Associate Director, Manufacturing Operations

Job description

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. Bristol Myers Squibb Netherlands Bristol Myers Squibb has been active in the Dutch market for over 50 years, employing people across a range of activities and business units in Utrecht, The Netherlands. The Netherlands is also home to our first European Cell Therapy facility, located at the Leiden Bio Science Park, the largest life sciences cluster of The Netherlands. This new state of the art facility is focused on commercial manufacturing with capabilities for multi-product Cell Therapy manufacturing. You can become part of this exciting journey. Check out this video if you want to know more about it! The Netherlands has everything it takes to become the medicines hub of Europe, the so-called Boston by the North Sea. As we continue to expand our footprint by building this new site, we are looking to grow our team. Would you like to become an important chain in our worldwide network to bring this new personalized treatment to patients suffering from blood cancer? Join us and be a game changer! For more information about Bristol Myers Squibb Netherlands, visit us at bms.com/nl or careers.bms.com/nl Position Summary WORKING CONDITIONS Must be able to work in a cleanroom environment that requires gowning. Work in areas where handling human blood products (Biosafety Level 2) will be required. Must be able to work nights, weekends, and shift structure. This role leads one of the manufacturing operations team at the Multi-Product BMS CT Manufacturing Site in Leiden, NL and will directly report into the Senior Director Manufacturing Leiden Cell Therapy Manufacturing. This role is responsible for oversight and delivery of the manufacturing start-up activities, clinical and commercial GMP manufacturing operations, talent management/succession planning and engagement and retention strategies for Leiden CT Manufacturing Operations. Responsible for identifying and implementing policies, procedures, and manufacturing strategies to facilitate optimal production and performance. Responsibility includes delivering on critical project milestones and managing a functional area that will have a direct impact on the growth and success of the manufacturing facility. This role ensures the safe, validated, and compliant state of processes and procedures and develops appropriate improvement strategies to keep the operational processes with compliance and license guidance. This role is responsible, in collaboration with Manufacturing management, to manage the Manufacturing Operations long term business strategy, business continuity plan, annual department budget, business case creation/evaluation process, portfolio management and Operational Excellence Program. Key Responsibilities Leading one of the BMS CT Manufacturing Operations Teams, in shift, at the Leiden site to include; Hiring, mentoring, and developing exceptional people/teams, conducting performance reviews, and identifying opportunities for career growth for Senior Managers, Managers, and Associates. Leading a team of 5-8 direct report and ~80 indirect reports. Ensuring a culture that embraces safety in the work environment and safety of the patients through compliance with company procedures, policies, and cGMP requirements. Championing a culture of exceptional teamwork, accountability, continuous improvement, and communication across the organization. Provide leadership and oversight in the implementation and execution of manufacturing processes according to established procedures and production records with CGMP’s. Address priorities, meet schedule, maximize productivity, control costs, and increase efficiency. Qualifications & Experience 10+ or more years of experience in pharmaceutical manufacturing operations, manufacturing science and technology, manufacturing systems, and/or quality assurance. 8+ years leadership experience including leading leaders. Strong knowledge of GMP compliance and GMP manufacturing operations. Strong communication skills - both written and verbal communication skills with the ability to translate complex projects requirements and information into plans, improvements and standards. Background in Protein Biologics or Cell Therapy Manufacturing required. Certified Black Belt or equivalent certification (Lean Expert). # LI-Onsite #BMSCART Disclaimer: For any third parties or external agencies, please, be informed we do not accept unsolicited requests, proposals, applications or profiles for any of our roles at BMS. Why You Should Apply We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway. How We Work Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working. Supporting People with Disabilities 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 adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. Candidate Rights BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. For roles based in Los Angeles County only: 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: https://careers.bms.com/california-residents/ Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If this posting is missing required information required by local law or incorrect, contact BMS at TAEnablement@bms.com with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account. R1606308 : Associate Director, Manufacturing Operations