The position requires a graduate of Chemical Engineering, a Bachelor in Pharmacy/Chemistry/Biology, or any related course. At least three years of extensive experience in chemical and microbiological analysis and a broad knowledge of GLP is necessary.
Job Summary:
The Senior Quality Control Analyst is in-charge of the scheduling and testing of product and materials in the QC Laboratory, as well as the preparation of Quality Reports.
Duties and Responsibilities:
- Conducts required tests and studies on products and operating environment.
- Participates in investigation of Lab Issues and Out of Specification test results.
Prepares Quality reports, including analytical reports (for raw materials and finished products) and Certificates of Analytical, for finished products and validation reports.- Creates and executes method development and method validation test protocols for finished products and generates the appropriate analytical methods.
Prepares analytical procedures using current pharmacopoeias.
- Participates in the review and update of existing analytical methods.
Maintains accurate and comprehensive lab analysis records, reference standards history, and reference organism history.- Coordinates with Production regarding Batch testing and with IPC regarding RM testing.
Provides mentoring and training to Junior Analysts, Technicians, Aides regarding methods and GLP.
- Responsible for good cooperation among the laboratory personnel.
Responsible for the cleanliness and discipline in the working area.- Willing to assigned in San Mateo Rizal.
Job Types: Full-time, Permanent
Pay: Php20,- 00 - Php21,000.00 per month
Benefits: - Company events
Free parking
Opportunities for promotion- Promotion to permanent employee
Schedule:Supplemental Pay: Overtime pay
