French company, mainly produces raw materials of paracetamol powder, granules and other pharmaceutical intermediates.

Objectives:
1. To supervise all quality related activities and to ensure the plant operation is in line with the GMP requirements and the registration files.
2. To be involved in and provided guidance for all quality matters of the site.
3. To review and approve all appropriate quality related documents.

Main missions:
1. To ensure all quality assurance procedures and methods are correctly implemented based on GMP requirements.
2. To ensure all manufacturing activities (including all activities going from purchasing of raw materials, production, control, storage and shipment) are carried out in line with the relevant GMP requirements, and in accordance with the registration files.
3. To manage the staff of the quality department to ensure the efficiency and effectiveness and the smooth cooperation with other departments.
4. HSE and 5S in the area comply with Seqens requirements
5. Other tasks assigned by the superior.

Job Requirements:
1. Bachelor degree of Sciences, Chemistry or other equivalent major (e.g. Microbiology, Pharmacy, Pharmaceutical Sciences, Chemical Engineer, etc.); With knowledge of analytical chemistry.
2. No less than 10 years of work experiences, at least 5-year of senior quality management experience or having worked in a GMP or QA/QC environment, in a pharmaceutical or an active pharmaceutical ingredients plant.
3. Experienced with proven track records in communicating with regulatory officials, hosting regulatory inspections (e.g. EU, NMPA, FDA, Health Canada, etc.), and