职位描述
Talent@Boehringer Ingelheim
About Boehringer Ingelheim
Join Boehringer Ingelheim and be part of a legacy where your growth is just as important as ours. A global, research-driven pharmaceutical company, we are one of the world’s top 20 leading pharmaceutical companies and have collaborated and innovated medicines in Human Pharma, Animal Health and Biopharmaceutical everywhere in the world for over 130 years. This is your chance to create ‘Value through Innovation’ with our internal and external partners to improve lives around the world, explore new scientific breakthroughs to stay at the forefront of our industry, and become a leader for future generations.
We continue to grow fast and are one of the top growing companies in the industry in China. Join us and be part of our continued journey to grow and achieve BI global Ambition 2025:
? No. 1 in Animal Health
? No. 1 in Biopharmaceutical Contract Manufacturing
? No. 1 in value share for our brands in One Human Pharma
As a leading company, Boehringer Ingelheim thrives on passion, innovation and independence, and offers fulfilling work and growing opportunities to highly dedicated people. Certified as Top Employer in China in the past 5 continuous years, we help our people grow towards their success through high quality career development programmes and opportunities to lead international projects to develop into a leader of tomorrow. At the end of the day, your growth is our growth and vice versa.
For more information, please
1. visit https://www.boehringer-ingelheim.com/ or
2. follow us on LinkedIn, or
3. follow us on WeChat – JoinBI
About Biopharmaceutical Contract Manufacturing
As one of the world’s largest biopharmaceutical producers, Boehringer Ingelheim aims to become China’s first international provider of biopharmaceutical contract manufacturing solutions with all-round services to its clients in China and all over the world. The Company launched its world-class Biopharmaceuticals Manufacturing Site in China in 2017 with first-phase investment of more than EUR 70 million. This site is the first and only biopharma site in line with global standards set by a multinational pharma company in China, and has become a major milestone in Boehringer Ingelheim’s strategic blueprint for its biopharma business globally.
As the leader in biopharma CMO manufacturing, Boehringer Ingelheim introduces innovative business models into China to further promote development of China’s biopharma industry, boosting global competitiveness of Chinese biopharma companies, and facilitating clinical research and market launch of China’s innovative medicines in a bid to accelerate growth of China’s bio-technology industry. The Company’s state-of-the-art production platform, management system and global biopharma network will help bio-medicines made by Chinese companies to enter the global markets.
Job Responsibilities
Primary responsibility is operational work on Upstream process (disposable) under GMP conditions for OASIS, mainly focusing on media preparation applying state of the art technologies for clinical andcommercial supplies according to cGMP.
Coordination and planning of equipment to ensure timely material supply. Ensuring GMP readiness of facility and equipment (e.g. performing of calibration and maintenance).
Responsible for preparation of economic and robust media, buffer and stock solution to support manufacturing of bulk drug substance and bulk drug product.
Perform upstream media preparation, support process optimization and scale up to meet all quality and regulatory demands. Ensure safe processing and safe handling.
Handle operational work packages within the team including change-over, scale up.
Exchange with colleagues in order to ensure best-practise sharing and best use of resources in accordance with the supervisor.
Specialist for media preparation and raw materials within GMP requirements. Understand their impact on cell culture process. Power user of 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 Cell culture, downstream, QC, QA 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.
Support of providing GMP related documents (e.g. SOP, batch record writing, Investigation, CAPA, Change control).
Qualifications
Education/Degree Requirements: Bachelor
Major: Biopharmaceuticals, Biology, Biochemistry, Biotechnology, Bioengineering, Chemistry
Language skills & proficiency: Chinese fluent, English good in written and spoken communication
Required professional certificates / licences: none
Required capabilities (skills, experience, competencies):
Knowledge about media preparation
Good understanding of cGMP and documentation according to GMP
Good understanding of organizing a lab
Practical experience with media preparation for Upstream process and related analytical methods (e.g. osmometer, pH meter, conductivity)
Basic knowledge of the actually used equipment and systems in BI China, such as 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 weekend work will occur on periodic basis
Behaviours
Accountabilities-Even in ambiguous circumstances, always demonstrate ownership for decisions and actions
Agility-Quickly act with an open mind to face internal and external transformation
Intrapreneurship-Together with customers, come up with innovative ideasto respond to changing markets
Contact Us
If you think you can convince us that you are the right candidate we are looking for, apply now！
