Description
Qualified Person - London - 12 Month Contract
Main Responsibilities:
- Primarily responsible for batch release of company products.
- Accountable for the implementation, sustainability and benefit delivery of site changes/initiatives within own team.
- Provide support for resolution of technical problems
- Promote QMS and actively encourage input/development of QMS
- Provide direction and oversight for the functional environmental, health and safety (EHS) programs. Review and approve facility, equipment and process risk assessments; drive appropriate system and operational changes; and provide leadership for improvements in process.
- Work with the Business Unit to implement an effective audit programme and ensure audit readiness at all times
- Lead and support level 2/3/4 audits
Key Requirements:
QP status
Experience of effectively leading and managing technical, professional teams
Ability to deliver communication with clarity, impact and tailored to audience.
Knowledge and application of the principle of Quality Management System (QMS)
Detailed knowledge of current Good Manufacturing Practice requirements within major pharmaceutical markets
If interested please respond with an updated C.V.