Process Engineer
Core
Conducting incident investigations and defining corrective and preventive actions in a pharmaceutical manufacturing environment.
Role type
Process Engineer (Pharmaceutical Manufacturing)
Builds
Ensures compliance and operational stability in sterile product manufacturing
Domain
Pharmaceutical Industry / GMP
Deliverable
dashboards & analysis
Required skills
GMP documentation, incident investigation, root cause analysis, corrective and preventive action (CAPA) planning, CAPA verification, incident reporting, follow-up task management
Preferred skills
sterile product handling, GQTS, pDOCS, SAP, Veeva Vault (eQMS)
Responsibilities
Conduct incident investigations, document cause of incidents, define and document CAPAs, verify effectiveness of CAPAs, monitor and report on investigations, initiate follow-up tasks
Seniority
Mid-level (2+ years experience)