Quality Control Analyst

Sampling and testing of raw materials, intermediates and finished products- Preparing Quality reports, including analytical reports (for raw materials and finished products)- Calibrating analytical equipment, as and when required.- Creating and executing method development and method validation test protocols for finished products and generating the appropriate analytical methods.- Perform routine and non-routine chemical analysis of products using standard operating procedures.- Write and execute chemical testing procedures.- Maintain up-to-date documents for chemical testing methods and activities.- Operate laboratory equipment safely and effectively to conduct testing.- Record, analyze and report test results to Managers.- Maintain inventory of chemicals and supplies in laboratory.- Supporting all QC activities.- Ensuring good relations and communications with all members of the team and responding politely and in a timely fashion to internal and external customers.- Perform various techniques like HPLC.- Observing and complying with Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP).**Minimum Qualifications**:- BS degree in a scientific or technical field preferably in Chemistry, life sciences and allied courses.- Must be a LICENSED CHEMICAL TECHNICIAN- Must have minimum of two years of direct lab experience in FDA-regulated pharmaceutical.- At least three (3) years experience in Quality Control in a pharmaceutical firm.Schedule:- 8 hour shiftAbility to commute/relocate:- Carmona, Cavite: Reliably commute or planning to relocate before starting work (required)