GMP upstream specialist
職位描述
職位描述:
Basic Purpose of the Position*
崗位的基本目標*
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 職責
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、經驗、勝任能力)
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
所需的工作經驗背景
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.
企業簡介
勃林格殷格翰是目前世界上最大、最成功的私人擁有的制藥集團。自1885年成立至今,家族擁有的勃林格殷格翰一直致力于研發、生產和營銷創新的藥品。我們的主要業務包括處方藥,消費自主保健藥品,生物制藥及動物保健。經過百年的發展,勃林格殷格翰的足跡從德國萊茵河畔延伸向全球40多個國家和地區,并成功躋身全球前二十位制藥企業之列。
1885年,阿爾伯特.勃林格先生在德國法蘭克福附近的殷格翰城創立了勃林格殷格翰公司。
一百多年來,研究與開發驅動著公司的發展。從最初生產酒石酸,乳酸等化工產品開始,到今天許多廣為人知藥品的推出,勃林格殷格翰公司在研發上的巨額投入使其在呼吸、、心血管、中樞神經、腸胃道等領域擁有優秀的產品,從而贏得有利的市場地位;同時勃林格殷格翰的科學家也數次獲得包括諾貝爾獎在內的學術界殊榮。至今公司已在德國、意大利、奧地利、美國、加拿大、阿根廷和日本設立7大研發中心并投入巨資用于新產品的研究與開發。
熱門區域招聘: 重慶 北京 上海 浙江 江蘇 廣東 山東 湖南 安徽 河北
上海招聘企業: 百進冠合(海南) 醫療科技有限公司 上海華茂藥業有限公司 上海信誼藥廠有限公司 上海強生制藥 歐姆龍健康醫療(中國)有限公司 青海瑞成藥業(集團)有限公司 上海交通大學醫學院附屬瑞金醫院 復旦大學附屬中山醫院 上海復星醫藥 上海醫藥集團
職位發布日期: 2016-12-08