KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Quality Specialist will be varied however the key duties and responsibilities are as follows:
Carry out Compliance and Operational Quality Assurance tasks, for example; maintenance of the QMS and production of batch record reviews.
Lead internal audits and support external inspections.
Provide guidance and coaching to other departments across the business to ensure GMP and best practice compliance.
Monitor Quality KPI's, generate and review Quality Assurance procedures; training and coaching junior members of the team.
To be successful in your application to this exciting opportunity as the Quality Specialist we are looking to identify the following on your profile and past history:
Some experience of leading or supervising Quality Teams
Proven industry experience within a GMP Pharmaceutical business
3. A working knowledge and practical experience of maintaining a QMS
Key Words: QMS, QA, Quality Assurance, GMP, Pharmaceutical, Drug Development, Quality Management System.