南平 [切换城市] 南平招聘南平生物/制药/医疗器械招聘南平药品生产/质量管理招聘

质量合规专员Quality Compliance Specialist

辉瑞制药有限公司

  • 公司规模:5000-10000人
  • 公司性质:外资(欧美)
  • 公司行业:制药/生物工程

职位信息

  • 发布日期:2017-01-27
  • 工作地点:杭州
  • 招聘人数:若干人
  • 工作经验:3-4年经验
  • 学历要求:本科
  • 语言要求:英语 熟练
  • 职位类别:药品生产/质量管理  

职位描述

职位描述:

主要职责 Responsibilities


根据辉瑞总部的质量目标,执行工厂质量与合规方面的战略目标。
Execute site Quality compliance objective as per Pfizer global quality objective.

建立并实施工厂质量合规管理和预防纠正措施的管理体系,确保工厂的SOP/OI符合cGMP和PQS的要求。关注法规动向,并监督实施法规与公司质量政策/指南的合规性分析,合规行动的制定;
Establish and implement the Site Quality Compliance system and site CAPA management system, to ensure site Procedures/Instructions meet cGMP and PQS requirements. Responsible for regulatory intelligence, and follow up the latest applicable Regulations and PQS update, and monitor the implementation of compliance gap analysis and application system to ensure appropriate actions are defined and tracked to compliance if any gaps are identified.

支持物料管理系统所有人建立并监督物料供应商管理体系的实施,确保根据物料的关键程度和风险大小,就对应的供应商建立相匹配的管控要求,包括但不限于物料认证,供应商的选择,评估,绩效管理,质量协议和变更控制等。
Support Material system owner to establish and supervise the implementation of material supplier management system, to ensure suppliers are managed as per criticality and risk of materials, it includes but not limited to Material Certification, Supplier selection, evaluation, performance management, Quality Agreement and supplier change control etc.

作为质量代表参与工厂的确认/验证工作,确保其符合cGMP和PQS的关于验证的要求。验证相关工作包括但不限于: 制定/审核项目/工厂验证总计划,如设施设备确认计划;监督再验证和设备表现回顾的实施;审核/批准 GMP设施设备相关验证文件和相应SOPs;
Participate site Qualification/Validation activities as Quality representative, to ensure site Qualification/Validation activities meet cGMP and PQS requirements. It includes but not limited to: Develop/review project/site validation master plan, e.g. Utility and equipment qualification plan etc.; Supervise the execution of revalidation and Equipment Performance Review; Review/approve GMP Facilities and equipment related validation/qualification documents and relative SOPs.

维护工厂变更控制体系,监督和协调工厂变更控制流程有效实施,确保所有影响产品质量的变更得到有效的评估和管理。包括但不限于起草/审核/批准相关变更文件,确保根据质量风险评估采取必要的风险控制措施,维护变更系统/数据库。
Maintain site change control system, oversee and coordinate the execution of site change control procedure, to ensure all changes which will potentially impact product quality are appropriate evaluated and effective controlled. It includes but not limited to: Initiate/review/approve change related document; Ensure appropriate action is defined as per risk assessment; maintain Global Change Management System or Local Change Control Database.

执行公司安排的其他相关工作;
Execute any other related work assigned by company;



任职资格 Job Qualification (最低任职要求 Minimum Requirements)


教育程度/经验 Education/Experiences
具有药学,化学或生物相关专业本科学历;具有3年或以上的制药企业质量相关工作经历,熟悉掌握GMP知识及其应用;
Pharmaceutical, Chemical or Biological related Bachelor Degree; No less than 3 years of working experience in Pharmaceutical Quality, and proficient in GMP related knowledges;

特别知识/技能 Specific Knowledge & Skills
生物制药和无菌生产相关GMP知识;
Biologics and Sterile/Aseptic manufacturing related GMP knowledge;
熟练的英语听说读写能力和计算机office软件应用能力;
Proficient in using English as working language at listening, speaking, writing and Proficient in Office application;
熟悉质量合规体系,具备GMP设备确认及工艺验证经验;
Familiar with Quality Compliance system, and have experience in Qualification and Validation;
有效的系统思考能力和沟通技能;有效的组织协调能力和团队协作能力;有效的执行力和达成结果的能力;熟悉掌握分析问题、解决问题以及质量风险管理的理论及其工具。
Fully capable of establishing GMP Quality Management System; Effective Systematical Thinking and Communication ability; Good Coordination and Collaboration; Effective execution and result driving; Good at Problem solving and Quality Risk Management knowledge and Tool application;

职能类别: 药品生产/质量管理

举报 分享

公司介绍

辉瑞公司(Pfizer Inc.)创建于1849年,迄今已有160多年的历史,总部位于美国纽约,是目前全球***的以研发为基础的生物制药公司。辉瑞致力于运用创新的科学技术以及全球资源来改善每个生命阶段的健康和福祉。
我们的目标是“不断创新为患者带来能显著改善其健康的药物”。我们的使命是“成为一家卓越的创新型生物制药公司”。
2012年辉瑞公司全年合计收入590亿美元,研发投入78亿美元。辉瑞在全球拥有9万多名员工,59家生产基地,业务遍及全球150多个国家和地区。2012年财富全球500强企业中辉瑞排名126位。
目前辉瑞公司的产品覆盖了包括化学药物、生物制剂、疫苗、健康药物、动物保健品等用于人类、动物和消费者保健等诸多广泛而极具潜力的治疗及健康领域,同时其卓越的研发和生产能力处于全球领先地位。
在人类和动物药品的发现、开发和生产过程中,辉瑞始终致力于奉行严格的质量、安全和价值标准。每天,分布在世界各地的辉瑞员工致力于促进当地医疗卫生的发展以及探索能够应对当今最为棘手疾病的预防和治疗方案。
辉瑞还与世界各地的医疗卫生专业人士、政府和社区合作,支持世界各地的人们能够获得更为可靠和可承付的医疗卫生服务。这与辉瑞作为一家世界领先的生物制药公司的责任是一致的。160多年来,辉瑞一直努力为人们提供更好、更优质的服务。
辉瑞生物制药目前在华上市的创新药物已超过50个,其治疗领域涵盖了心脑血管及代谢、抗感染、中枢神经、抗炎镇痛、抗肿瘤、泌尿、疫苗及等诸多领域。其中如立普妥®、络活喜®、万艾可®、舒普深®、希舒美®、沛儿®、索坦®许多产品在市场上处于领先地位。为了让中国的广大患者能及时接受与全球同步的先进的药物治疗,辉瑞未来将进一步加大和加快在华新药引进和上市的力度和速度。
辉瑞健康药物旗下的善存®、钙尔奇®、惠菲宁®等消费保健产品也在中国市场家喻户晓,并以其优异的品质深受广大消费者的青睐;辉瑞旗下的硕腾动物保健品*为中国的动物保健市场提供各类领先的动物疫苗和动物药品。

At Pfizer, we apply science and our global resources to improve health and well-being at every stage of life. We strive to set the standard for quality, safety and value in the discovery, development and manufacturing of medicines for people and animals. Our diversified global health care portfolio includes human and animal biologic and small molecule medicines and vaccines, as well as nutritional products of healthcare industry and many of the world's best-known healthcare products such as Centrum. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Consistent with our responsibility as the world's leading biopharmaceutical company, we also collaborate with health care providers, governments and local communities to support and expand access to reliable, affordable health care around the world. For more than 160 years, Pfizer has worked to make a difference for all who rely on us.

联系方式

  • Email:chinahrwest@Pfizer.com
  • 公司地址:南京西路中信泰富