Company Background:
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 Maanshan City Anhui Province. The Maanshan City production base through its subsidiary SINOBEST Cosmeceutical Co. Ltd. was constructed according to GMP guidelines for APIs and has passed the FDA onsite audit.
Job Description:
- Review and approve qualityrelated 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:
- Bachelors 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.
- Indepth 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.
Salary Range:
Open for discussion