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Senior Manager II, Manufacturing Operations, Cell Theraphy

Bristol Myers Squibb

Leiden
Full-time
5-10 years experience
On-site

Key Skills

Manufacturing operations
Process improvement
Data analysis
Troubleshooting
Labeling operations
Quality compliance
Resource utilization
Cost reduction
Risk management
Engineering controls
Procedural controls
Vendor management
Cell therapy
Operational requirements

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.


Key Responsibilities:

  • Identifies key process indicators and collects data to recommend manufacturing and yield improvements.
  • Leads and supports troubleshooting activities to minimize process downtime or re-occurrence.
  • Manages continuous improvement initiatives to enhance labeling operations efficiency, quality and compliance.
  • Monitors resource utilization and identifies opportunities for optimization and cost reduction.
  • Maintains focus on continuous reduction of risk to patient through deploying engineering and procedural controls while delivering operational requirements.
  • Communicates and tracks critical component issues and partners with vendors for resolution.

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 [email protected]. 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 [email protected] 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.



R1606312 : Senior Manager II, Manufacturing Operations, Cell Theraphy

Core Responsibilities

The Senior Manager will identify process indicators to recommend manufacturing improvements and lead troubleshooting activities to minimize downtime. They will also manage continuous improvement initiatives to enhance labeling efficiency, quality, and compliance while optimizing resource utilization.

Requirements

The role requires a focus on continuous risk reduction through engineering and procedural controls. Candidates must be able to communicate critical component issues and partner effectively with vendors for resolution.

Benefits

  • Comprehensive benefits
  • Inclusion
  • Wellbeing
  • Flexibility

About Bristol Myers Squibb

Industry: Pharmaceutical Manufacturing

Company size: 10,001+ employees

At Bristol Myers Squibb, we work every day to transform patients’ lives through science. That work inspires some of the most interesting, meaningful, and life-changing careers you’ll 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 you’ll be inspired every day to grow and thrive through opportunities that are uncommon in scale and scope. Here, you’ll 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 – it drives everything we do. Review our Social Media Community Guidelines at: https://www.bms.com/social-media-community-guidelines.html

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