长沙招聘

任职要求：
1. University Degree or above, major in food, nutrition, chemistry, pharmacy or pharmacology.
2. Have product registration experience in health Food or Pharmaceutical Company at least 6 years. And within which at least 2 years with supervisor or management experience.
3. Be familiar with health food regulation or knew the regulation about medicine and pharmaceutical.
4. Be familiar with GMP for health food or pharmaceutical for powder, liquid and solid products.
5. Read and write English fluently.
6. Must be proficient in Microsoft Office Programs eg. Word, Excel, PowerPoint and Outlook
7. Good Communication Skill and teamwork.
8. Work Location: Preferred Suzhou, Optional Shanghai

职位职责：
1. Responsible for all the China factory regulatory activities.
2. Proactively develop and implement continuous improvement program for the regulatory department to assist Quality & Regulatory department to create a world class manufacturing operation.
3. Develop and maintain good working relationships with various government authorities related to quality, hygiene, health, labeling and standards.
4. Responsible for transfer application, local product registration, standards registration and associated testing. Keep track of all expiration date of related quality related license and obtain renewal within 10 days from expiration.
5.Manage product development activities in relation to regulatory, registration and getting of all necessary documentation including raw material specifications, in-process and finished product specification.
6. Develop and maintain calendar of regulatory and licensing dates / deadlines and needs to ensure product licensing and registration is always completes in a timely manner with zero risk to supply chains.
7. Get some information for the new China regulatory on time and update the relevant standard operation procedures. Support the license projects such as GMP and TGA certificate.
8. Contract and keep good relationship with the raw materials vendors for getting necessary registration documents.
9. Find a suitable clinical testing authority laboratory with lower price in the China. Follow up the stability, safety, function and clinical testing with province CDC or suitable laboratory within 10 days from deadline.
10. Renew all of current health food certificates according to Chine regulatory within six months after the SFDA publish the new regulatory.
11. Do Agile approval for all of labels changes for China Marketing. Also be in charge of formula approval for new products in the Agile system.

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