Bristol Myers Squibb

Jobid=4eb18d25bda9 (0.101)

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. Take your career farther than you thought possible.

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. 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!

Position Summary

The Director, Facilities & Engineering (F&E) provides leadership and oversight to Engineering, Maintenance & Reliability, Calibration/Metrology, Qualification/Validation and Facilities Services for the Leiden Cell Therapy facilities.

The core responsibility of the Director of F&E is to ensure a validated and compliant state of operation for systems and equipment, generation and delivery of utilities at peak efficiency, keeping our facilities in a state of compliance, as well as ensuring customer satisfaction by providing facilities management services to fulfill requirements.

Key Responsibilities

Directs all components of the F&E organization, which includes: Facilities, Engineering, Maintenance, Calibration and Metrology, CQV, Capital Project and the IFM partner/s for the Leiden cell therapy site.

Sets high standards, monitors and implements improvements for safety for F&E work and for the facility.

Sets high standards for compliance to meet and exceed regulatory agency requirements related to Cell Therapy manufacture facility and assure compliance with BMS Directives including staff training, cGMP, quality systems documentation, change control, operational variance, and failure investigation.

Ensure reliable, predictable, and compliant operation of all critical facilities, utilities, and equipment to enable uninterrupted GMP manufacturing and patient supply, by proactively preventing failures, strengthening preventive and predictive maintenance, and embedding reliability as a core capability within the F&E organization.

Develops and leads a high-performance management team responsible for operating and maintaining an audit-ready facility at all times; directs the recruitment and development of all F&E staff.

Directs the monitoring and management of outcomes for services performed by contracted business partners, in coordination with global services (Facilities and Engineering).

Develops annual operating budget/staffing levels, manages operations to achieve them and proactively looks for opportunities to reduce costs.

Directs the management of the sites’ future requirements for, and fulfilment performance of, locally provided contract services.

Directs the planning and coordination of the capital projects for the Leiden cell therapy Site, including the development and implementation of the strategic plan, capital spending plan and site master plan.

Reporting Relationship Reporting to the Leiden Site head

Qualifications & Experience

Knowledge of science/engineering generally attained through studied resulting in a B.S. in engineering, a related discipline or its equivalent. A master’s degree in a relevant discipline is desired.

A minimum of 10-15+ years of experience in engineering field or equivalent, preferably in a biopharma manufacturing complex, documented by a solid history of technical accomplishments and a proven track in maintenance, reliability, facility/utilities operations, validation and capital project management.

A strong practical knowledge of process equipment and the technologies related to cell culture manufacturing and both clinical and commercial production.

Experience in directing the design and construction of major office, laboratory and process manufacturing buildings including design, procurement and contracts, including experience in the negotiations and structures of contracts and major agreements.

Proficiency in developing and managing departmental budgets to successfully meet organizational commitments within operating budget guidelines, including the development and implementation of capital spending plans

#LI-Hybrid

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.

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 a supportive culture, promoting global participation 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

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

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 . Visit to access our complete Equal Employment Opportunity statement.

Candidate Rights

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

Data Protection

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

R1599871 : Director, Facility and Engineering

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Director, Facility and Engineering – Bristol Myers Squibb – Leiden

Bristol Myers Squibb