Senior Director, Manufacturing
康日百奥生物科技(苏州)有限公司
- 公司规模:150-500人
- 公司性质:外资(非欧美)
- 公司行业:制药/生物工程
职位信息
- 发布日期:2019-10-16
- 工作地点:苏州-工业园区
- 招聘人数:1人
- 工作经验:无工作经验
- 学历要求:招1人
- 语言要求:不限
- 职位月薪:5-7万/月
- 职位类别:生物工程/生物制药
职位描述
The Senior Director, Manufacturing will lead the building and operation of the manufacturing division for Bioworkshops. The scope of manufacturing encompasses cell culture (USP), purification (DSP, and fill-finish (Filling).
制造部高级总监将领导康日百奥公司生产部的建设和运作。生产范围包括细胞培养(USP)、纯化(DSP)和制剂灌装(Filling)。
Primary responsibility for the Senior Director will be ensuring timely supply of high-quality biological drug substance and finished drug products.高级总监的主要职责将是确保高质量的生物制品原液和成品的及时供应。
Preferred Working Style 首要的工作风格
- Organized leader with strong prioritization and delegation skills;
有组织的领导者,具有很强的优先级和工作分配技能
- Enjoy working in highly structured system to achieve high operational efficiency and consistent product quality;
享受工作于高度结构化的系统中,以实现高运营效率和一致的产品质量
- Excellent communication skills in Chinese and English to accurately exchange highly technical information and persuade diverse audience groups;
优秀的中英文沟通能力,准确交流高技术信息,说服不同的受众群体
- Strong business acumen.
很强的商业头脑
Job Functions工作职责
Management 管理
· Member of the Company’s Senior Management Team;
公司高层管理团队成员
Responsible for commercia operation of manufacturing division.
- 负责商业化生产的日常运营。
Site Safety and Environmental compliance工作场所安全和环境合规
· Develop and maintain a culture of safe working practices through personal leadership and compliance with Company procedures; and
遵守公司安全环保规章制度,身体力行的建立并自觉维护安全工作的企业文化
Manufacturing 生产
Establish and continuously improve manufacturing procedures, processes, and related equipment.
建立并持续改进生产操作步骤、工艺和相关设备。
· Optimize manufacturing output and labor efficiency across varying shift structures while meeting required safety and quality levels;
在满足所需的安全和质量水平的同时,通过轮班结构的优化来提高生产能力和工作效率
· Lead reliable, cost-effective, and efficient operation of the Manufacturing division facilities encompassing drug substance (USP and DSP) and drug product departments to deliver batches of product in compliance with GMP and on time;
领导包括原液(USP和DSP)和成品生产在内的生产车间通过可靠、经济、高效的运作,按时交付符合GMP要求的产品
· Coordinate ordering of starting materials, management of intermediates, and finished products; and
协调原材料采购,中间品管理,成品管理;以及
· Lead close collaboration with other Operations divisions, Quality Unit, and Clients to execute technology transfers.
领导与其他运营部门、质量部门和客户间的紧密合作,执行技术转移工作
Quality Assurance 质量保证
· Represent manufacturing operations at audit by government authorities and Clients;
代表生产部门接受政府部门和客户的审计
· Lead creation of the Company’s policies and procedures related to manufacturing operations;
领导制定公司与生产运营相关的政策和规程
· Comply with Good Manufacturing Practice for the intended countries of product distribution;
遵守产品分销目标国家的GMP规范
Qualifications 任职资格
· B.S. (preferably Biology or Chemistry)
学士学位(优先考虑生物学或化学方向)
· Advanced degree in biological science (Masters or PhD)
生物科学相关高等学位(硕士或博士)
Essential Experience 必要经验
· Minimum of 15 years responsibility in manufacture of therapeutic biologics;
至少15年的治疗性生物制品生产经验
· At least 10 years of operational experience in a regulated biopharmaceutical manufacturer with exposure to facility start-up;
至少有10年在受监管的生物制药企业的运营经验,并有工厂初创经验
· At least 2 years operational experience in manufacturing of mAbs;
至少2年以上单克隆抗体生产操作经验
· Represented manufacturing function at a regulatory inspection by government agencies (NMPA/CFDA, US-FDA, and EMA or similar);
代表生产部门接受政府机构的监管检查(NMPA/CFDA、US-FDA、EMA或类似机构)
· Management responsibility for operation of a biologics manufacturing facility operating at least 2,000L in scale.;
管理过生产规模至少为2000升的生物制品产线
Preferred Experience 优先考虑
· Thorough understanding of MAb development, manufacturing, and analytical process;
对单克隆抗体产品的开发、生产和分析过程具备全面的了解
· Sound understanding of PIC/S guidelines and recommendations;
对PIC/S的指导原则和建议有充分的理解
职能类别:生物工程/生物制药
公司介绍
The Company has recently acquired a 28,000 sq. meter building and land in Suzhou and is investing over RMB300M in building state-of-the art development and clinical manufacturing facilities in 2019 and will be well on the way towards our goal of obtaining the first IND approval in 2020.
