Senior Manager, CAR-T Manufacturing Operations
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 . Job Title : Senior Manager, Liso-cel CAR-T, Manufacturing Operations
Department: Value Stream CAR-T Manufacturing Operations
Location: US-NJ-Summit West, S12 Position Summary:
We are seeking a Senior Manager to oversee a dynamic team of Manufacturing Managers in a 24/7 Cell Therapy operation. The role involves ensuring the execution of key manufacturing processes with a focus on safety, compliance, innovation, and continuous improvement. This position reports to the Associate Director of Manufacturing. Key Responsibilities:
- Leadership & Values: Set an example by leading teams that uphold BMS values of Inclusion, Accountability, Innovation, Urgency, and Passion. Conduct regular 1:1 meetings to mentor and develop the team.
- GMP Compliance: Oversee the manufacturing of cell therapy products in line with cGMP standards and SOPs. Involve yourself in writing and approving SOPs and work instructions.
- Safety & Documentation: Maintain a safety-first culture by conducting safety walks, operating equipment safely, and ensuring meticulous documentation that aligns with ALCOA+ principles.
- Team Development & Building: Recruit, mentor, and assess performance of team members. Create a culture of learning and professional development by addressing deviations and recognizing achievements.
- Deviations & Compliance: Lead deviation reviews, approve records, and ensure timely resolution to prevent recurrence. Engage in CAPA, Change Controls, and relevant projects to enhance process compliance.
- Resource Management: Manage scheduling and resources, adjust priorities to align with business objectives, and provide performance metrics and updates regularly.
- Training: Ensure all team members are trained and compliant with CAR-T GMP manufacturing standards. Maintain 100% on-time training completion.
- Education & Experience: Bachelor's degree preferred; advanced degree a plus. Must have 7+ years of relevant manufacturing experience and at least 5 years in a leadership role with direct reports.
- Skills: Strong knowledge of EHS and cGMPs, ability to manage in a regulated environment, proficiency in biotechnology principles, experience with lean manufacturing (green belt preferred), and excellent communication skills.
- Working Conditions: Comfortable in controlled environments, compliant with safety attire requirements, capable of lifting up to 25 lbs, and able to work around human blood components.
With a single vision as inspiring as Transforming patients' lives through science⢠, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected] . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
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