QC STAT Associate - Devens, MA

, ATTENTION MILITARY AFFILIATED JOB SEEKERS, - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to, Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is 'On-Site' at the location detailed in the job post.Challenging. Meaningful. Life-changing. Those arenât words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. Youâll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.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., Position: QC STAT AssociateLocation: Devens, MA, Night shift (5pm-5am rotational A2 and B2 schedules) therefore elegible for a 20% shift differential, Key Responsibilities:Perform routine testing and data review of in-process and batch release samples of Bulk Drug Substance in a cGMP compliant environment.Perform 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).Perform activities to support lab operations such as housekeeping, alarm acknowledgement, reagent preparation, inventory management, material and reagent ordering, sample pickup and discarding, and execution of work orders.Ability to understand and follow procedures while working in a fast-paced team environment, meet deadlines, and adjust to changing priorities.May write and revise QC documents for managerial review and approval.May train colleagues on basic and some more complex test methods.Supports deviation investigations and laboratory investigations through data gathering or interview process. , May lead no impact deviations and Lab Investigations.Identifies and escalates challenges ,barriers to execution, suggests solutions, and participates in remediation while assisting with a broad range of troubleshooting activities.Actively and positively learns and participates in Operational Excellence (OpEx) and Continuous Improvement (CI) initiatives in the team.Positive, supportive, and actively collaborates within the team and other sub-teams within QC or cross-functionally outside of plete all required tasks compliantly and safely while consistently and intentionally modeling BMS values (Integrity, Accountability, Passion, Urgency, Innovation, and Inclusion).Ability to understand and follow procedures while working in a fast-paced team environment, meet deadlines, and adjust to changing priorities. , , , , ,

Created: 2025-11-01