Bristol Myers Squibb · 1 day ago
Quality - Sample Management
Devens, MA
Contract
Onsite
New Grad, Entry Level
$22/hr - $24.47/hrBristol Myers Squibb is a global biopharmaceutical company committed to discovering, developing, and delivering innovative medicines. The Quality - Sample Management role involves routine processing and data review of samples in a cGMP compliant environment, inventory management, and executing procedures within the Sample Management functional area.
BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
Responsibilities
Performs routine processing and data review of raw materials, in-process, batch release, and/or stability samples of Bulk Drug Substance in a cGMP compliant environment
Performs routine inventory and sample management of routine samples, critical reagents and non-routine samples. Main responsibilities include Chain of Custody
Executes routine procedures owned by the Sample Management functional area. Assignments are made in the LMS, by the hiring manager, based on applicable curricula map(s)
Knowledge of science generally attained through studies resulting in a AS or certificate program in the physical or life sciences, supply chain, a related discipline, or the equivalent in related experience
Knowledge of basic laboratory techniques such as working in a BSC, pipetting, aseptic technique; basic laboratory safety practices preferred
Familiarity with controlled temperature storage, sample inventory, and sample shipment and receipt
Attention to detail and demonstrated organizational skills
Demonstrated manual dexterity
Will work in teams and have continual interaction with members of his/her team as well as other sub-teams within Quality Control Organization, in order to exchange information regarding sample management as it relates to meeting department goals and objectives
Daily contact with her/his supervisory staff for work assignments. Routine contact with supervisor for coaching and general performance management discussions
Occasional contact with other line management staff relating to specific project responsibilities may be expected
Occasional contact with Manufacturing and Stability organizations for escalation where appropriate
Occasional contact with other sites/vendors for tactical logistical purposes
Associates primarily work in a cGMP laboratory and follow techniques which require one to be alert, giving ahigh attention to detail, to properly use Personal Protective Equipment (PPE)and to handle hazardous materials
Associates should be observant of their work area and related tools and identify and report any discrepancy from normal practice or procedure
Knowledge of basic electronic systems (email, MS Office, etc.)
Attention to detail is key
Qualification
Required
Performs routine processing and data review of raw materials, in-process, batch release, and/or stability samples of Bulk Drug Substance in a cGMP compliant environment
Performs routine inventory and sample management of routine samples, critical reagents and non-routine samples. Main responsibilities include Chain of Custody
Executes routine procedures owned by the Sample Management functional area. Assignments are made in the LMS, by the hiring manager, based on applicable curricula map(s)
Knowledge of science generally attained through studies resulting in a AS or certificate program in the physical or life sciences, supply chain, a related discipline, or the equivalent in related experience
Attention to detail and demonstrated organizational skills
Demonstrated manual dexterity
Will work in teams and have continual interaction with members of his/her team as well as other sub-teams within Quality Control Organization, in order to exchange information regarding sample management as it relates to meeting department goals and objectives
Daily contact with her/his supervisory staff for work assignments. Routine contact with supervisor for coaching and general performance management discussions
Occasional contact with other line management staff relating to specific project responsibilities may be expected
Occasional contact with Manufacturing and Stability organizations for escalation where appropriate
Occasional contact with other sites/vendors for tactical logistical purposes
Associates primarily work in a cGMP laboratory and follow techniques which require one to be alert, giving a high attention to detail, to properly use Personal Protective Equipment (PPE) and to handle hazardous materials
Associates should be observant of their work area and related tools and identify and report any discrepancy from normal practice or procedure
Knowledge of basic electronic systems (email, MS Office, etc.)
Attention to detail is key
HS Diploma required OR enrolled in a scientific program
Preferred
Knowledge of basic laboratory techniques such as working in a BSC, pipetting, aseptic technique; basic laboratory safety practices preferred
Familiarity with controlled temperature storage, sample inventory, and sample shipment and receipt
Company
Bristol Myers Squibb
At Bristol Myers Squibb, we work every day to transform patients’ lives through science.
Founded in 1887
10001+ employees
H1B Sponsorship
Bristol Myers Squibb has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (247)
2024 (278)
2023 (231)
2022 (180)
2021 (181)
2020 (169)
Funding
Current Stage
Public CompanyTotal Funding
$29.32BKey Investors
Venrock
2025-11-05Post Ipo Debt· $5.74B
2024-02-14Post Ipo Debt· $13B
2023-10-30Post Ipo Debt· $4.5B
Leadership Team
Charles Bancroft
CFO
Cristian Massacesi
Executive Vice President, Chief Medical Officer and Head of Development
Recent News
2026-01-07
2026-01-07
2026-01-07
Company data provided by crunchbase