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制剂副总监/总监

面议

市辖区博士及以上

刷新时间:2021-06-10

职位描述

Role Purpose Statement (how does the role impact business achievements?):

The incumbent will support and lead new product development by developing formulations and/or providing analysis and evaluation of material and products at all stages of the development process, considering scientific and timing objectives. This individual would have various levels of involvement and leadership in the product design and formulation and process development of conventional and non-conventional ointment, cream and other formulations.

Main Accountabilities

1.Responsible for design and execution of proof-of-concept studies, formulation development, manufacturing process development and optimization;

2.Lead pre-clinical and clinical formulation development;

3.Oversee tech transfer and validation of drug product manufacturing processes, and manage CROs in reviewing batch records and specification;

4.Effectively involves or leads in every stage of activities including preformulation, prototyping formulation and/or new dosage form development, new process development and technical transfer to manufacturing site via close collaboration with CMC Head or CROs;  

5.Independently design experiments and carries out scientific work with an awareness of state-of-the-art technology to make the decision based on expertise and technical knowledge. Creates research and development plans to fit overall project objectives under rapidly changing circumstances.

6.Ensure all work is conducted in accordance with written procedures (e.g. quality and safety), methods & batch documents, etc.

7.Identify, challenge, develop and implement written procedures (e.g. quality and safety)

8.Produce or Lead departmental quality documentation (including SOP’s, batch documentation, validation protocols & reports, formulation risk assessment).

Role related Qualifications/ Skills:

1.Work experience:PhD in pharmaceutical sciences with NLT 2 years of industrial or postdoctorial experience in topical product development or innovation drug delivery systems.

2.Good understanding of CH / FMCG product development process and regulatory requirements.

3.Demonstrated success of formulation and/or development of products, preferably topical products.

4.Demonstrated ability to take initiative, think and work independently, problem-solve, work effectively in teams, and multitask.

5.Ability to apply scientific principles and techniques, creativity and innovation to assigned projects.

6.Ability to connect consumer needs to product development.

7.Basic understanding of statistics and its application to experimental work.

8.Ability to organise and report study data from internal and external sources.

9.Ability to communicate problems / challenges and solutions in a clear and concise manner in a complex, matrix environment.

10.Fluent in oral and written English.

其他要求

  • 1人
  • CMC Head
  • 药物制剂

公司介绍

诗迈医药猎头是一家专业从事医药行业猎头服务的科技型企业,总部位于杭州,下属有上海、南京、广州、武汉等多家分公司,同时自主开发国内领先的猎头办公系统及医药人才网站,全面致力于海内外制药、生物、医疗、器械等行业线上线下人力资源整合。
公司与全国各地研发企业、生产企业及销售经营等企业及业内同行建立了良好互动平台,在欧、美、日等国家建立了海归引进平台,同时积极开展医药高等院校公益系列讲座,搭建了以人力、企业为主体的立体化咨询服务网,为医药企业人才队伍建设发挥了积极重要作用,为很多医药企业解决了高端人力之困。

所在城市:
所任职位:
经理M

企业信息

名称:
某高潜biotech
行业:
制药.生物
性质:
外商独营/外企办事处
规模:
50-99人

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