Manufacturing Associate II

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.

Position Summary 

Our Associates perform a crucial role in driving our novel cell therapy programs by supporting routine manufacturing operations.

We are searching for innovative, intellectually curious individuals with a general understanding of Good Manufacturing Practices (GMPs) to support routine manufacturing operations for Cell Therapy.

Successful candidates must be goal-oriented and flexible, with the ability to work effectively and efficiently on a team while demonstrating safety, quality, and GMP compliance at all times.  

BMS Values  

• Our values move us toward our mission to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.  

• Candidates must exemplify the BMS values of Passion, Integrity, Inclusion, Accountability, Innovation, and Urgency.

 

Duties/Responsibilities  



* Learn and execute Cell Therapy Manufacturing operations compliantly  



* Execute operations as outlined in Source Governing Documents (including but not limited to: Standard Operating Procedures, Work Instructions, Batch Records, Forms)  



* Demonstrate strong practical and theoretical knowledge  



* Executes transactions and process in all electronic systems and adheres to business continuity processes  



* Prioritizes safety of self and others  



* Reports safety events within 24 hours  



* Immediately escalates any/all issues that may impact compliance or safety of self and/or others.  



* Complete documentation required by Source Governing Documents contemporaneously  



* Perform all tasks in a manner consistent with the safety policies, SOPs, quality systems, and GMP requirements including ALCOA+  



* Complete training assignments prior to assigned due date to ensure the necessary technical skills and knowledge  



* Trains for proficiency in process systems and some supporting business systems, and maintains trainer qualifications  



* Collaborate with support groups on recommendations and solving technical and operational problems  



* Train others on Source Governing Documents to successfully complete manufacturing operations  



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



* Work within a controlled cleanroom environment and execute asepti...