Senior Specialist, Quality Assurance Investigations, Cell Therapy
$89.78k - $108.79kBristol-Myers Squibb
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 .
Position: Senior Specialist, Quality Assurance Investigations, Cell Therapy
Location : Devens, MA
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
Position Summary
The Senior Specialist, Quality Assurance Investigations, is responsible for quality oversight and approval of Deviation investigations and associated Action and Effectiveness Check records at the Devens Cell Therapy Facility. The role provides Quality oversight and assurance of the quality of manufactured products, in compliance with all applicable regulations and BMS policies and guidelines.
Key Responsibilities
Review and approve investigations/ CAPAs / effectiveness checks associated with the manufacturing site including but not limited to materials, manufacturing, laboratory, facility, and computer systems.
May author, review, approve technical reports, including but not limited to risk assessments and deviation system monitoring reports, to support the deviations program.
Ensure the corrective/ preventive actions are robust and adequately address the root cause
May perform routine reporting and analysis of metrics to ensure timely closure of quality events and actions.
Identifies improvement opportunities and supports execution of site/team continuous improvement goals and projects.
Support internal and external inspections as required.
Maintain compliance with assigned learning plan. Support development and delivery of training content to cross functional teams.
Lead meetings and represent function at cross functional meetings. Share data/ knowledge within and across team. Build & maintain strong relationships with partner functions.
Qualifications & Experience
Specific Knowledge, Skills, Abilities:
Ability to research, understand, interpret and apply internal policies and regulatory guidelines.
Proficient computer skills with knowledge of several digital tools like MS Office, Smartsheet, etc. and ability to learn and work with new software applications.
Ability to interpret data & results, understand problems with few variables and critically assess and provide feedback on proposed CAPA.
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 support work prioritization.
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 minor issues and able to recognize Quality issues and solve problems.
Curious and ability to think critically to create innovative solutions.
Education/Experience/ Licenses/Certifications:
Bachelor's degree in STEM field preferred. High school diploma/ Associate's degree with equivalent combination of education and work experience may be considered.
4+ years of experience in a regulated industry with 1+ year deviation experience. Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred.
Demonstrated experience with electronic system and databases
Demonstrated experience in root cause analysis tools including but not limited to 5-WHY, Human error prevention, Ishikawa Diagram (Fishbone Analysis), Process Flow Diagram, etc.
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 View email address on click.appcast.io . Visit careers.bms.com/ ( 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.
#LI-ONSITE
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.
Compensation Overview:
Devens - MA - US: $89,780 - $108,789
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. 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
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
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.
Work-life benefits include:
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
Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
*Eligibility Disclosure: T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
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 View email address on click.appcast.io . Visit careers.bms.com/ ( eeo-accessibility 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.
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:
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at .
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at View email address on click.appcast.io . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
R1602076 : Senior Specialist, Quality Assurance Investigations, Cell Therapy Company: BMS
Req Number: R1602076
Updated: 2026-06-14 04:49:59.493 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.
$89.78k - $108.79k
...to the latest breakthroughs in cell therapy, this is work that transforms... ...com/working-with-us . The Senior Specialist, QA Investigations , is responsible for quality oversight and approval of Deviation... ...Quality oversight and assurance of the quality of manufactured...SeniorHourly payFull timeTemporary workPart timeFor contractorsWork experience placementSummer workLive inLocal areaRemote workFlexible hoursShift work- Position Summary The Senior Specialist, Quality Assurance Investigations, is responsible for quality oversight and approval of Deviation investigations and... ...and Effectiveness Check records at the Devens Cell Therapy Facility. The role provides Quality oversight and assurance...SeniorFull timeWork experience placement
