Environmental Monitoring Sampler

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. Manufacturing Shared Services Environmental Monitoring Operations is responsible for the routine /non-routine Environmental Monitoring (EM Sampling) in GMP areas of Summit West CAR-T Manufacturing and Warehouses. EM Sampler will collect environmental monitoring samples for the controlled, non-classified areas as well as controlled non-aseptic and aseptic processing areas of manufacturing.   Shift Available: Sunday - Thursday, Onsite Night Shift, 4 a.m. – 12:00 p.m.

Responsible for performing sample analysis, printing of batch labels, and creating EM sample plans. Responsible for retrieving sample plates, sanitization of EM equipment and documentation in logbooks. Responsible for collection of samples per sample plan. Responsible for delivery of samples to QC Microbiology.  Responsible for working in compliance with established safe work practices and procedures; properly uses personal protection and safety equipment as required by Bristol Myers Squibb (BMS) Reports any injury or illness immediately and notifies BMS of any hazards, unsafe acts or conditions in the workplace Performs routine processes following written instructions (SOP’s) in support of the production of pharmaceutical products with adherence to FDA or cGMP guidance. Work in an aseptic production environment. Must be able to wear appropriate clean room attire (i.e. surgical masks, sterile gown) and all Personal Protective Equipment (PPE). Responsible for accurate completion of all EM Sampling documentation. Operate and maintain equipment and work area to ensure cleanliness and safety following GMPs and SOPs. Ensure that materials and equipment in the Manufacturing area are maintained in accordance with GMPs and SOPs. Contribute to achieving continuous improvement. Must work independently with minimal supervision. Must successfully complete training on aseptic gowning procedures and demonstrate the ability to aseptically gown. Ensure compliance with current Good Manufacturing Procedures (cGMP), USP, EU, and other global regulatory requirements at all times. Follow directions properly and work cooperatively as an individual contributor and as a team member. Communicate effectively with Manufacturing Operations peers, cross-functional peers, and management. Assist in troubleshooting and solving problems that may come up in the day-to-day operation of the department. Perform Environmental Monitoring on a routine and non-routine basis for all S12, S6A & S16 GMP manufacturing and associated warehouse areas. Assist with investigations & CAPAs associated with EM excursions. Perform all other duties as assigned. Flexibility with the schedule (weekends, holidays, extended hours, and rotating/staggered shifts) is an absolute must. Knowledge & Skills: Experience with cold chain sample storage and transfer. Knowledge of cGMP/FDA regulated industry. Basic mathematical skills. General understanding of cGMPs. Technical writing capability. Proficient in MS Office