Lab / QC Supervisor (Pharmaceutical)

About the Company: Our client is one of the leading pharmaceutical ophthalmic solutions manufacturers in the world, dedicated to providing sterile pharmaceutical ophthalmologic solutions, from prevention to delivery of care at every touchpoint, advancing wellness in hospitals, clinics, and home-care sectors. Position Overview: The incumbent works closely with the QC Manager on all aspects of Quality Control in the laboratory, in particular, on product reliability and compliance with all established product standards. Ensures that all aspects of quality within the organization are upheld. Responsibilities: Able to provide guidance and coach lab technicians. The incumbent inspects all incoming raw material for compliance according to current standards. The incumbent conducts periodic checks and analysis on all WIPs. The incumbent retains finished product samples from production to conduct checks and analysis. Assist QA on failure analyses, corrective and preventive action response to customer complaints. Assist in GMP audits, validation, qualification, and change control. Assist in maintaining Product Quality and Technical File. Write technical papers or reports or prepare standards and specifications for processes, products, or tests. Requirements: Diploma/Degree in related field (Chemical Process Technology, Pharmaceutical, Chemistry, Biotechnology). Proven experience in the evaluation and validation of materials, products, or processes, adhering to regulatory standards. In-depth knowledge of the cGMP and ISO 13485. How to Apply: Interested candidates, please submit your updated resume by using the Apply button. *We regret to inform that only shortlisted candidates will be informed.* Contact: Sarah Sevilla Registration Number: R22107553 EA License No: 18C9027#J-18808-Ljbffr