$89.78k - $108.79k
Senior Specialist, QA Investigations The Senior Specialist, QA Investigations, is responsible for quality oversight and approval of Deviation investigations... ...records at the Devens Cell Therapy Facility. The role... ...Quality oversight and assurance of the quality of manufactured...SeniorFull timeTemporary workWork experience placementFlexible hours$89.78k - $108.79k
Position Summary The Quality Assurance Shop Floor team is responsible... ...cGMP. As a QA Shop Floor Senior Specialist, you will serve as a... ...complaints, deviations, investigations and CAPA management. Demonstrated... ...in biopharmaceuticals or cell therapy manufacturing is...SeniorFull timeTemporary workWork experience placementSummer workFlexible hoursDay shift$89.78k - $108.79k
Bristol Myers Squibb is seeking a Senior Specialist for Quality Assurance Investigations at the Devens Cell Therapy Facility. This role oversees Deviations and ensures compliance with all regulations and internal policies. The ideal candidate will hold a Bachelor’s degree...Senior- ...procedures, and Global cGMP. Provides 24x7 Quality collaboration and oversight of site... ...Reports to the Shift Manager, Quality Assurance Shop Floor. Rotating 2-3-2 Panama schedule... ...regulations in biopharmaceuticals or cell therapy manufacturing preferred. Demonstrated experience...SeniorTemporary workWork experience placementShift workDay shift
$43.84 - $53.12 per hour
Senior Specialist, QC Analytical, Cell Therapy Location: Devens, MA. Shift: B2 (2pm-12am, Wednesday‑Saturday). Compensation: $43.84-$53.12 per hour. Additional... .... Execute document revisions, projects, deviations/investigations/CAPA, and continuous improvement efforts. Duties /...SeniorHourly payTemporary workSummer workFlexible hoursShift work$43.84 - $53.12 per hour
Senior Specialist, QC Analytical, Cell Therapy A2 Shift Position Summary Responsible for supporting QC testing for in-process, final product, and stability... .... Execute document revisions, projects, deviations/investigations/CAPA, and continuous improvement efforts. Shift A2:...SeniorHourly payFull timeTemporary workSummer workFlexible hoursShift work$43.84 - $53.12 per hour
.... Execute document revisions, projects, deviations/investigations/CAPA, and continuous improvement efforts. Duties/Responsibilities... ...should be directed to Chat with Ripley. R1601149 : Senior Specialist, QC Microbiology, Cell Therapy Company: Bristol-Myers Squibb Req Number: R1601149...SeniorHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$89.53k - $108.49k
...latest breakthroughs in cell therapy, this is work that... ...to maintaining quality oversight and ensuring... ...manufacturing operations. The Senior Field QA Specialist is responsible for... ...Operations to investigate and resolve... ...to real-time quality assurance, batch release readiness...SeniorHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workMonday to FridayFlexible hoursShift workAfternoon shift- Bristol Myers Squibb in Massachusetts is looking for a Senior Specialist, QC Analytical, to support testing of in-process and final products, tackling method validation, troubleshooting, and mentoring others. The role requires a Bachelor’s degree and 4+ years of relevant...SeniorFlexible hoursAfternoon shift
- ...Bristol Myers Squibb is seeking a Senior Specialist, QA Investigations, responsible for quality oversight of Deviation investigations at the Devens Cell Therapy Facility. The role ensures compliance with quality regulations and BMS guidelines. The ideal candidate has...Senior
- Scorpion Therapeutics is seeking a Quality Assurance professional in Harvard, Massachusetts to oversee compliance with quality standards in manufacturing and operations. The role involves ensuring compliance, documentation verification, and quality oversight in fast-paced...Senior
$33.51 - $40.61 per hour
...tasks consistent with safety policies, quality systems, and GMP requirements. Complete... ...support manufacturing operations. Support investigations. Identify innovative solutions. Assist... ...guidance applicable to biologics and cell therapy manufacturing. Ability to work assigned...SeniorHourly payFull timeShift workNight shiftRotating shift$40.05 - $48.53 per hour
...latest breakthroughs in cell therapy, this is work that... ...Therapy team. The Specialist, Lead Clinical... ...novel programs. The Senior Associate must be goal... ...efficiently with safety and quality in mind. The Senior... ...Supporting quality event investigations Any related tasks...Hourly payFull timeTemporary workPart timeFor contractorsWork experience placementSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift workNight shiftWeekend work$33.51 per hour
...professional in Massachusetts who is skilled in cGMP bioprocessing and cell therapy manufacturing. The role involves executing and documenting... ...SOPs, training staff, and ensuring compliance with safety and quality systems. This position requires a high school diploma and at...SeniorHourly payFull time- Bristol Myers Squibb is hiring a Senior Manufacturing Associate in Devens, MA to support routine manufacturing operations for cell therapy products. The role requires strong knowledge of cGMP regulations and experience in cleanroom environments. The ideal candidate will...SeniorHourly payFull timeDay shift
