PV Quality Director
Global Pharma
Permanent
Hertfordshire - Flexible working
up to 69,000, plus bonus & car allowance
We are looking for a PV Quality Director to join a leading global pharmaceutical company, within their diverse and collaborative team. You will lead and oversee investigations, planning and implementation around process deficiencies and non-compliances.
Key Responsibilities
-Determining if a finding/deviation is valid and assigning criticality to leading Root Cause Analysis activities
-CAPA: Drafting corrective action and preventive action plans and effectiveness measures and overseeing CAPA plan implementation
-Identifying and escalating issues if timelines may be at risk
-Performing trend analysis on data alongside subject matter experts and Global Process Owner (GPO)
-Supporting the conduct of GVP audits and inspections
-Leading other PV system related QMS activities, as required
Key Requirements
-
-Bachelors Degree (in life sciences or a healthcare related discipline)
-Strong, demonstrated experience in pharmacovigilance, especially post market
-Able to build strong stakeholder relationships
-Ability to work independently on complex and/or multiple projects
-Detailed knowledge of key GVP regulatory requirements, in particular those relating to quality and quality management systems.
- Agency: Cpl Life Sciences
- Reference: JO-2204-490560
Website: Cpl Life Sciences
- Posted: 3rd May 2022
- Expires: 31st May 2022
