Job Scope:
1. Maintain site-wide compliance by ensuring all activities and documentation are current, effective, and in-use.
2. Ensure all Internal and External Audit including Third Party Audit Preparations are complete.
3. Assist in supplier accreditation/qualification and ensure compliance to required documentation.
4. Support in ensuring management of all Quality Management System-related documents.
Duties & Responsibilities:
Responsible for monitoring and maintaining completeness of documentation in all GMP processes in the company.
Ensure all documentation for supplier accreditation/qualification are complete and current in compliance with regulations and customer requirements.
Ensure annual training requirement for the company is complied with.
Support safekeeping of all documents registered under Document Control Center.
Facilitate Internal Quality Audit Team and its functional activities.
Facilitate all external audits (Regulatory and Certifying bodies, Clients/Customers).
Support in executing continuous improvement actions and projects.
Ensure compliance with cGMP/GDP, FDA, Halal, FSSC, customer, and other regulatory and statutory requirements.
Provide assistance in deviation investigation, robust CAPA identification, and implementation.
Perform other related tasks assigned by immediate supervisor/management.
Education:
Preferably a graduate of Food Technologist, Chemistry, Pharmacy, or related Course with 2-3 years working experience of equivalent specialization.
Years of Related Work Experience:
With at least 3 years working experience applying expertise in document review, audit, regulations, standards, supplier accreditation, document and change management, and deviation handling in any of the Business Industries in Veterinary Food, Cosmetics, and Pharmaceutical.
Job Type: Full-time
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