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Devens - MA - US; Devens - MA
Source: Bristol Myers Squibb careers · View original posting
From Bristol Myers Squibb's posting. “We” and “our” refer to the employer.
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.
This position works the following shift schedule: PM Shift: Sunday to Wednesday 2 PM – 12 AM.
Duties/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.
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.
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
Devens - MA - US: $36.90 - $44.71per hour
 The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws.
Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.
LAYIQ is an independent job-discovery service. This listing does not imply a partnership with or endorsement by the employer. Review the original posting for current details and availability.
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