Description
Role Purpose:- Function as one of the Qualified Persons on-site ensuring that practices and products released from the site Genzyme (Ireland) Ltd are in compliance with cGMP as stated in Directive /EC and in the Rules and Guidance for Pharmaceutical manufacturers and Distributors 2007.
- Provide oversight and support improvement of site quality systems and GMP practices.
- Review and approval of quality documentation.
- Lead quality improvement projects.
- Work with relevant departments to ensure timely closure of quality actions.
- Ensure continued site wide compliance to cGMP.
- Provide support and direction for all departments in quality related issues.
Qualifications:
- Third level qualification (Degree in science or related discipline)
- Qualified Person status
Experience:
- Previous experience working in a similar role a distinct advantage
- Minimum of five years' experience in Quality role
- Very good knowledge of cGMP in a regulated environment
- Excellent interpersonal skills and communication skills
- Leadership experience is an advantage
- Focused on achieving results
- Risk Management
- Validation
- Flexible approach and influential
If you are interested in this position please contact me on or reply to this advert with your most recent CV. We also offer €200 worth of shopping vouchers for any successful referrals.