Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

Over het Bedrijf

Bristol Myers Squibb is dedicated to transforming patients’ lives through science, providing a supportive culture that promotes global participation in clinical trials.

De Rol

The Director QC is responsible for QC laboratory operations to ensure timely completion of testing (e.g., drug product, intermediates, stability, raw materials, and microbiology/EM) in compliance with regulatory agencies, cGMPs, and company policies. This role also manages the QC budget and oversees multiple teams within the department.

Verantwoordelijkheden

• Directs QC laboratory to ensure timely completion of testing in compliance with regulations and company policies.
• Defines departmental roles and accountabilities.
• Hires and develops high-quality talent to meet departmental goals.
• Establishes performance objectives for QC staff aligned with business and quality goals.
• Monitors performance measures and provides feedback to foster a collaborative environment.
• Manages lifecycle of analytical methods and technology within the QC laboratory.
• Participates in continuous improvement efforts to drive efficiencies.
• Ensures proper operation and maintenance of laboratory equipment and timely data reporting.
• Participates in regulatory inspections and ensures compliance with BMS policies.
• Responsible for completion of quality records and Annual Product Quality Review.
• Collaborates across teams to harmonize best practices.

Vereisten

• Bachelor’s degree required, preferably in Chemistry, Cell Biology, or related science; advanced degree preferred.
• Minimum of 12 years of relevant work experience required, with at least 6 years in a management role in a cell therapy or biopharmaceutical QC laboratory.
• Advanced knowledge of regulations related to cell therapy products (cGMP, ISO, FDA, etc.).
• Experience with method validation and technical transfer.
• Strong leadership, strategic thinking, and decision-making skills.
• Excellent verbal and written communication skills.

Wat We Bieden

Bristol Myers Squibb offers competitive benefits, services, and programs to support employees in their professional and personal goals.

Sollicitatieproces

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.