- The Deviation Management Specialist provides day-to-day technical and scientific support to manufacturing operations within Merck’s Manufacturing Division (MMD)
- This role focuses on the investigation, resolution, and reduction of process deviations in a cGMP environment, supporting aseptic manufacturing, testing, planning, and release activities
- The Specialist works cross-functionally to lead manufacturing and laboratory investigations, implement corrective and preventive actions (CAPAs), and apply sound scientific and engineering principles to ensure product quality and compliance
- Provide daily technical support to manufacturing operations, including deviation identification, investigation, and resolution
- Lead manufacturing and laboratory investigations for atypical events using structured root cause analysis methodologies
- Develop, implement, and track corrective and preventive actions (CAPAs) to reduce recurrence of deviations
- Troubleshoot laboratory test failures and manufacturing process anomalies
- Apply critical analytical thinking to analyze complex problems and design/execute laboratory or pilot-scale experiments as needed
- Partner with cross-functional teams supporting aseptic manufacturing, testing, planning, and product release
- Develop and maintain strong working relationships with internal stakeholders across manufacturing and technical groups
- Document investigations and outcomes clearly and compliantly in accordance with cGMP requirements
- Provide shop floor support, including clean room gowning, to support deviation investigations
Support off-shift activities as required to meet operational and investigation timelines