Job Summary:To ensure all products, in-process materials, production facilities, and processes are in compliance with the Company's Quality Management standards and the Government's cGMP requirements through proper monitoring procedures, an effective training program, and up-to-date documentation. Conduct and support the Company's research and development projects.Job Roles and Responsibilities:? Develop and maintain Standard Operating Procedures (SOPs).? Provide effective training to production staff.? Monitor performance of products, operations, and equipment against standards, promptly attend to changes and deviations.? Review and make recommendations for improvement in areas of safety, environment, sanitation, and hygiene.? Assist and ensure all validations are conducted timely and accordingly.? Assist and review production batch records that have all the necessary information for final approval and release decision.? Conduct and support the Company's research and development projects.? Any other production-related duties that may be assigned by management as occasions arise.Requirements:? Degree holder or above in Pharmacy? Registered / Licensed Pharmacist with a valid practicing certificate in the Philippines.? One year of supervisory experience in Pharmaceutical manufacturing in a GMP environment is an advantage.? Less experienced applicants are welcome as comprehensive training will be provided.? Excellent command of spoken and written EnglishJob Types: Full-time, PermanentSalary: Php20,000.00 - Php25,000.00 per monthBenefits:
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