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ATTENTION MILITARY AFFILIATED JOB SEEKERS- Our organization works with partner companies to source qualified talent for their open roles. The following position is available toVeterans 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 arent 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. Youll 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.
At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition backed by a best-in-the-industry team and long-term commitment we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself accelerate your career and give new hope to patients theres no better place than here at BMS with our Cell Therapy team.
Bristol Myers Squibb is seeking a Associate QC Microbiology Cell Therapy to join our QC Microbiology team at the Cell Therapy Facility (CTF) in Devens MA. Responsible for supporting QC testing for in-process final product stability samples and for supporting environmental and facility monitoring. May assist with documentation deviations investigations and continuous improvement efforts.
Shifts Available:
Wednesday Saturday 2pm 12am (B2 - position requires shift coverage consisting of weekdays weekends holidays and during adverse weather conditions) onsite
Responsibilities:
Perform routine testing of in-process final product and stability samples.
Perform environmental/facilities monitoring and microbiological testing.
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.
Required Experience:
IC
Full Time