Bristol Myers Squibb
Senior Specialist, QC Analytical, Cell Therapy A2 Shift
Bristol Myers Squibb, Harvard, Massachusetts, us, 01451
Senior Specialist, QC Analytical, Cell Therapy A2 Shift
Join us to support QC testing in our Cell Therapy A2 shift at Bristol Myers Squibb.
You will perform routine test transfer, method validation, data review, and document management for in‑process, final product, and stability samples.
Position Summary Responsible for supporting QC testing for in‑process, final product and stability samples, including data review and verification. Execute method troubleshooting, training, transfer/validation and document revisions. Manage deviations, investigations, CAPA and continuous improvement initiatives.
Key Responsibilities
Perform method transfer/validation and routine testing of in‑process, final product, and stability samples.
Anticipate and perform routine troubleshooting and problem solving with minimal guidance.
Perform data verification, data review, and review of GMP documentation for general and complex methods.
Perform document revision, project, CAPA, and deviation/investigation related tasks and continuous improvement efforts.
Train and mentor others on QC test methods, processes, and procedures.
Perform other tasks as assigned.
Qualifications & Experience
Ability to accurately understand, follow, interpret and apply Global Regulatory and cGMP requirements.
Demonstrated technical writing skills.
High problem‑solving ability and logical technical aptitude.
Effective communication with peers, management, and cross‑functional teams about task status and roadblocks.
Strong teamwork, deadline management, and work‑prioritization skills.
Advanced knowledge of LIMS, ELN, and laboratory data analysis systems preferred.
Bachelor’s degree or equivalent in science (bioanalytical, chemistry, biology, or related field).
4+ years of relevant analytical testing or QC experience in a regulated environment.
Experience in cell and molecular biology techniques (e.g., cell‑based assays, flow cytometry, qPCR, ELISA, aseptic technique).
Location and Shift Shift A2: Sunday – Wednesday 2 PM – 12 AM.
Work site is at Bristol Myers Squibb manufacturing facility.
Compensation Overview US $43.84 – $53.12 per hour.
Additional incentive cash and stock opportunities may be available based on eligibility.
Benefits
Health coverage: medical, pharmacy, dental, and vision care.
Well‑being support programs and employee assistance programs.
401(k) plan, short‑ and long‑term disability, life insurance, and other financial protection.
Paid time off: unlimited paid sick time and up to 2 paid volunteer days per year.
Paid national holidays and optional holidays are available.
Equal Employment Opportunity Bristol Myers Squibb is an equal‑employment opportunity employer.
View our EEO statement at careers.bms.com/eeo.
#J-18808-Ljbffr
You will perform routine test transfer, method validation, data review, and document management for in‑process, final product, and stability samples.
Position Summary Responsible for supporting QC testing for in‑process, final product and stability samples, including data review and verification. Execute method troubleshooting, training, transfer/validation and document revisions. Manage deviations, investigations, CAPA and continuous improvement initiatives.
Key Responsibilities
Perform method transfer/validation and routine testing of in‑process, final product, and stability samples.
Anticipate and perform routine troubleshooting and problem solving with minimal guidance.
Perform data verification, data review, and review of GMP documentation for general and complex methods.
Perform document revision, project, CAPA, and deviation/investigation related tasks and continuous improvement efforts.
Train and mentor others on QC test methods, processes, and procedures.
Perform other tasks as assigned.
Qualifications & Experience
Ability to accurately understand, follow, interpret and apply Global Regulatory and cGMP requirements.
Demonstrated technical writing skills.
High problem‑solving ability and logical technical aptitude.
Effective communication with peers, management, and cross‑functional teams about task status and roadblocks.
Strong teamwork, deadline management, and work‑prioritization skills.
Advanced knowledge of LIMS, ELN, and laboratory data analysis systems preferred.
Bachelor’s degree or equivalent in science (bioanalytical, chemistry, biology, or related field).
4+ years of relevant analytical testing or QC experience in a regulated environment.
Experience in cell and molecular biology techniques (e.g., cell‑based assays, flow cytometry, qPCR, ELISA, aseptic technique).
Location and Shift Shift A2: Sunday – Wednesday 2 PM – 12 AM.
Work site is at Bristol Myers Squibb manufacturing facility.
Compensation Overview US $43.84 – $53.12 per hour.
Additional incentive cash and stock opportunities may be available based on eligibility.
Benefits
Health coverage: medical, pharmacy, dental, and vision care.
Well‑being support programs and employee assistance programs.
401(k) plan, short‑ and long‑term disability, life insurance, and other financial protection.
Paid time off: unlimited paid sick time and up to 2 paid volunteer days per year.
Paid national holidays and optional holidays are available.
Equal Employment Opportunity Bristol Myers Squibb is an equal‑employment opportunity employer.
View our EEO statement at careers.bms.com/eeo.
#J-18808-Ljbffr