VP

面议

江苏省

刷新时间：2019-10-24

职位描述

Essential Functions:
• Develop product and related technology roadmap to support the Company’s business objectives.
• Build, mentor and assure appropriate management development for key personnel.
• Direct the design and development of new products, including drug substance and drug product manufacturing processes.
• Provide strategic vision and direction to pharmaceutical development through process science, analytical method development, pre-formulation, formulation, product development and characterization programs.
• Conduct due diligence of partner selection for manufacturing, based on knowledge of pharmaceutical facility design, commissioning, validation and operation.
• Provide guidance for non-clinical formulation work, toxicology and clinical feedback into robust dosage forms and processes for IND-related regulatory submissions.
• Prepare and present reports outlining the outcome of technical projects and make recommendations for actions and budget necessary to achieve desired results.
• Participate in meetings with holding company, collaborators, and investors and ensures information communicated is accurate and up to date regarding industry trends and standards.
• Ensure adherence to SOPs, GXPs and worldwide health authority regulations as appropriate, both internally and externally.
• Oversee and manage development budget and headcount.

Preferred Experience and Skills:
• Minimum of 15 years of experience in biotechnology drug development.
• Results-oriented, self-motivated individual with proven leadership and interpersonal skills.
• Demonstrated success in technical proficiency, scientific creativity, team building, external collaboration, and product delivery.
• Experience in intellectual property and patent prosecution.
• In-depth expertise with biologic production processes including developability, cell culture/fermentation, purification, formulation, and lyophilization.
• In-depth expertise in analytical methodology for proteins.
• In-depth expertise in nonclinical development requirements including toxicology and preclinical pharmacology.
• Established reputation in the scientific community as a thought leader with a robust record of publications.
• Ability to meet development goals on aggressive timeliness while having a record of effective collaboration with cross-functional teams.
• Knowledge and experience with FDA and other regulatory bodies and guidelines.
• Excellent teamwork and communication skills.
• Ability to motivate and influence teams to accomplish goals in a dynamic changing organization.
• Expert knowledge of immunology, oncology, analytical biochemistry, or related disciplines.

其他要求

招聘人数：1人
所属部门：生物研发
汇报对象：集团VP
职能类别：分子生物技术

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。