PR&D Head
庄信万丰(烟台)化工产品有限公司
- 公司规模:50-150人
- 公司性质:外资(非欧美)
- 公司行业:石油/化工/矿产/地质
职位信息
- 发布日期:2017-01-04
- 工作地点:烟台
- 招聘人数:1人
- 工作经验:5-7年经验
- 学历要求:硕士
- 语言要求:英语 熟练
- 职位月薪:10000-30000/月
- 职位类别:生物工程/生物制药
职位描述
职位描述:
? Responsible for assigning overall activities of a project and acting as primary client contact.
? Conducts evaluations of requests for proposals of new potential projects and responsible for proposal writing with relevant input from other departments.
? Responsible for directing the activities of a scientific team in the research and/or development of Regular Starting Materials (RSMs), or APIs.
? Responsible for scheduling assigned projects and resources within the group to meet the agreed upon project objectives and financial obligations.
? Works closely with all functions to ensure efficient and timely project deliverables to customers. Develops the project scope and objectives based on the portfolio and corporate initiatives.
? Manage employees on day-to-day basis and implements new procedures, delegates and plans projects, and provides training.
? Provides leadership for employee relations through effective communication, coaching, training, and development, and ensures staff acts in accordance with Johnson Matthey policies and practices with respect to our quality management standard (ISO9001:2008 and possibly GMP), environmental, health, and safety (EH&S) and other related regulatory requirements.
? Advises project teams in areas of scientific, regulatory, project management, client, and safety issues and helps develop capabilities of the group.
? Responsible for monitoring and evaluating the completion of tasks, goals, and objectives of projects. Provides focused feedback to group members to help accomplish project or career goals, performance objectives and annual review.
? Assist in developing and retaining customer relations.
? Provides leadership for problem resolution to facilitate technical improvements and build strong working relationships with Quality Control, Quality Assurance, Analytical Method Development and Production groups.
? Accountable for documentation and reports related to client based process development.
? Other duties as assigned
? BS in organic chemistry or equivalent with a minimum of 15 years related experience in a pharmaceutical industry; MS in organic chemistry or equivalent with a minimum of 10 years related experience in a pharmaceutical industry; Ph.D. in organic chemistry or equivalent with a minimum of 5 years related experience in a pharmaceutical industry
? Minimum of 5-6 years experience with direct API process development in late stage
? Experience with a high level of project management and group management skills
? Experience with business development and client relationships
? Experience in applying and implementing GMP concepts
? Strong written and verbal communication and presentation skills
? Strong technical writing skills and the ability to clearly express ideas in English
? Ability to adapt management style to different personalities
? Ability to positively resolve conflict
? Demonstrate attention-to-detail, problem solving, and ability to make decisions quickly
? Experience with Microsoft Office and other complex computer software
? Experience with developing APIs in late-phase trials
? Strong knowledge of MS Project. Experience in establishing integrated plans with resource and task constraints
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? Responsible for assigning overall activities of a project and acting as primary client contact.
? Conducts evaluations of requests for proposals of new potential projects and responsible for proposal writing with relevant input from other departments.
? Responsible for directing the activities of a scientific team in the research and/or development of Regular Starting Materials (RSMs), or APIs.
? Responsible for scheduling assigned projects and resources within the group to meet the agreed upon project objectives and financial obligations.
? Works closely with all functions to ensure efficient and timely project deliverables to customers. Develops the project scope and objectives based on the portfolio and corporate initiatives.
? Manage employees on day-to-day basis and implements new procedures, delegates and plans projects, and provides training.
? Provides leadership for employee relations through effective communication, coaching, training, and development, and ensures staff acts in accordance with Johnson Matthey policies and practices with respect to our quality management standard (ISO9001:2008 and possibly GMP), environmental, health, and safety (EH&S) and other related regulatory requirements.
? Advises project teams in areas of scientific, regulatory, project management, client, and safety issues and helps develop capabilities of the group.
? Responsible for monitoring and evaluating the completion of tasks, goals, and objectives of projects. Provides focused feedback to group members to help accomplish project or career goals, performance objectives and annual review.
? Assist in developing and retaining customer relations.
? Provides leadership for problem resolution to facilitate technical improvements and build strong working relationships with Quality Control, Quality Assurance, Analytical Method Development and Production groups.
? Accountable for documentation and reports related to client based process development.
? Other duties as assigned
? BS in organic chemistry or equivalent with a minimum of 15 years related experience in a pharmaceutical industry; MS in organic chemistry or equivalent with a minimum of 10 years related experience in a pharmaceutical industry; Ph.D. in organic chemistry or equivalent with a minimum of 5 years related experience in a pharmaceutical industry
? Minimum of 5-6 years experience with direct API process development in late stage
? Experience with a high level of project management and group management skills
? Experience with business development and client relationships
? Experience in applying and implementing GMP concepts
? Strong written and verbal communication and presentation skills
? Strong technical writing skills and the ability to clearly express ideas in English
? Ability to adapt management style to different personalities
? Ability to positively resolve conflict
? Demonstrate attention-to-detail, problem solving, and ability to make decisions quickly
? Experience with Microsoft Office and other complex computer software
? Experience with developing APIs in late-phase trials
? Strong knowledge of MS Project. Experience in establishing integrated plans with resource and task constraints
职能类别: 生物工程/生物制药
公司介绍
成立于2010年的庄信万丰(烟台)化工产品有限公司(原阿法埃莎星马(烟台)化工产品有限公司)是一个生产医药中间体和为生产原料药(API)提供从早期研发到商业化生产全面服务的CRO/CMO公司。庄信万丰(烟台)在2014年通过了ISO9001:2008质量审计认证;同年通过了庄信万丰原料药起始物供应商质量审计成为庄信万丰集团的常规原料药起始物(RSM)供应商。
凭借庄信万丰集团公司在医药服务、手性催化剂技术和原料药等全球业务产业链的优势,依托庄信万丰原料药业务的技术及质量管理体系以及先进的EH&S体系,中国大陆便捷原材料来源和丰富的人才储备,庄信万丰(烟台)能够为欧美、日韩等国家和地区以及中国国内的生物医药客户提供高性价比的个性化定制服务。我们杰出的研发团队能够提供FTE、API对照品及相关杂质的快速合成、路线探索、工艺技术开发及反应参数筛选等相关CRO服务。庄信万丰(烟台)的研发实验室、公斤级实验室及中试车间均按照国际EH&S管理标准装备建成,可实现从克级到百公斤级的全方位定制生产(CMO)服务。
凭借庄信万丰集团公司在医药服务、手性催化剂技术和原料药等全球业务产业链的优势,依托庄信万丰原料药业务的技术及质量管理体系以及先进的EH&S体系,中国大陆便捷原材料来源和丰富的人才储备,庄信万丰(烟台)能够为欧美、日韩等国家和地区以及中国国内的生物医药客户提供高性价比的个性化定制服务。我们杰出的研发团队能够提供FTE、API对照品及相关杂质的快速合成、路线探索、工艺技术开发及反应参数筛选等相关CRO服务。庄信万丰(烟台)的研发实验室、公斤级实验室及中试车间均按照国际EH&S管理标准装备建成,可实现从克级到百公斤级的全方位定制生产(CMO)服务。
联系方式
- 公司地址:上班地址:山东烟台开发区八角无锡路9号