puestos de Pharmaceutical en Malasia

Our client specializes in the research, development, production, and sales of daily chemical raw materials, including cosmetic active ingredients, raw materials, and synthetic perfumes. They operate two major production bases in Suqian City, Jiangsu Province, and Ma'anshan City, Anhui Province. The Ma'anshan City production base, through its subsidiary, was constructed according to GMP guidelines for APIs and has passed the FDA on-site audit.

Job Description:

• Review and approve quality-related documents, and conduct product quality reviews.
• Release or reject APIs and intermediates, including raw materials, packaging, and labeling materials.
• Ensure investigation and resolution of critical deviations and quality complaints.
• Approve all specifications, master production instructions, and procedures impacting product quality, including those for contract manufacturers.
• Oversee internal audits, and ensure maintenance and calibration of critical equipment.
• Ensure proper material testing and reporting, including stability data to support retest/expiry dates and storage conditions.

Job Requirement:

• Bachelor's degree or higher in Chemistry, Biology, Pharmacy, or related field.
• Minimum 7 years in the pharmaceutical industry, with at least 5 years in a QA Manager role.
• In-depth knowledge of ICH Q7 guidelines, FDA, and EDQM audit processes.
• Proven experience leading quality organizations in a global matrix environment. Ability to make quality decisions in challenging situations.
• Proficiency in written and verbal English. Mandarin is a plus.
• Strong leadership, interpersonal, and communication skills.