Position Purpose:
Responsible for managing and supporting site investigations related to deviations, OOS (Out of Specification), OOT (Out of Trend), microbial excursions, and manufacturing non-conformances within a GMP-regulated environment.
Key Responsibility:
- Lead and support investigations for deviations, OOS, OOT, and market complaints using structured root cause analysis methodologies.
- Conduct microbial investigations, impact assessments, and CAPA implementation to ensure regulatory compliance and prevent recurrence.
- Collaborate with cross-functional teams to drive timely closure of quality events and achieve effective investigation outcomes.
- Review investigation reports, assess data integrity, and ensure compliance with GMP, GDP, and ALCOA principles.
- Perform trend analysis of quality events and provide recommendations for continuous improvement.
- Support internal and external audits, including audit responses and compliance readiness activities.
- Manage investigation tracking, documentation control, and QMS activities through TrackWise and other quality systems.
- Coordinate department training programs, SAP SuccessFactors learning management activities, and employee qualification compliance.
- Act as a reviewer and technical resource for investigation strategies, risk assessments, and quality decision-making processes.
Education Qualifications:
- Minimum Bachelor's Degree in Biotechnology, Chemical Engineering, or any Engineering-related field.