AdresWorking 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: careers.bms.com/working-with-us .
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 (https://www.youtube.com/watch?v=hj8_j_FNzSU&t=19s) 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
WORKING CONDITIONS
Must be able to work in a cleanroom environment that requires gowning.
Work in areas where handling human blood products (Biosafety Level 2) will be required.
Must be able to work nights, weekends, and shift structure.
This role leads one of the Manufacturing Operations team at the Multi-Product BMS CT Manufacturing Site in Leiden, NL and will directly report into the Senior Director Manufacturing Leiden Cell Therapy Manufacturing. This role is responsible for oversight and delivery of the manufacturing start-up activities, clinical and commercial GMP Manufacturing Operations, talent management/succession planning and engagement and retention strategies for Leiden CT Manufacturing Operations.
Responsible for identifying and implementing policies, procedures, and manufacturing strategies to facilitate optimal production and performance. Responsibility includes delivering on critical project milestones and managing a functional area that will have a direct impact on the growth and success of the manufacturing facility. This role ensures the safe, validated, and compliant state of processes and procedures and develops appropriate improvement strategies to keep the operational processes with compliance and license guidance.
This role is responsible, in collaboration with Manufacturing management, to manage the Manufacturing Operations long term business strategy, business continuity plan, annual department budget, business case creation/evaluation process, portfolio management and Operational Excellence Program.
Key Responsibilities
Leading one of the BMS CT Manufacturing Operations Teams, in shift, at the Leiden site to include;
Hiring, mentoring, and developing exceptional people/teams, conducting performance reviews, and identifying opportunities for career growth for Senior Managers, Managers, and Associates.
Leading a team of 5-8 direct report and 80 indirect reports.
Ensuring a culture that embraces safety in the work environment and safety of the patients through compliance with company procedures, policies, and cGMP requirements.
Championing a culture of exceptional teamwork, accountability, continuous improvement, and communication across the organization.
Provide leadership and oversight in the implementation and execution of manufacturing processes according to established procedures and production records with CGMP’s. Address priorities, meet schedule, maximize productivity, control costs, and increase efficiency.
Qualifications & Experience
10+ or more years of experience in pharmaceutical Manufacturing Operations, manufacturing science and technology, manufacturing systems, and/or quality assurance.
8+ years leadership experience including leading leaders.
Strong knowledge of GMP compliance and GMP Manufacturing Operations.
Strong communication skills - both written and verbal communication skills with the ability to translate complex projects requirements and information into plans, improvements and standards.
Background in Protein Biologics or Cell Therapy Manufacturing required.
Certified Black Belt or equivalent certification (Lean Expert).
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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
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 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/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
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.
Company: Bristol-Myers Squibb
Req Number: R1578974
Updated: 2024-03-07 02:09:15.535 UTC
Location: Oegstgeest,Netherlands
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
