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
Our Associates perform a crucial role in driving our novel cell therapy programs by supporting routine manufacturing operations. We are searching for innovative, intellectually curious individuals with a general understanding of Good Manufacturing Practices (GMPs) to support routine manufacturing operations for Cell Therapy. Successful candidates must be goal-oriented and flexible, with the ability to work effectively and efficiently on a team while demonstrating safety, quality, and GMP compliance at all times.
Duties/Responsibilities:
Execute operations as outlined in Standard Operating Procedures (SOPs) and batch records
Executes transactions and process in all electronic systems
Perform all tasks in a manner consistent with the safety policies, SOPs, quality systems, and GMP requirements
Complete training assignments to ensure the necessary technical skills and knowledge
Train for proficiency in process systems and some supporting business systems
Work within a controlled cleanroom environment and perform aseptic processing (as assigned; maintain manufacturing environmental conditions (Non-Viable Particulate(s) and Viable microbial levels per controlled area classification specifications) by performing area disinfection regiment as required to meet global Health Authority requirements
Able to train new operators
Role models and leaders for the culture of compliance
Controlled document & Deviation authoring, change impact assessment and action owner
Demonstrate a strong practical and theoretical knowledge in their work
Can represent department in cross-functional department collaborations
May before Team Lead duties as needed / delegated
Complete documentation required by governing controlled documents and batch records
Solve complex technical problems; takes new perspectives using existing solutions
Train others on SOPs, Work Instructions to successfully complete manufacturing operations
Qualifications:
Associate or bachelor's degree in related field is preferred.
A minimum high school diploma and/or equivalent combination of education and experience is required.
MBO 3 of 4 in science related field and/or equivalent
Experience:
3+ years of cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience and education
Extensive knowledge of cGMP…