衡阳招聘

Job Description:

1. Be In charge of site drug production and technical management and related work.

2. Prepare the production related documents such as BMR and validation related documents.

3. Take the responsibility of site inspection of quality hygiene and process, review the BMR and ensure the implementation of all related SOPs, ensure the compliance of GMP.

4. Coordinate with FR & D and other related technical dept to facilitate the new product technical transfer and trouble shooting related work.

5.Take on other duties as assigned by superior.

Working Ability:

1. Be active with work.

2. Be good at manufacturing site management in GMP facility.

3. With the ability of identifying and solve the problem during drug manufacturing;

4. Have the ability of technical management

5. Have the concerned working experience of pharmaceutical production, quality management and GMP inspection.

6. Be familiar with GMP and validation will be preferable.

昆山龙灯瑞迪制药有限公司是由加拿大龙灯集团与印度瑞迪博士制药有限公司及昆山双鹤制药有限公司三方合资的一高新技术制药企业，公司主要生产经营医药原料及制剂产品。“引导健康新生活”是公司的核心目标，我们立志为人类健康事业做出应有的贡献。公司诚邀各界有识之士加盟“龙灯瑞迪”，共同创造美好未来。