招聘：制剂研发总监（上海）

young

目前我集团上海研发中心在招聘一名制剂研发总监，向公司总经理汇报。

如有意向者，可投递简历至：yangl@hansoh.cn

 

职位介绍：

职位名称：制剂研发总监

工作地点：上海

Responsibilities:

· Developing formulation strategies for selected generic products, taking into account technical, regulatory and intellectual property considerations.

· Ensuring timely completion of new product development projects, specifically developing formulations bioequivalent to the reference products; developing manufacturing processes for the ANDA registration batches; directing/managing all activities associated with the registration batch manufacturing; authoring, reviewing and approving technical documents (protocols, batch records, specifications, development reports, etc.).

· Interacting with Manufacturing, Validation, and Materials Management to assure smooth scale up of formulations to commercial scale.

· Advising Manufacturing and Quality Operations of possible impact that deviations from prescribed operating conditions or procedures may have on products.

· Developing, interpreting and explaining standard practice instructions and procedures, and ensuring that they are complied with.

· Managing, training, and developing scientific staff. Maintaining effective communication within areas of responsibility.

· Responsibility and authority for matters such as maintaining quality, accuracy and quantity of work; giving advice, guidance, and direction; dealing with routine problems; developing detailed internal work methods; initiating recommendations on personnel matters.

· Monitor and appraise the performance of personnel reporting to the position

· Overseeing and/or collaborating with external parties involved with formulation development and/or manufacturing.

QUALIFICATIONS：

· A Science degree is required, preferably in Pharmaceutics or Chemistry. An advanced degree (PharmD, Masters, or PhD in a science related discipline) is strongly preferred.

· Minimum of 8-10 years of experience with pharmaceutical development programs, preferably with generic product development.

· Hands on experiences in developing and manufacturing solid oral dose product, especially modified release products.

· Solid understanding of cGMP.

· Excellent interpersonal, supervisory, investigative, and implementation skills.

· Must have desire to work and excel in a rapidly changing, small company environment where a “hands-on” approach is required.

· Must have strong leadership abilities.

· Requires the ability to influence others and communicate effectively, written and orally, both internally and externally.

· Must possess excellent written and verbal communication skills. Requires

the ability to prepare and review technical reports

· Requires the ability to motivate, lead, and develop departmental staff from an organizational as well as technical perspective

· Demonstrated ability to work effectively in a team environment, manage multiple priorities, exercise sound judgment, be well organized, take initiative, be flexible, work well under pressure and produce accurate and timely work.

· Fluent in both Chinese and English.

 

企业介绍：www.hansoh.cn

豪森医药创建于1995年7月，现已发展为集化学、生物药物研究，医药中间体、原料药合成、制剂制造和产品销售于一体的创新型医药集团。2011年期末职工总数超过4000人。集团总部及制造基地位于风光秀丽的花果山下、国家级连云港开发区新医药产业园内，在上海、北京设有创新药物研发中心和临床研究中心。豪森医药集团是国家重点高新技术企业和中国制药工业百强企业，综合竞争力、经济效益位居全国同行业前列。
豪森拥有遍布全国的销售网络和专业化的营销团队，专业化的营销模式使豪森品牌的市场价值不断提升，市场规模不断扩大。目前，江苏豪森集团在抗肿瘤、精神、内分泌、抗生素及消化道类等五大疾病治疗领域有40多个品种进入市场销售，2011年销售额近40亿元。