Bristol Myers Squibb zoekt een

Process Engineer

Leiden, Netherlands

Job Description

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 rich in diversity. 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: .

The MSAT Process Engineer is responsible for supporting the production of CAR-T products for both global clinical trials and commercial supply.  Serves as process SME. Collaborates with SME s from the Development, Manufacturing, and Quality while providing technical support for the resolution of process deviations, the evaluation and implementation of process changes and continuous improvement support to the production operations to ensure rapid, flawless, compliant, and cost-effective delivery of quality products

REQUIRED COMPETENCIES:  Knowledge, Skills, and Abilities:

  • Expert knowledge of cGMP’s and multi-national biopharmaceutical/cell therapy regulations

  • Deep knowledge of facility/clean room design, process, equipment, automation

  • Hands-on experience with single-use technologies, closed systems, and cold chain/cryogenic technologies

  • Experience working with external parties and/or leading cross-functional teams

  • Possess strong verbal/written communication skills and ability to influence at all levels

  • Ability to think strategically and to translate strategy into actions

  • Ability to prioritize and provide clear direction to team members in a highly dynamic environment

Education and Experience:

  • Experience with the start-up, process transfer and set up of the new manufacturing facilities

  • Bachelor’s Degree in science or engineering (advanced degree is preferred)

  • 5 or more years of manufacturing support or related experience in the biopharmaceutical industry


  • Interface with operators and serve as process SME.

  • Continuously monitor, analyze, and optimize the end-to-end process and anticipate and permanently resolve issues that may arise during production

  • Provide technical input and investigation support for production related investigations, ensuring compliance with internal standards and regulatory requirements

  • Design and execute test plans and other risk mitigation exercise as part of investigations (e.g. Root cause analysis and CAPAs)

  • Sponsor and support the change initiatives and the implementation of process improvement initiatives

  • Work closely with Engineering /Maintenance on the design and implementation of new technology and new systems/facilities related to production process needs

  • Review and revise the content of technical documentation (e.g. investigations, changes, SOPs and batch records)

  • Interact with other teams including Validation, Development, Operations, QA and Regulatory

  • Lead project teams, prepare project schedules, coordinate the execution of technical projects and develop presentations to disseminate results to project stakeholders and senior management

  • Might need to work in shifts

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

BMS is dedicated to ensuring that people with disabilities can perform complex functions through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit eeo -accessibility to access our complete Equal Employment Opportunity statement.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

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