Associate II Manufacturing, Cell Therapy

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

We will be recruiting 23 people for this role.

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:

Learn and execute Cell Therapy Manufacturing operations

Perform patient process unit operations and support operations described in standard operating procedures and batch records

Executes transactions and process in all electronic systems

Prioritizes safety of self and others

Reports safety events within 24 hours

Escalates any/all issues that may impact safety of self and/or others.

Complete documentation required by governing controlled documents and batch records

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

Trains for proficiency in process systems and some supporting business systems

Execute daily unit operations schedule, that includes people, product, and material flow across multiple shifts

Work within a controlled cleanroom environment and execute aseptic processing procedures (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

Continues to refine and improve manufacturing process technique to improve individual operational times.

Ensures training completion prior to production

Demonstrate strong practical and theoretical knowledge

Collaborate with support groups on recommendations and solving technical and operational problems

Train others on SOPs and 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:

1+ years of cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience and education

Extensive knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing

Peer-level on the floor leadership experience which demonstrates proficiency and compliant schedule adherence is highly desired

Demonstrated aptitude for engineering principles and manufacturing systems

Demonstrated proficiency in common computer tools such as word processing, spreadsheet and web-based applications

Demonstrated good interpersonal skills, is attentive and approachable

Maintain a professional and productive relationship with area management and co-workers

Preferred Experience:

Experience in cell therapy manufacturing, including Cell washing processes and automated equipment. Cell separation techniques and automated equipment. Cryopreservation processes and equipment.

Cell expansion using incubators and single use bioreactors

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.

R1594897 : Associate II Manufacturing, Cell Therapy