- ...Senior Manager, Operational Excellence, Cell Therapy The Senior Manager, Operational Excellence, Cell Therapy is responsible... ...deliver best‑in‑class safety, quality, productivity and cost across... ...during production. Provide investigation support for production related investigations...SeniorTemporary workShift work
$35.82 - $43.41 per hour
...optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the... ...stability samples. May assist with documentation, deviations, investigations, and continuous improvement efforts. Duties /...Hourly payTemporary workWork experience placementSummer workRemote workFlexible hoursShift work- ...latest breakthroughs in cell therapy, this is work that transforms... .... Position Summary The Senior Manager, Quality Assurance Shop Floor (QASF) 2nd... ...operators and Field QA specialists; hire, develop, and conduct... ...complaints, deviations, investigations, and CAPA management....SeniorSummer workLive inRemote workMonday to FridayFlexible hoursShift workNight shiftRotating shiftAfternoon shift
- Bristol-Myers Squibb is seeking a QA Shop Floor Senior Specialist to ensure quality compliance across site operations in Massachusetts. Responsibilities include overseeing manufacturing processes and ensuring GxP compliance, reviewing quality records, and leading cross-...Senior
$33.51 - $40.61 per hour
...Senior Manufacturing Associate, Cell Therapy Working with us is anything but usual. Here, uniquely interesting... ...work efficiently with safety and quality in mind. We are searching for... ...manufacturing operations. Supports investigations. Identifies innovative...SeniorHourly payFull timeTemporary workPart timeSummer workWork at officeFlexible hoursShift workNight shiftRotating shiftDay shift$137.79k - $166.97k
...the latest breakthroughs in cell therapy, this is work that transforms... ...Cell Therapy team. The Senior Manager, Operational Excellence... ...best in class safety, quality, productivity and cost across... ...conduct route cause analysis investigation, design future state and develop...SeniorHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$58 - $61.01 per hour
Overview The BMS Devens Cell Therapy Manufacturing Site has been selected as the launch site of... ...project schedules, and present status to senior management and stakeholders. Lead or support completion of complex investigations, initiate change controls (assessing impact...Hourly payContract workTemporary workFor contractorsLocal areaMonday to Friday- ...responsible for supporting QC testing for in-process, final product, and stability samples as well as assisting with documentation and investigations. Ideal candidates will have a degree in science and some experience in QC or analytical testing. This position offers...Hourly payShift work
$29.83 - $36.15 per hour
...latest breakthroughs in cell therapy, this is work that... ...Bioprocess Associate/Specialist assists in the execution... ...with process related investigations. 8. Leads in... ...with supervisor and Quality representative. 10. Assists... ...1603433 : Downstream Senior Bioprocess Associate...SeniorHourly payFull timeTemporary workPart timeFor contractorsWork experience placementSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$35.82 - $43.41 per hour
...product, and stability samples and for supporting environmental and facility monitoring. May assist with documentation, deviations, investigations, and continuous improvement efforts. This position works the following shift schedule: Wednesday to Saturday 6 AM - 4 PM. Key...Hourly payFull timeTemporary workWork experience placementSummer workFlexible hoursShift work- Bristol Myers Squibb in Devens, MA is seeking a Senior Specialist, QC Analytical, to support testing for in-process, final product, and stability samples. Responsibilities include method troubleshooting, training, and data verification. The ideal candidate has at least...SeniorFlexible hours
$131.75k - $159.65k
Senior Manager, Cell Therapy Manufacturing Location: Devens, MA Responsibilities Serves as manufacturing functional area owner and manages commercial... .... Building effective cross‑functional relationships with Quality, Supply Chain, MS&T, EHS and F&E. Ensuring a culture that...SeniorHourly payFull timeTemporary workPart timeWork experience placementSummer workFlexible hoursShift work$131.75k - $159.65k
...production line to the latest breakthroughs in cell therapy, this is work that transforms the lives... ...BMS with our Cell Therapy team. The Senior Manager, Cell Therapy Manufacturing... ...cross-functional relationships with Quality, Supply Chain, MS&T, EHS and F&E. Ensuring...SeniorHourly payFull timeTemporary workPart timeFor contractorsWork experience placementSummer workLive inWork at officeLocal areaRemote workMonday to FridayFlexible hoursShift work
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