QC Stability & Analytical Development Supervisor
About this position
The QC Stability & Analytical Development Supervisor is responsible for managing and supervising all activities related to product stability testing and analytical methods.
Responsibilities
• Responsible for managing and supervising all activities related to product stability testing and analytical method.
• Review monthly reports related to protocol of stability testing and analytical method report.
• Review SOP/Form/List related to test and its related stability testing report and analytical method.
• Review related to Worksheet for stability testing report and analytical method.
• Review monthly reports regarding temperature of stability room, review verification data of measuring instruments (analytical balance, ph meter, meter conductivity, termohygrometer, etc) and evaluation report if any deviation founded.
• Prepare SOP related to test and its related supporting activities in laboratorium.
• Make a PJE (Application for Engineering Services) if there is damage or modification that can be done by an internal technician.
• Provide training and qualify subordinates.
Requirements
• Pharmacist with at least 2 years experiences.
• Responsible, hard worker, fast learner, and strong leadership.
• Able to work individually and with team as well.
• Have received training and understand the Good Manufacturing Practices (CPOB).
• Fluent in English both speaking and writing.