Senior Quality Manager & QP (Contract) - South East
Pharmaceutical Company embarking on a period of growth as a multi-site GMP Manufacturing.
Snapshot summary of role (Below)
If you are an Interim Senior Pharmaceutical Quality professional & QP with availability for full timer obligations - please get in touch
Responsibilities: To act as Senior Quality Manager & QP - with job responsibilities that include but are not limited to:
- Develoment of Quality Strategy for highest level of Compliance
- Support on-going regulatory surveillance and industry benchmarking
- Act as the responsible person in line with applicable directives & regulations for the communications with Health Authorities, Recalls and Defect reporting
- Work with functional GxP Quality teams to assist in the strategic preparation for and management of global regulatory inspections as required and using principles of Quality Risk Management. Assist in the review of written responses to regulatory inspectional observations and/or health authority reports, as requested.
Requirements
- Experience leading or supporting commercial manufacturing sites through global health authority inspections
- Ability to identify and implement phase-appropriate compliance strategies
- Qualified QP
I look forward to hearing from you
Simon Fowler - Contract Pharmaceutical Recruitment Specialist - Science Solutions