← Back to opportunities
About the Role
About the Role
We are looking for an experienced Deviation Management Engineer to support our client, a leading global pharmaceutical company, in managing a surge in site deviations. The successful candidate will be embedded within the Quality team and play a critical role in ensuring all deviations are investigated and closed within the required 30-day regulatory timeline.
Key Responsibilities
- Lead end-to-end deviation investigations, including root cause analysis and impact assessment
- Manage and prioritise a backlog of open deviations to meet closure deadlines
- Liaise with cross-functional stakeholders across Manufacturing, QA, QC, and Engineering to drive timely investigation and sign-off
- Develop, assign, and implement Corrective and Preventive Actions (CAPAs) arising from investigations
- Author high-quality deviation reports and investigation summaries in line with GMP documentation sta...
Ready to Join Through a Referral?
Apply now and get connected directly with the hiring team
Apply for this Position