Bristol Myers Squibb · 11 hours ago
Assistant QC Scientist
Summit, NJ
Contract
Onsite
Entry Level
2+ years expBristol Myers Squibb is a global biopharmaceutical company, and they are seeking an Assistant QC Scientist to support Quality Control bioanalytical testing for critical reagents. The role involves performing testing, troubleshooting, and ensuring compliance with regulatory guidelines while working collaboratively within a team.
BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
Responsibilities
Perform testing of in-process, final product, stability samples, and method transfer
Utilize scientific principles to assist in analytical testing methods and the proper use of laboratory equipment
Anticipate and troubleshoot problems
Recommend corrective actions and participate in the development of best practices
Understanding of regulatory guidelines
Complete all work in a timely manner
Work and communicate effectively within the team to ensure timelines are met
Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner
Communicate effectively with peers, and demonstrate teamwork, with regards to results of review and corrections required
Document training per procedural and cGMP requirements
Perform assigned tasks within a CAPA, deviation, or project
Draft and review technical documents, such as SOPs and forms
Communicate effectively with management regarding task completion, roadblocks, and needs
Performs other tasks as assigned
Qualification
Required
Hands-on experience with various bioanalytical techniques including ELISA, qPCR and FACS and cell-based assays
Experience in assay transfer, technology transfer, validation from Analytical Developmental group to Quality Control group
Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements
Technical writing skills
Problem-solving ability/mentality, technically adept and logical
Ability to represent the interests of the group on cross-functional teams
Ability to set priorities of the group and manage timelines
Ability to work with management locally and globally
Ability to communicate effectively with peers, department management and cross-functional peers
Bachelors degree required, preferably in Science
2-3 years of relevant work experience, preferably in a regulated environment
An equivalent combination of education and experience may substitute
The incumbent should be able to distinguish colors and possess correctable vision to 20/20, annual eye exam is required
The incumbent must analyze numerical values on a daily basis
The incumbent will be working a laboratory setting up to six (6) hours per day
The incumbent will be working with biohazardous materials, including chemical agents, up to six (6) hours per day
Preferred
The following skills are ideal for the position: Molecular-based Assays, Flow-based Assays, Purity Assays, Sample Management, and GMP Experience
Company
Bristol Myers Squibb
At Bristol Myers Squibb, we work every day to transform patients’ lives through science.
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
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