Talent@Boehringer Ingelheim
About Biopharmaceutical Contract Manufacturing
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. 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
-The basic job profile covers mastering all DSP related technologies from of development and optimization tasks for downstream process, including buffer preparation, purification, filtration, and biophysical characterization of the product protein.
-Responsible for transfer from internal or external customers, and preparation of transfers to clinical manufacturing or manufacturing.
-Under the guidance from the supervisor, ensuring timely and cost effective process establishment in development, optimization and scale-up to meet all quality and regulatory demands.
-Working with DoE/QbD tools to enhance development of robust and scalable DSP processes; not only in the DSP process but also including raw material testing and IPC/IPA during the whole process.
-Compiling reports, SOPs and other documentation as well as presentations of results according to timelines.
-Responsible for the production of drug substance applying state of the art technologies to enable reliable clinical supplies according to cGMP.
-Ensuring good communication, material and data handover with internal and external customers and interfaces as upstream development, QC, and transfer partners.
-All of the works include planning, coordinating and performing of work package, and discussing with supervisor and senior scientists. The work result shall be documented, summarized, and presented.
Qualifications
-Education/Degree Requirements: Bachelor or Master above
-Major: Biopharmaceuticals, Biology, Biochemistry, Biotechnology, Bio Engineering
-Language skills& proficiency:Good English in reading, writing and speaking
-Required capabilities (skills, experience, competencies):
-Solid experience in downstream process development and optimization for biomaterials
-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
-Executing for results: Maintains high standards of performance for himself/herself, and follows through on commitments
-Makes timely decisions when a quick response is required and a number of possible alternatives are available