衡阳招聘

Job Purpose and Key Responsibilities 岗位的目的和主要岗位职责:

¨ why job exists / what it must achieve岗位为什么存在 / 岗位必须完成的工作

• To manage project completion and resource planning for a supporting team to ensure all allocated project timescales are effectively and efficiently managed whilst maintaining clear internal and external team communication
• Work with the Project Planner and relevant Work Streams to define project schedule/structure including work and organisation breakdown structures including summary milestones
• Engage key stakeholders (e.g. Engineering, Production, Technical, Quality groups ) to facilitate the necessary actions in order to achieve effective project completion
• Responsible for the application of procedures in relation to QA technical activity
• Manages quality and regulatory compliance requirements during the start up phase adhering to current policies associated with Sterile manufacturing

Accountability 责任:

¨ primary deliverables of role; it's scope; impact on strategy, policy, business or people relationships

责任范围，对公司战略、政策、业务及人际关系的影响程度

• Identify, highlight and communicate challenges to the Program Director in a timely manner
• Updates relevant databases and maintain a central repository for information pertaining to the project and provide regular communication with all stakeholders during the project lifecycle
• Perform peer reviews within PMO team by producing reports, monthly KPI and SLA reports as required and assists in production of communication material for the PMO
• Ensures all quality and regulatory requirements are ‘In Place & In Use’ during the start up of the Cephs facility (commissioning/qualification phase) and transition to the day to day Operations post start up

· Ensure the appropriate level of training is administered across the Cephs facility to ensure full compliance with the QMS

Specialized Knowledge 专业知识:

¨ breadth & depth across disciplines or functions; expertise in field required

所需知识的宽度（跨学科），所需知识的深度 （特定学科）

• BSc/BA, or equivalent level of education, with a minimum of 10 years direct Sterile (aseptic manufacturing) experience
• Working knowledge of current local, provincial and State drug regulations
• Demonstrated ability lead a team of individuals in the study start up process activities
• Has experience of large scale business change projects / programmes
• Ability to work independently, prioritize and work with a matrix team environment is essential
• Strong written and verbal communication skills to express complex ideas to study personnel, internal and sponsor team member (proficient in English is a pre-requisite)
• Excellent organizational and interpersonal skills

GlaxoSmithkline/葛兰素史克
作为世界领先的制药业巨擘，葛兰素史克公司秉承以研究开发为基础的一贯理念，凭藉公司本身的技术潜力和资源优势，在当今瞬息万变的医疗保健领域保持强劲的增长势头。
葛兰素史克公司，由葛兰素威康和史克必成强强联合，于2000年12月成立。两家公司的历史均可追溯至19世纪中叶，各自在一个多世纪的不断创新和数次合并中，在医药领域都确立了世界级的领先地位。两个制药巨人的成功合并，为葛兰素史克成为行业中无可争议的领导者奠定了基础，并在全球药品市场中占据有7%的份额。
葛兰素史克公司总部设在英国，以美国为业务营运中心，在抗感染、中枢神经系统、呼吸和胃肠道/代谢四大医疗领域代表当今世界的最高水平，在疫苗领域雄居行业榜首。此外，公司在消费保健领域也居世界领先地位，主要产品包括非处方药、口腔护理品和营养保健饮料。2006年公司在全球的销售总额达232亿英镑。目前，公司在全球拥有10万余名既掌握专业技能又有奉献精神的出色员工。
全球研发中心有1万6千科学家和技术人员分布在全球许多国家。为进一步推动研发全球化，葛兰素史克(GSK)中国研发中心于2007年6月成立。中心将侧重于神经退行性病变的研究，目标是为多发性硬化病、帕金森病和阿尔茨海默氏病等严重疾病开发新药。中国研发中心将发展成有1000多科学家和技术人员的全球研发中心。中心将以科学研究为基础（science-driven），通过生物学，化学以及最新技术，创新开发新的治疗手段。中国研发中心将最终引领GSK在这一领域从识别药物靶标到后期临床研究的全球研发活动，并在中国和其他研究机构密切合作。GSK中国研发中心计划在未来10年内成长为GSK的大型研发中心之一。
更多信息请访问我们的网站：www.gsk.com or www.gskchina.com