GMP upstream specialist
职位描述
职位描述:
Basic Purpose of the Position*
岗位的基本目标*
Primary responsibility is operational work on Upstream process (disposable) under GMP conditions for the Biolab and later OASIS, including media preparation, inoculum, fermentation, harvest and IPC analytic.
Coordination and planning of equipment to ensure timely material supply. Ensuring GMP readiness of facility and equipment (e.g. performing of calibration and maintenance). Supporting process transfer activities from internal and external clients.
Oversee daily work package and coordinate work coverage among the team.
Responsible for processing of economic and robust fermentation process for therapeutic proteins and monoclonal antibodies by applying state of the art technologies to ensure manufacturing of bulk drug substance and bulk drug product.
Being part of process transfer teams to secure material supply for projects to support preclinical and clinical studies.
Accountabilities 职责
Perform upstream processing, optimization and scale up to meet all quality and regulatory demands. Carry out preclinical and clinical manufacturing of drug substance under GMP conditions.Handle operational work packages within the team including change-over, scale up, fermentation and in-process controls.
Exchange with colleagues in order to ensure best-practise sharing and best use of resources in accordance with the supervisor
Specialist for fermentation topics, media preparation, inoculum and IPC within GMP requirements. Power user of Single Use Bioreactor and FlexAct (Sartorius) systems as well as other relevant equipment used in BI.
Support trouble shooting and problem solving.
Ensuring good communication, material and data hand over with internal and external customers and interfaces as downstream, QC, R&D and transfer partners.
work within a team of technical and scientific personnel in a complex lab in a disciplined and efficient manner.
Good Documentation Practice in daily work life.
Required Education 所需的教育背景
Bachelor/ Master degree with major in Biopharmaceuticals, Biology, Biochemistry, Biotechnology, and Bioengineering
Required Capabilities (Skills, Experience, Competencies)
所需的能力(技能、经验、胜任能力)
Knowledge about fermentation and upstream processing
Basic knowledge and general understanding of cGMP and documentation according to GMP
Good understanding of organizing a lab
Practical experience with fermentation and related analytical methods (e.g. cell counter, analysis of metabolites)
Basic knowledge of the actually used equipment and systems in BI China, such as disposable bioreactor and FlexAct
Analytical and scientific thinking, clear argumentation and ability to reduce complex issues to the main points
Self confidence
Social competence, customer orientation and team player
This individual will be goal-oriented and focused on meeting deadlines in the required quality within a highly competitive environment
This individual will work hands-on in a cGMP laboratory and also perform cGMP documentation, shift work and week end work will occur on periodic basis
Required Experience
所需的工作经验背景
Basic experience in inoculums, scale-up, fermentation, harvest. Capability to become a highly motivated team player and to move up as a specialist for upstream process.
企业简介
勃林格殷格翰是目前世界上最大、最成功的私人拥有的制药集团。自1885年成立至今,家族拥有的勃林格殷格翰一直致力于研发、生产和营销创新的药品。我们的主要业务包括处方药,消费自主保健药品,生物制药及动物保健。经过百年的发展,勃林格殷格翰的足迹从德国莱茵河畔延伸向全球40多个国家和地区,并成功跻身全球前二十位制药企业之列。
1885年,阿尔伯特.勃林格先生在德国法兰克福附近的殷格翰城创立了勃林格殷格翰公司。
一百多年来,研究与开发驱动着公司的发展。从最初生产酒石酸,乳酸等化工产品开始,到今天许多广为人知药品的推出,勃林格殷格翰公司在研发上的巨额投入使其在呼吸、、心血管、中枢神经、肠胃道等领域拥有优秀的产品,从而赢得有利的市场地位;同时勃林格殷格翰的科学家也数次获得包括诺贝尔奖在内的学术界殊荣。至今公司已在德国、意大利、奥地利、美国、加拿大、阿根廷和日本设立7大研发中心并投入巨资用于新产品的研究与开发。
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上海招聘企业: 百进冠合(海南) 医疗科技有限公司 上海华茂药业有限公司 上海信谊药厂有限公司 上海强生制药 欧姆龙健康医疗(中国)有限公司 青海瑞成药业(集团)有限公司 上海交通大学医学院附属瑞金医院 复旦大学附属中山医院 上海复星医药 上海医药集团
职位发布日期: 2016-12-08