QC Pharma Projects Supervisor
Core
Lead a team of 8-12 staff to oversee QC Pharma Projects supporting operations cleaning validations, residual monitoring, and method transfers to the QC laboratory.
Role type
Senior IC QC Projects Supervisor
Builds
GMP-compliant analytical support for cleaning validations, residual monitoring, and method transfers
Domain
Pharmaceutical manufacturing / Quality Control
Required skills
GMP/GLP compliance, team leadership, analytical scheduling, HPLC/GC operation, Empower software, regulatory inspection readiness, new product introduction support
Preferred skills
Chemistry background, problem-solving, conflict handling, succession planning
Technologies
HPLC, GC, Empower
Responsibilities
Provide guidance to ensure GMP-compliant activities; manage team performance and training; represent company during regulatory inspections; schedule analytical support for validations and monitoring; lead New Product Introductions analytically
Seniority
Senior, hands-on IC
