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工艺研发负责人 PR&D Head

面议

烟台市博士及以上

刷新时间:2017-07-27

职位描述

Job Objectives
Manage the day-to-day activities of a process research and development group comprised of a team ranging from entry level chemist to experienced chemist. This position is responsible for providing a framework for ensuring continuous improvement in customer satisfaction, project execution, related regulatory compliance, and operational safety and efficiency of the group. Ensures projects are on target with quantity, quality, time, and within budget. Conduct technical evaluations for potential new projects and performs evaluations on the status of current projects. Sets goals and objectives for, and provides mentorship through focused feedback to group members regarding overall performance. Develop new business opportunities through interaction with current or potential clients.
Main Responsibilities
Lab responsibilities
? Responsible for assigning overall activities of a project and acting as primary client contact.
? Responsible for directing the activities of a scientific team in the research and/or development of Regular Starting Materials (RSMs).
? Conducts evaluations of requests for proposals of new potential projects.
? 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 and objectives.
? 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
1.

Quality/Regulatory responsibilities
? Manages staff in full compliance with ISO9001 requirements.
? Responsible for departmental audit readiness and for participating in quality audits with Regulatory Agencies and customers.
? Ensures staff acts in accordance with Johnson Matthey quality policies and practices with respect to ISO9001 and other related requirements.
? Implements and applies ISO9001 concepts in association with department specific responsibilities.
? Demonstrates technical expertise and self-assuredness in applying ISO9001 standards.
EHS responsibilities
? Manages staff in full compliance with all appropriate EHS policies and procedures.
? Responsible for departmental audit readiness and for participating in audits with internal Company groups, regulatory agencies, and customers.
? Ensures staff acts in accordance with EHS policies, practices and procedures. Addresses staff issues accordingly if there are EHS violations.
? Actively participates in root cause investigations on near misses and all incidents. Once identified, ensures corrective actions take place and compliance with Company policies and procedures, and all national regulations occurs within the responsible department.
? Manages compliance with national and local regulations.
? Implements, applies and places emphasis on EHS concepts with department specific responsibilities.
? Demonstrated technical and procedural expertise and self-assuredness in applying EH&S policies and procedures.
? Support the Company’s commitment for environmental health & safety by applying ISO 9001 and Sustainability 2017 principals into daily activities

Requirements:
? 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
? 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

其他要求

  • 1人
  • PR&D
  • 总经理 GM
  • 研发注册

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:
猎头顾问C

企业信息

名称:
诗迈医药猎头
行业:
制药.生物
性质:
私营/民营企业
规模:
100-499人

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