About the vacancy
Production
Manufacturing Engineering
Process Engineering
(Bio) Process
Manufacturing
Quality Assurance
Oncology & Hematology
About Your Next Job
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.
About Your Next Colleagues
Our employees are passionate about making a difference in patients’ lives. This unwavering commitment gives us a distinct advantage in delivering life-saving treatments to patients, faster.
About Your Tasks and 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.
About Your Skills and Experience
- 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
Where Molecules Meet Opportunities
Mentorship, leadership, growth and inclusion. These are just some of the benefits of a career with BMS.
Contact person
Leanne Macken
At Bristol Myers Squibb, your work helps people prevail over serious diseases. From the scientists behind the microscope to the analysts behind the data, everyone at BMS is working to make an impact. And while our work transforms the lives of patients, it also transforms the lives and careers of our people.
This isn’t easy work, but it is uniquely interesting. You’ll rewrite the rules, solve the toughest challenges, and create miracles.
The BMS Leiden manufacturing facility is our first European site for CAR T cell therapies, joining our global network of facilities transforming care for patients with blood cancer and other serious diseases. Equipped with the latest technology and state-of-the-art production facilities, the facility represents our commitment to ensuring supply of CAR T therapies.