Bristol Myers Squibb
Senior Specialist, QC Analytical, Cell Therapy B2 Shift
Bristol Myers Squibb, Harvard, Massachusetts, us, 01451
Senior Specialist, QC Analytical, Cell Therapy B2 Shift
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Senior Specialist, QC Analytical, Cell Therapy B2 Shift
role at
Bristol Myers Squibb .
Position Summary Responsible for supporting QC testing for in‑process, final product, and stability samples, including data review/verification. Perform method troubleshooting, training, and transfer/validation. Execute document revisions, projects, deviations/investigations/CAPA, and continuous improvement efforts.
Shift B2: Wednesday – Saturday 2 PM – 12 AM
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/or continuous improvement efforts.
Train and mentor others on QC test methods, processes and procedures.
Perform other tasks as assigned.
Qualifications & Experience Specific Knowledge, Skills, Abilities
Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
Demonstrated technical writing skills.
High problem‑solving ability/mentality, technically adept and logical.
Ability to communicate effectively with peers, department management and cross‑functional peers about task status, roadblocks and needs.
Ability to work in a fast‑paced team environment, meet deadlines, and prioritize work.
Advanced knowledge of LIMS, ELN and laboratory data analysis systems preferred.
Education/Experience/ Licenses/ Certifications
Bachelor's degree or equivalent required, preferably in science. (Netherlands: Bachelor's degree / HLO in (bioanalytical) science required.)
4+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.
Demonstrated experience in cell and molecular biology techniques (e.g., cell‑based assays, flow cytometry, qPCR, ELISA, and aseptic technique).
Compensation Overview US - MA: $43.84 – $53.12 per hour (salary range indicated). Final compensation will be based on demonstrated experience.
Benefits
Health Coverage: Medical, pharmacy, dental and vision care.
Wellbeing Support: BMS Well-Being Account, BMS Living Life Better, Employee Assistance Programs (EAP).
Financial Well‑being and Protection: 401(k), disability, life insurance, etc.
Work‑Life Benefits
Paid Time Off: US exempt employees – flexible time off (unlimited, with manager approval), 11 paid national holidays; Phoenix, AZ, Puerto Rico & Rayzebio – 160 hours annual paid vacation for new hires, etc.
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.
Legal Statements 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.
Candidate Rights: BMS will consider qualified applicants with arrest and conviction records where applicable.
Seniority level Associate
Employment type Full‑time
Job function Quality Assurance
Industries Pharmaceutical Manufacturing
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Senior Specialist, QC Analytical, Cell Therapy B2 Shift
role at
Bristol Myers Squibb .
Position Summary Responsible for supporting QC testing for in‑process, final product, and stability samples, including data review/verification. Perform method troubleshooting, training, and transfer/validation. Execute document revisions, projects, deviations/investigations/CAPA, and continuous improvement efforts.
Shift B2: Wednesday – Saturday 2 PM – 12 AM
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/or continuous improvement efforts.
Train and mentor others on QC test methods, processes and procedures.
Perform other tasks as assigned.
Qualifications & Experience Specific Knowledge, Skills, Abilities
Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
Demonstrated technical writing skills.
High problem‑solving ability/mentality, technically adept and logical.
Ability to communicate effectively with peers, department management and cross‑functional peers about task status, roadblocks and needs.
Ability to work in a fast‑paced team environment, meet deadlines, and prioritize work.
Advanced knowledge of LIMS, ELN and laboratory data analysis systems preferred.
Education/Experience/ Licenses/ Certifications
Bachelor's degree or equivalent required, preferably in science. (Netherlands: Bachelor's degree / HLO in (bioanalytical) science required.)
4+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.
Demonstrated experience in cell and molecular biology techniques (e.g., cell‑based assays, flow cytometry, qPCR, ELISA, and aseptic technique).
Compensation Overview US - MA: $43.84 – $53.12 per hour (salary range indicated). Final compensation will be based on demonstrated experience.
Benefits
Health Coverage: Medical, pharmacy, dental and vision care.
Wellbeing Support: BMS Well-Being Account, BMS Living Life Better, Employee Assistance Programs (EAP).
Financial Well‑being and Protection: 401(k), disability, life insurance, etc.
Work‑Life Benefits
Paid Time Off: US exempt employees – flexible time off (unlimited, with manager approval), 11 paid national holidays; Phoenix, AZ, Puerto Rico & Rayzebio – 160 hours annual paid vacation for new hires, etc.
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.
Legal Statements 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.
Candidate Rights: BMS will consider qualified applicants with arrest and conviction records where applicable.
Seniority level Associate
Employment type Full‑time
Job function Quality Assurance
Industries Pharmaceutical Manufacturing
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