職位描述
職位描述：
Basic Purpose of the Position*
1. 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.
2. Coordination and planning of equipment to ensure timely material supply. Ensuring GMP readiness of facility and equipment (e.g. performing of calibration and maintenance).
3. Supporting process transfer activities from internal and external clients.
4. Oversee daily work package and coordinate work coverage among the team.
5. 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.
6. Being part of process transfer teams to secure material supply for projects to support preclinical and clinical studies.
Accountabilities*
1. 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.
2. Handle operational work packages within the team including change-over, scale up, fermentation and in-process controls.
3. Exchange actively with colleagues in order to ensure best-practise sharing and best use of resources in accordance with the supervisor
4. 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.
5. 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.
6. Good Documentation Practice in daily work life.
7. Potentially train new employees and become functional leader for working groups/ tasks.
Qualifications*
1. Bachelor/Master in Biopharmaceuticals, Biology, Biochemistry, Biotechnology, Bioengineering
2. 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.
3. Experience in fermentation and upstream processing with good risk awareness
4. Basic knowledge and general understanding of cGMP and documentation according to GMP
5. Good understanding and practical experience in organizing a lab
6. Practical experience with fermentation and related analytical methods (e.g. cell counter, analysis of metabolites)
7. Basic knowledge of the actually used equipment and systems in BI China, such as disposable bioreactor and FlexAct
8. Analytical and scientific thinking, clear argumentation and ability to reduce complex issues to the main points
9. Self confidence
10. Social competence, customer orientation and team player
11. Good command of English
Other Skills
1. We are looking for person who offers relevant operational experience in process development, and manufacturing experience within a biopharmaceutical company
2. This individual will be goal-oriented and focused on meeting deadlines in the required quality within a highly competitive environment
3. 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
如需申請(qǐng)本職位，請(qǐng)復(fù)制以下網(wǎng)址到您的網(wǎng)頁(yè)瀏覽器 (Please copy & paste the following link to your browser and login to BI job portal for job application):
https://tas-boehringer.taleo.net/careersection/global+template+career+section+28external29/jobdetail.ftl?job=1610504
