• Growing pharmaceutical organization
• Cross functional and regional collaboration
• Exciting career progression path
Responsibilities:
• Oversight of contract manufacturers and 3PLs in quality assurance
• Conduct due diligence checks, evaluate batch documentation and ensure overall systems, products and processes to meet quality and relevant regulatory requirements.
• Lead the development and implementation of quality initiatives to address product, process and system inadequacies to achieve continual quality improvement objectives
• Maintain QMS eg. Change control, deviations, CAPA, customer complaints etc.
• Conduct internal and external audits as required
Requirements:
· At least 1-2 years of quality assurance working experience in pharmaceutical industry
· Degree or diploma in pharmacy, or relevant discipline.
· Working knowledge of GMP and GDP in the pharmaceutical industry
· Motivated and driven personality
How to Apply:
• Interested applicants may apply by sending in your updated résumé (in MS Word format) to my email or apply directly:
• Consultant: Tan Wei Xiang
• EA personnel reg. no.- R1658660
• EA License No. 17C8502
