Associate, QC Analytical Molecular B2 Shift, Cell Therapy

Bristol-Myers Squibb

United States

On-site

USD 72,000 - 93,000

Full time

5 days ago
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Benefits offered by this job

Health Coverage
Wellbeing Support
401(k) plan

Job summary

Bristol Myers Squibb in Devens, MA, seeks a QC Analyst to support in‑process, final product, and stability testing. You will assist with GMP documentation, deviations, investigations, and continuous improvement initiatives.

Your work requires strict attention to detail, thorough following of procedures, and clear communication with peers and management in a fast‑paced team environment. Shift is Wednesday to Saturday, 2:00 p.m.–12:00 a.m. ET.

Qualifications

  • Bachelor's degree in science preferred; Associate's degree with equivalent experience may be considered.
  • 0-2+ years of analytical testing or QC experience in a regulated environment.
  • Demonstrated experience with basic laboratory techniques and safety practices.
  • Prior experience in cell and molecular biology techniques (cell-based assays, flow cytometry, qPCR) is preferred.

Responsibilities

  • Perform routine testing of in-process, final product, and stability samples.
  • Review GMP documentation and perform data verification.
  • Support document revision, CAPA and deviation/investigation related tasks and/or continuous improvement efforts.
  • May train analysts on general job duties.

Skills

Procedure adherence
Analytical testing
Laboratory equipment use
Communication
Attention to detail
Teamwork

Education

Bachelor's degree in science
Associate's degree or equivalent

Tools

Flow cytometry
qPCR
Aseptic technique

Job description

At Bristol Myers Squibb, our employees often ask, \"Who are you working for?\"-a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Position Summary

Responsible for supporting QC testing for in-process, final product, and stability samples. May assist with documentation, deviations, investigations, and continuous improvement efforts.

Shift/Days/Hours

Wednesday to Saturday 2:00 p.m. to 12:00 a.m. (Eastern Time)

Key Responsibilities
  • Perform routine testing of in-process, final product, and stability samples.
  • May review GMP documentation and perform data verification.
  • Support document revision, project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
  • May train analysts on general job duties.
  • Perform other tasks as assigned.
Qualifications & Experience
Specific Knowledge, Skills, Abilities:
  • Ability to accurately and completely understand and follow procedures.
  • Apply scientific principles to analytical testing and the proper use of laboratory equipment.
  • Ability to communicate effectively with peers and management regarding task completion, roadblocks, and needs.
  • Attention to detail and demonstrated organizational skills.
  • Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.
Education/Experience/ Licenses/Certifications:
  • Bachelor's degree preferred in science. Associate's degree with equivalent combination of education and work experience may be considered. Netherlands: Bachelor's degree /HLO in (bioanalytical) science preferred. MLO level 4 with equivalent combination of work experience may be considered.
  • 0-2+ years of relevant analytical testing or QC experience or equivalent combination of education and experience, preferably in a regulated environment.
  • Demonstrated experience with basic laboratory techniques and basic laboratory safety practices.
  • Prior experience in cell and molecular biology techniques (e.g., cell-based assays, flow cytometry, qPCR, aseptic technique) is preferred.

We hire for skills and capabilities, not just credentials - if this role excites you, but doesn't perfectly match your resume, we encourage you to apply anyway.

Compensation Overview:
  • Devens - MA - US: $36.90 - $44.71per hour

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 https://careers.bms.com/life-at-bms/.

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 ar
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