Technical Lead 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

Our Technical Lead 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 described in Standard Operating Procedures (SOPs) and batch records

• Lead the matrix FLS (frontline support team) a cross departmental team (QA, QC, F&E, IT, MFG, MSAT, SC&L)

• Responsible for schedule adherence, cycle time and issue resolution. Report variances and communicate/mitigate impact to cross functional groups

• Own deviations and leads investigations / CAPA development

• Qualified as a deviation Lead investigator, responsible for medium and high complex investigations across all manufacturing unit operations.

• Lead investigator (medium and complex investigations > technical, compliance and EHSS investigations)

• Qualified trainer for all GMP operations, closed and open operations, including all grade B aseptic handling.

• Owner of GMP documentation, controlled documents and batch records.

• Responsible for manufacturing operating procedures that are technically sound, promote effective and efficient operations, and comply with cGMP requirements

• Solve complex problems; takes new perspectives using existing solutions. Operational trouble shooting

• Production planning to execute daily unit operations schedule that includes people, product, and material flow across multiple shifts as needed

• 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

• Demonstrate a strong practical and theoretical knowledge in their work and guide team members in issue resolution

• Execute operations described in Standard Operating Procedures (SOPs) and batch records

• Executes transactions and process in all electronic systems

• Demonstrate a strong practical and theoretical knowledge in their work

• Perform 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

• Proficient in process systems and supporting business systems setting up manufacturing areas and equipment/fixtures, as needed

• Collaborate with support groups on recommendations and solving technical problems.

• Ensure the shift works effectively in a team based, cross functional environment to complete all production tasks required by shift schedule

• Collaborate closely with Managers to ensure seamless pass down and communication of operational status

• Completes change actions for change controls or investigations

• Initiates and facilitates triage calls

• Identify and propose innovative solutions

• Drive right first time (RFT) execution of manufacturing unit operations by providing direct training, guidance, and problem solving

• Aid in daily work coordination and distribution as demanded through the production schedule

• Ensure shift notes and hand over communication is complete and accurate, as needed

• Leads Tier 1 and Tier 2 meetings

• Delegate for manager

• Drives positive attitude in team

Qualifications/Education/Experience/Licenses/Certifications:

• 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.

• Netherlands

• MBO 3 of 4 in science related field and/or equivalent 4+ years of cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience and education

• Extensive knowledge of cGMP regulations and FDA guidance applicable to 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.

WORKING CONDITIONS

• Must be able to stand/walk for extended periods of time

• Must be able to work in a cleanroom environment and perform aseptic processing in ISO 5 biosafety cabinets, which require gowning and personal protective equipment (PPE), including by not limited to: safety shoes, safety glasses, aprons, face shields, powered air purifying respirators (PAPR), lab coats, full body gowns, hairnets, gloves, and hearing protection

• Required to carry and/or lift up to 30 pounds / 15 kg, several times a day, while handling production equipment and/or materials

• Required to push and/or pull up to 50 pounds / 15 kg, several times a day, while handling production equipment and/or materials

• Work in areas that may have strong magnets

• Must be able to work in a BSL2/ML1 work environment handling human blood components

• Work in areas with exposure to vapor phase liquid nitrogen

• Must be able to work assigned shift (Day, Evening, Night,

• Weekends and/or Holidays)This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.

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Disclaimer: For any third parties or external agencies, please, be informed we do not accept unsolicited requests, proposals, applications or profiles for any of our roles at BMS.

Why You Should Apply

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.

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 athttps://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/

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