QC STAT Associate

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Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

Bristol-Myers Squibb is seeking a quality control professional to join our QC STAT team, performing QC testing in support of biologics bulk drug substance manufacturing using defined methods in a cGMP compliant laboratory. The QC Associate assures test results are accurately recorded and abnormal data or equipment/instrument malfunctions are promptly reported to his/her supervisor.

The QC STAT AM team works a 12-hour shift (5AM to 5PM) with rotating work days across a 2-week period (36/48).

Qualifications:

·       Knowledge of science generally attained through studies resulting in a BS degree, preferably in Chemistry, Molecular Biology, or related discipline.

·       A minimum of 0-2 years of experience in a Biologics QC laboratory or related biopharmaceutical cGLP or cGMP lab.

·       Experience in analytical test methods such as UV/Vis, HPLC, TOC, and protein purification highly preferred.

·       Knowledge of lab software applications (e.g., LIMS, ELN (LES/SmartLab), Empower) preferred.

·       Excellent manual dexterity including proficiency in aseptic techniques desired.

·       High attention to detail with strong general laboratory and good organizational skills.

·       Demonstrated ability to work independently as well as part of a team, to complete assignments within defined time constraints.

·       Ability to interpret and apply cGMPs, USP, regulatory requirements and industry best practices.

·       Demonstrates problem solving and analytical thinking skills.

Responsibilities:

·         Performs routine testing and data review of in-process and batch release samples of Bulk Drug Substance in a cGMP compliant environment.

·         Performs routine assays such as UV-VIS Spectrometry, Titer, utility testing, personnel and environmental monitoring, Total Organic Carbon testing, and more complex assays including various HPLC methodologies (e.g., sialic acid).

·         Performs broad range of troubleshooting techniques and leads such within area of expertise.

·         May write and revise SOPs for managerial review and approval.

·         May train less experienced analysts on basic and some more complex test methods.

Work Environment:

·         QC Associates will work in teams and have continual interaction with members of his/her team as well as other teams throughout the facility to exchange information regarding testing completed, in process and planned. 

·         All QC Associates will have daily contact with her/his supervisory staff for work assignments, coaching and general management discussions. Incumbents normally receive general instructions on routine work and specific instructions on new assignments.

·         Occasional contact with other line management staff relating to specific project responsibilities may be expected.

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If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-