major phase of growth with a multiple of products in the process of being launched out to the market.
Key responsibilities but not limited to:
• Responsible for ensuring that the site is GMP compliant.
• To ensure that the key elements of the Quality Management System relating to cGMP are effect effectively implemented to ensure that the company is operating in compliance with GMP guidelines.
• To be acting QP and responsible for batch releases.
• Responsible for hosting EMA & FDA inspections and to make sure that the site is always inspection ready.
If you are an experienced QP looking for a new challenge, please don’t hesitate to get in touch!