VP of Quality

面议

苏州市硕士及以上15年及以上45-55岁

刷新时间：2020-11-09

职位描述

总体职责 / Overall responsibilities
This is a critical position to work at a company level to drive and deliver critical bio-business targets (Time of Delivery, Scope and Quality of Service) by providing excellences in analytics and QC in particularly; collaborating with other departments so as to accomplish the final company (Porton Biologics) goal, to build up successful CDMO business with analytical technologies and QC management and QA management that matches stages of company’s investment and business development.
详细职责 / Specific responsibilities
1. As a member of Porton Biologics Management Team and as a member of PB Portfolio Service Board team.
2. Leads the analytics method development, QC and QA activities in Porton Biologics.
3. Leads own department in accordance with organizational management to fulfill company’s revenue and project goals.
4.Coordinate the work of QA and QC departments to ensure GMP production activities comply with national laws and regulations;
5. Able to prioritize own portfolio, assess opportunities and improve management.
6. Contributes to the operational and strategic managements of Porton Biologics as a whole.
7. Designs routine report on service progress, OKR, KPI, & issues to CEO of Porton Biologics.
8. Assembles, manages, and develops high-performing team (direct reports: Directors/Manages).
9. Participates in necessary Steering Committee Meetings to ensure effective and coordinated interactions among different functions to facilitate the on-time operation of Building 3# and Green-Field project.

任职资格 / Qualifications

学历要求 / Diploma PhD degree in biochemical engineering, biotechnology, biology, or relevant field.

语言要求 / Language Fluent in English and Chinese.

工作经验 / Experience Minimum 15 years of experience in analytics development , quality control and QA of macromolecule at MNC pharma or biotech.
Experience in dealing with US FDA, EMA and NIMPA to ensure our work comply with their expectation.
Proficient in European, American and Chinese GMP implementation requirements.
Experience relating Gene and Cell thereby is a plus.

技术技能 / Technology and Skills
1. Operational excellence: possess the ability to build and lead world class analytics development and quality control facilities of both MAB and GCT nature.
2. Hands-on expert in analytical process development/optimization, qualification, transfer to support clinical and commercial production, including comparability evaluation, formulation and stability studies.
3. Familiar with analytical tech transfer to and from CMO business.
4. Strong leadership/Influence skill.
5. Strong communication skills: able to convey complex concepts and strategies, orally and in writing, and be effective in conducting meetings and making presentation. Have excellent listening skills.

个人品质 / Personality
1. Entrepreneurial spirit: Possess a strong entrepreneurial spirit to make things happen and operate under a fast growth and changing environment.
2. Key relationship: have (and build) personal style, character, and record of achievement to establish credibility with senior management, peers, subordinates, collaborators, partners.
3. Loyal and committed: to demonstrate commitment to the company’s beliefs, values, and organizational goals. Have the utmost integrity and a strong work ethic and be committed to making a positive contribution to the organization.

其他要求

招聘人数：1人
职能类别：质量总监/副总

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。