Associate QC Manager
About Animal Health Business
As the leading animal health company in China, we have extensive business coverage from the full value chain in R&D, production to sales and a diversified product portfolio covering swine, poultry, pets, cattle vaccines and medicines. We are always "in China and for China". We've pioneered many game-changers in the veterinary medicine, and we're looking to our customers' needs to guide us into the future.
Responsibility：
- Plan, schedule, coordinate and approve in a timely manner the tests conducted within the respective lab. Responsible for operation and management of Virus lab.
- Provide technical training and support to the team. Evaluate opportunities for improvement and provide corrective action through SOP/GMP/technical training for laboratory staff.
- Lead OOS/OOT and deviation investigation occurred in virus lab and responsible for reviewing, approving related CAPA/Change and ensure the implement of CAPA/Change in the lab.
- Train and supervise technician and evaluate testing methods continuously to ensure test methods are run/executed in a scientific and efficient manner.
- Responsible for assay transfer from Boehringer Ingelheim other sites or R&D units.
- Responsible for stability management and conducting the trend analysis.
- Responsible for the validation management of virus-related equipment and providing timely guidance to subordinates to complete relevant validation.
- Responsible for the validation management of virus-related method and providing timely guidance to subordinates to complete relevant validation.
- Responsible for preparing ,reviewing and approve SOP，TR and the other related document to assure that all procedures used within the laboratory are current and in compliance.
- Maintain a clean and tidy work area whilst complying with quality and EHS requirements. Pay attention to their own safety and the safety of others, no LTA accident.
Requirments：
- Veterinary，Biochemistry, Virology, microbiology education background
- Bachelor's degree or above is preferred。
- At least 2 years of experience in GMP areas and on team management.
- With more than 2 years working experience on cell culture, virology tests, molecular biological tests or related bio-assays。
- Ability to lead the group in technical trouble shooting, develop bio-assay methods and corporate with process team to optimize vaccine manufacturing process.
- Has good learning capability, communication and interpersonal skills。
- Having a team spirit, good sense of responsibility, honesty, integrity, and adherence to principles。