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Associate Director, Quality System Innovation,…
- Bristol Myers Squibb (Devens, MA)
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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 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, Quality Assurance, GoSolo Site Deployment** will play a pivotal role in helping to design and execute the future of our organization's autologous drug product manufacturing capability. This position is responsible for quality partnership in the design and implementation of next-generation technologies which support the need to reach a wider patient population through improved cost while sustaining our commitment to excellence. This role will also own the implementation of future state Quality System processes. This person will lead projects which integrate advanced technologies and methodologies, ensuring our systems are robust, efficient, and aligned with industry best practices.
Shift Available:
Monday - Friday, Standard Working Hours, Hybrid
Responsibilities:
+ Manage Quality System Deployment: Own the deployment of Next Generation Quality System processes in collaboration with the GoSolo and HyperCell visioning teams
+ Monitor and Improve Quality Systems: Monitor and evaluate the effectiveness of next generation quality systems after deployment, implementing enhancements and corrective actions as needed.
+ Cross-Functional Collaboration: Drive collaborate with cross-functional teams, including QC, Manufacturing, regulatory, and IT as the quality partner to implement next generation technologies
+ Ensure Regulatory Compliance: Drive the adoption of industry best practices and regulatory requirements, ensuring compliance and enhancing overall quality and business performance, with a focus on technology and artificial intelligence (AI)
+ Cultivate Continuous Improvement: Emphasizes innovation and continuous improvement within the organization by leveraging existing and innovating on new technologies.
Basic Requirements:
+ Bachelor's degree, preferably in a life science field; advanced degree preferred.
+ Deep subject matter experience in Quality Systems management, typically achieved through 10+ years of experience, with a proven track record of leading initiatives and driving innovation.
+ Strong knowledge of industry standards and regulatory requirements related to quality systems.
+ Demonstrated understanding and application of Quality Risk Management and lean manufacturing principles
+ Excellent leadership, communication, and project management skills.
+ Ability to work collaboratively with cross-functional teams and influence stakeholders at all levels of the organization.
+ Demonstrated ability challenge status quo and implement disruptive solutions.
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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 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.
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 [email protected] . 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.
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/
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:** R1592182
**Updated:** 2025-05-31 02:14:01.333 UTC
**Location:** Devens-MA
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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Associate Director, Quality System Innovation, GoSolo Site Deployment
- Bristol Myers Squibb (Devens, MA)