• 5-7 years of experience in preparation and execution of validation protocols [Manufacturing
and supporting processes]. Understanding and knowledge of cGMP, GLP, SOP issue and periodic updates
• Experience in cGMP/GDP/GLP Audit management and liaison with regulatory authorities is highly preferred along with Internal Quality Audit skills. Perform investigations and execute the CAPAs
The selected candidates must possess a degree
in Science / Pharmacy and experienced in
The career path, salary and other benefits shall be
in par with the best in the pharmaceutical sector.
Please send in your CV, within 10 days, to [Click Here to Email Your Resume] in strict confidence.
ICM Pharma Pte. Ltd