康日百奥(苏州)是一家总部位于香港的抗体研发企业,致力于汇同其国际合作伙伴为中国乃至全球带来行业领先和同类之最的新药产品。我们遵照国际标准开发基于细胞培养的生产工艺来进行临床用原液和成品的生产。我们的使命是通过制造科学的专业应用,比中国其他竞争对手更快速的完成生物制品的开发及批准。
我们公司最近在苏州收购了一栋总建筑面积28000平米的大楼及土地,投资了超过3亿元人民币拟在2019年建成具备先进水平的研发和临床样品生产基地并将在2020年实现获得首个IND批准的目标。
Talented, productive experts
极具才华且成果卓著的专业团队
The founding members of Bioworkshops are industrial veterans from Australia and China who have been starting-up and leading biologics product development companies and biologics manufacturing organizations all over the world for more than 20 years. In the past five years alone, the founding team has successfully developed over 10 new antibody products for US, Australia, and China markets and have completed successful design, build, and start-up of four biologics development and manufacturing centers:
Clinical and commercial production.
Inspected for compliance against US-FDA, NMPA, TFDA, and TGA regulations to file CTA/IND and commercial products.
We have quickly established a start-up team and are recruiting more expert staff to exceed 150 employees within the coming year.
康日百奥的创始成员是来自澳大利亚和中国的行业资深人士,在过去20余年的时间里在世界范围内创办并领导了多个生物制品研发及生产企业。仅在过去的五年中,创始团队就成功为美国,澳大利亚和中国市场开发了10多种新型抗体产品,并同时成功完成了四个生物制品研发和制造中心的设计、施工和启用:
临床和商业化生产
通过了美国食品及药物监督管理局,中国药品监督管理局,台湾卫生福利食品药物管理署和澳洲医疗用品监管局针对新药临床申报和药品商业化报产的现场检查
我们已快速的建立起了一支初创团队并将持续的招募更多的专业人士加入以期在明天扩展成为一个规模达150人的团队。
Management of Quality
质量管理
Predictable, excellent performance requires deliberate management of quality with commitment to continuous improvement. Bioworkshops Quality Management System encompasses all business operations with particular focus on pharmaceutical product quality in development and manufacturing to comply with Chinese, European, and American Good Manufacturing Practice.
可预见且卓越的表现需要深入***的质量管理,并致力于在过程中不断的改进。康日百奥的质量管理体系贯穿于公司的整个商业运营过程中,并尤其注重医药产品在研发和生产过程中的质量,以符合中国,欧洲和美国GMP规范。
Innovative R&D Hub and Productive international-standard facilities
创新型研发中心和高产能国际标准厂房
Located within in the heart of Suzhou Industrial Park, we are building high-capacity drug discovery, development and manufacturing facilities for
Development capacity for 8-12 INDs per year.
Clinical drug substance manufacturing to 2,000L.
Aseptic filling of liquid product into vials.
Best in class bioprocess and analytical performance.
我们位于苏州工业园区的核心区域,正在建设大容量的新药发现,开发和生产基地:
建立具备每年开发8-12个IND项目的能力
2000L临床用原液生产
无菌水针制剂灌装
一流的的生物工艺和分析能力
Bioworkshops Founding Values
康日百奥价值观
We believe that strong culture and alignment of purpose are essential in business. The core principles maintained by Bioworkshops are:
Excellence in biologics innovation and development.
Strong relationships based on honesty.
Sustainability measured by workplace safety, impact on the environment, and longevity in business.
Enthusiasm for ambitious goals and creative solutions.
Respect for the sustained effort required to achieve ambitious goals in our industry.
我们相信强有力的文化和共同的目标对于企业至关重要。康日百奥所维系的核心原则是:
卓越的生物制品创新和研发
牢固的关系源自诚信
可持续性通过安全生产,环境影响和长久永续的商业模式来衡量
热衷于树立远大目标并提出创造性解决方案
敬畏那些在本行业中为了实现宏伟目标而持之以恒付出的努力
联系方式
- 公司地址:地址:span东旺路五号