Associate Director, External Manufacturing Quality, Cell Therapy Global Quality
Bristol Myers SquibbChiyoda, Japan
Posted 18h ago
Full Time
About the Company
At Bristol Myers Squibb, we work every day to transform patientsâ lives through science. That work inspires some of the most interesting, meaningful, and life-changing careers youâll experience. Join us and pursue innovative ideas alongside some of the brightest minds in biopharma, collaborating with a team rich in diversity of experiences, and perspectives. We have built a sustainable pipeline of potential therapies and are leveraging translational medicine and data analytics to understand how we can deliver the right medicine to the right patient, at the right time, to achieve the best outcome. Whether in a scientific, business or supporting function, a career at BMS means youâll be inspired every day to grow and thrive through opportunities that are uncommon in scale and scope. Here, youâll be on the cutting edge of powerful innovation in oncology, hematology, immunology, cardiovascular disease, and fibrosis, with colleagues united in the mission to help patients. Through the Bristol Myers Squibb Foundation, we also promote health equity and seek to improve health outcomes of populations disproportionately affected by serious diseases and conditions. Our mission is to give new hope to help patients prevail over serious disease â it drives everything we do. Review our Social Media Community Guidelines at: https://www.bms.com/social-media-community-guidelines.html
Job Description
Bristol Myers Squibb is seeking an Associate Director, External Manufacturing Quality, Cell Therapy Global Quality to provide Quality oversight of Contract Manufacturing Organizations (CMOs) and Contract Testing Labs (CTLs). The successful candidate will have expertise in GCTP/GMP compliance and Japan regulations, with a background in aseptic processing. The role requires strong leadership and communication skills, with experience in Quality Assurance in a commercial manufacturing facility for Biologics or Cell Therapy drug products.
Requirements
- Expertise in GCTP/GMP compliance and Japan regulations
- Background in aseptic processing
- Demonstrated excellence in written and verbal communication in both Japanese and English
- Independent decision-making capability and ability to think conceptually and understand impact of decisions
- Demonstrated ability to work cross-functionally and to develop and maintain strong business partner relationships
- Proven strong leadership, logical thinking and demonstrated ability to engage/influence team in a complex business situation
- Advanced project management capabilities, Six Sigma methodologies, such as process mapping, root cause analysis, and effective problem-solving techniques
Benefits
- Competitive salary and benefits package
- Opportunities for career growth and development
- Collaborative and supportive work environment
- Access to cutting-edge technology and resources
- Recognition and rewards for outstanding performance