×
Register Here to Apply for Jobs or Post Jobs. X

Senior Manager, Manufacturing, Cell Therapy

Job in 2300, Leiden, South Holland, Netherlands
Listing for: Qabird
Full Time position
Listed on 2026-08-09
Job specializations:
  • Manufacturing / Production
    Operations Management
Salary/Wage Range or Industry Benchmark: 140000 - 190000 EUR Yearly EUR 140000.00 190000.00 YEAR
Job Description & How to Apply Below

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:

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  or

Position Summary

The Manufacturing Operations Sr. Manager leads a team (or multiple teams) that execute the cell therapy anufacturing process. Team scope is organized around cell therapy manufacturing unit operations such as media, kitting, selection, activation or harvest which are executed in accordance with Current Good Manufacturing Practices (cGMP’s) in both a clinical and commercial setting. The Manufacturing Operations Sr. Manager is responsible for managing all aspects of the manufacturing unit operation team including the people written procedures, patient and intermediate materials, equipment and environment of the production area.

Additionally, the Manufacturing Operations Sr. Manager, sponsors complex projects or systems, and helps develop future state business processes for manufacturing.

Duties/Responsibilities
  • Establishing department goals, tracking and reporting KPIs, and driving continuous improvement efforts.
  • Head of Emergency Response team, leading the team leads of the Emergency response teams of multiple departments (QC, W&SC, F&E, MFG and offices) during emergencies and drills.
  • Authorized to order the evacuation of the building and stop operations.
  • First point of contact in case of accidents and emergencies
  • Owner of manufacturing unit operations, including equipment ownership, data analytics, procedures, MES recipes, training content owner.
  • Lead resources scheduling in a matrix organization
    • Designing and operating manufacturing systems that are technically sound, promoting effective and efficient operations, and complying with cGMP requirements
  • Ensuring the schedules of the people, facility, equipment, materials, and documents are established and maintained to support the capacity/throughput of the facility
  • Identifying and mitigating risks in manufacturing operations that could negatively impact delivery of safe and effective therapies to patients.
  • Championing inspection readiness efforts.
  • Establishing team policies, organizational structure, shift structure, and career ladders.
Qualifications
  • 10+ years of experience in cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience.
  • Must have minimum of 5+ years leading a team.
  • Cell…
Position Requirements
10+ Years work experience
Note that applications are not being accepted from your jurisdiction for this job currently via this jobsite. Candidate preferences are the decision of the Employer or Recruiting Agent, and are controlled by them alone.
To Search, View & Apply for jobs on this site that accept applications from your location or country, tap here to make a Search:
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary