The Quality Control Analyst should be a Chemist. Preferably has experience in pharmaceutical manufacturing company and working knowledge of Good Laboratory Practices (GLP), Laboratory Safety, Good Manufacturing Practices (GMP), and PIC/S (Pharmaceutical Inspection Co- Operation Scheme).
Duties and Responsibilities:
- Performs sampling and conducts physical and chemical analysis of raw materials, in process products, finished goods and packaging materials in accordance with approved procedures and established test methods.
- Prepares Standard Operating Procedures (SOPs) and Work Instruction (WI's) applicable to the operation of QC Laboratory.
- Assists in the investigation of the root cause of deviation (Out- of - Specification) and in formulating corrective and preventive actions.
- Conducts and monitors the working condition and calibration of laboratory instruments. Ensures that instruments/ equipment is maintained in good repair and under calibrated status. Maintains equipment maintenance and calibration records.
- Conducts in-process inspection of manufacturing operations. Communicates to QC Manager and Production Management any deviations noted for outright correction.
- Provides data for Annual Product Quality Reviews, Validation and Risk Assessment in the areas of responsibility.
- Collaborates with the Production in conducting process validation and equipment cleaning and sanitation validation.
-Trains other analyst to perform laboratory procedures and assays, performs other related tasks given by superiors.
- Ensures that laboratory facilities, systems and procedures conform to PIC/S- GMP, 5S standards and safety requirements.
Job Type: Full-time
Pay: Php18,
- 00 - Php20,000.00 per month
Schedule: - 10 hour shift
8 hour shiftSupplemental pay types:
13th month salary
