Senior Specialist Process Excellence
Core
Manage quality events (CAPAs, deviations, complaints) and support inspection readiness and regulatory audits for pharmaceutical manufacturing.
Role type
Senior Specialist Process Excellence Compliance
Builds
GMP-compliant manufacturing processes and documentation
Domain
Life Sciences / Pharmaceutical Manufacturing
Required skills
GMP compliance, root cause analysis, risk evaluation, regulatory audit preparation, continuous improvement, project management
Preferred skills
Knowledge of Oral Solid Dosage (OSD) systems, impact assessments
Technologies
Electronic document management systems
Responsibilities
Own quality events and associated actions, Author and maintain GMP documentation, Contribute to inspection readiness and regulatory audits, Support root cause analysis, Contribute to quality KPI adherence, Perform impact assessments and risk evaluations, Drive local continuous improvement and site initiatives
Seniority
Senior, hands-on IC