Production Flow Manager
About Human Pharmaceutical Business
With global presence, Boehringer Ingelheim has industry-leading expertise in medicine research and development. We are constantly developing the next generation of medical breakthroughs and successfully delivering innovations to meet the medical needs of the patients we serve in the following key areas of interest: cardiovascular, respiratory, metabolic diseases, immunology, oncology and central nervous system. In the future, the company will launch new medicines or indications in therapeutic areas including CV & metabolism, respiratory, oncology, immunology, CNS and retinal health to meet the demand of Chinese patients.
Job Responsibilities:
-Work out the flow development strategy and lead the whole flow to achieve compliance, EHS, quality, supply and cost targets.
-Manage the production activities which related to finance performance to make continuous improvement on cost saving to achieve relevant finance target.
-Involve in personnel management, such as performance review, merit increase, personnel change. Establishes sub-function's business and operational plans as well as implements policies and strategies.
-Engage, Enable and Empower the whole production department to case cade down our company Vision, Mission, Value, and cultivate Ethic& compliance, safety, quality, Lead & Learn , Innovation, Diversity & Inclusion and Catalyst leadership culture.
-Lead all flows including solid, liquid and other dosage forms to make continuous improvement on all production process EHS, Quality, Supply and Cost. Implement the Company strategy in the whole production department.
-Ensure all production activities in line with quality & regulatory requirements.
-Approve production related procedures and ensure these procedure being followed strictly.
-Ensure products being produced and stored according to approved technological procedure, ensure the quality of products.
-Ensure the establishment and implementation of quality management system and relevant management regulations for data integrity
-Accountable for the immediate report, investigation and follow up action of any data integrity issue occurring within areas of responsibility
Requirements：
-6+ years related experience with a master's degree or 8+ years with a Bachelor's degree; In which, 3+ years management experience is required
-Pharmaceutical or related majors preferred
-Clear understanding of the regulatory requirements of the Pharmaceutical Industry including a good working knowledge of GMP standards, validation, supply chain processes and relevant EHS requirements
-Be good at cross-function communication and coordination.
-Team player and cross-function leadership
-Fluent in English & Chinese