Bristol Myers Squibb Associate Director, Material Review Board Process Owner, Cell Therapy in Devens, Massachusetts
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: careers.bms.com/working-with-us .
At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.
The Associate Director, Material Review Board Process Owner is part of the BMS Cell Therapy Quality Systems organization. At the intersection of people, process, and systems is the Business Process Owner (BPO) network. The BPO for Material Review Board works with an expanding network of internal and external stakeholders to foster cross-site collaboration, harmonize business process and deliver a road map for continuous improvement, systems implementation and help drive decision-making for initiatives associated with Quality inputs/processes related to Material Review Board (MRB) and the Out of Specification (OOS) release process.
The MRB Process Owner is positioned within the Disposition Business Process Owner team. This team is responsible for ensuring that all disposition related processes within Cell Therapy are executing compliantly, efficiently, and in a standardized fashion across the network. While this specific role is focused within the out of specification release workflow, including MRB, initiatives and projects supporting the overall disposition program are also in scope. This is an individual contributor position reporting directly to the Director, Cell Therapy Quality Disposition Process Owner.
The MRB Process Owner works closely with Cell Therapy subject matter experts, legal, regulatory, medical affairs, and IT partners. This is an exciting opportunity to shape how BMS’s Cell Therapy manufacturing network operates and be part of a team influencing the overall future of the Cell Therapy network.
Serve as the CTDO Process Owner for MRB
Lead the MRB Community of Practice
Partner with franchise on internal and external communications associated with the MRB process
Support development of Out of Specification Release Processes for new sites, markets and/or indications within the CTDO network
Develop the strategy and business process road map for Cell Therapy MRB
Lead, develop and implement policies and procedures based on current regulations and industry standards to ensure readiness for scalability within Cell Therapy
Partner with cross-functional leaders to ensure compliant and scalable processes.
Work with senior leaders to help establish performance goals and strategic/operational objectives for MRB and OOS workflows.
Develop process metrics that can be used to provide performance insights to stakeholders
Qualifications & Experience:
Bachelor's degree in a life sciences or engineering discipline and a minimum of 7+ years of relevant biotechnology or pharmaceutical industry experience including direct experience with Quality Systems.
Cell Therapy experience is strongly preferred.
Experience participating in cross-functional matrix teams.
Excellent oral and written communication skills. Skilled at presenting complex topics to senior leaders.
Proven record leading or contributing to projects or programs in support of GXP operations
Experience with regulatory inspections
Extensive knowledge of current industry practices
Experience with interpretation and application of guidelines and regulations
Proven ability to adjust to multiple demands, shifting priorities and unexpected events while maintaining a positive work attitude
The starting compensation for this job in Seattle, WA is a range from $149,000-$188,000, plus incentive cash and stock opportunities (based on eligibility).
The starting pay rate takes into account characteristics of the job, such as required skills and the where the job is performed.
Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit our BMS Careers site: https://careers.bms.com
Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.
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.
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 firstname.lastname@example.org . 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: R1578089
Updated: 2024-02-23 01:42:03.667 UTC
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.
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