Bristol Myers Squibb · 1 day ago
Manager Quality Assurance Disposition Support
Devens, MA
Full-time
Onsite
Mid Level
$100K/yr - $122K/yr
4+ years expBristol Myers Squibb is a company dedicated to transforming patients' lives through science. The Manager, Quality Assurance Disposition Support role involves overseeing the Quality Disposition organization and supporting various functions including incoming materials QA and disposition, while interfacing with multiple departments to ensure compliance and quality standards.
BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
Responsibilities
Owning and driving Quality System records
Performing product and change impact assessments
Support the systems and data requests needed
Maintain QD monitoring tools and metrics
May represent the QD program in audits and inspections
Performing routine Drug Product and Incoming Material disposition, as required, during peak and overflow periods
Maintain inspection plans and SAP infrastructure for disposition operations
Perform testing for eSystem changes as needed
Other tasks as required by Quality Disposition leadership
Monitoring quality events and impact assessments, as needed, for potentially non conforming lots
Sending Pre-MRB Notification to Mgt and MRB stakeholders along with scheduling MRB meetings and deliverables
Collaborating with SMEs to obtain inputs and investigative information for MRB decision-making
Attending MRB meetings and assisting in determination, with MRB, available treatment options for patients
Managing confidential MRB documentation appropriately
Qualification
Required
Bachelor's degree in STEM field preferred. High school diploma/ Associates degree with equivalent combination of education and work experience may be considered
4-5 years of experience in a regulated industry with 1+ year quality experience. Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred
Demonstrated experience with electronic system and databases
Ability to research, understand, intepret and apply internal policies and regulatory guidelines
Proficient computer skills with knowledge of several digital tools like MS Office, Smartsheets etc. and ability to learn and work with new software applications
Ability to interpret data & results, understand complex problems with multiple variables and critically assess and provide feedback on proposed solution and required documentation
Ability to critically review investigation reports, interpret results and assess and challenge technical conclusions consistent with Quality risk management principles
Excellent verbal and technical writing skills with ability to prepare written communications and present technical data to management with clarity and accuracy
Ability to work in a fast-paced team environment and changing priorities
Detail oriented and task focused with ability to meet deadlines and prioritize work
Ability to think strategically , meet deadlines and prioritize work
Able to work across functional groups and teams to ensure requirements are met
Self motivated and contribute to a positive team environment
Confident in making decisions for medium level issues and able to recognize Quality issues and solve problems
Curious and ability to think critically to create innovative solutions
Preferred
Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred
Benefits
Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Paid Time Off
US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work.
Company
Bristol Myers Squibb
At Bristol Myers Squibb, we work every day to transform patients’ lives through science.
10001+ employees
H1B Sponsorship
Bristol Myers Squibb has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (247)
2024 (278)
2023 (231)
2022 (180)
2021 (181)
2020 (169)
Funding
Current Stage
Public CompanyTotal Funding
$29.32BKey Investors
Venrock
2025-11-05Post Ipo Debt· $5.74B
2024-02-14Post Ipo Debt· $13B
2023-10-30Post Ipo Debt· $4.5B
Leadership Team
Charles Bancroft
CFO
Cristian Massacesi
Executive Vice President, Chief Medical Officer and Head of Development
Recent News
2026-01-07
2026-01-07
2026-01-07
Company data provided by crunchbase