Clinical Manufacturing Associate II, Cell Therapy in Devens, MA

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.

Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.

We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.

This is work that transforms the lives of patients, and the careers of those who do it.

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, there’s no better place than here at BMS with our Cell Therapy team.

The Clinical Manufacturing Associate II, Cell Therapy brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs.

The Associate must be goal-oriented, flexible, and able to work efficiently with safety and quality in mind.

The Associate must be enthusiastic, and innovative individuals with a good understanding of good manufacturing practices to support Clinical Manufacturing Start Up activities, and direct manufacturing operations for Clinical Cell Therapy.

Shifts Available:

TBD

Responsibilities:


* Performing Clinical patient process unit operations and supporting operations described in standard operating procedures and batch records.


* Demonstrates strong practical and theoretical knowledge of work


* Completing documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records.


* Solving simple problems; taking new perspectives using existing solutions


* Identifies innovative solutions


* Performing tasks in a manner consistent with the safety policies, quality systems, and cGMP requirements.


* Completing training assignments to ensure the necessary technical skills and knowledge.


* Referencing Batch Records, Standard Operating Procedures and Work Instructions to successfully complete manufacturing operations.


* Executing daily unit operations schedule that includes people, product, and material flow across multiple shifts.


* Working in a cleanroom environment and performing aseptic processing; maintaining manufacturing environmental conditions (Non-Viable Particulate(s) and Viable microbial levels per controlled area classification specifications) by performing area disinfection regiment as required to meet global Health Authority requirements.


* Collaborating with support groups on recommendations and solving technical and operational problems.


* Assisting in setting up manufacturing areas ...