Manufacturing Associate II

Job description

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 aseptic processing procedures (as assigned). Maintain 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 Continues to refine and improve manufacturing process technique to improve individual operational times. Verifies training completion prior to performing any GxP tasks Reporting Relationship Reports to Manager, Manufacturing Operations Qualifications Education: U.S. • Associate or bachelor's degree in related field is preferred • A minimum high school diploma and/or equivalent combination of education and experience is required Netherlands • MBO, 3 of 4 in science related field and/or equivalent Experience: • 1+ years of cGMP cell therapy manufacturing, bioprocessing manufacturing, or relevant experience and education • Proven experience working on teams where combined contribution, collaboration, and results were expected • Proficiency in common computer tools such as word processing, spreadsheet and web-based applications • Meticulous attention to detail and personal accountability are critical to success • Demonstrated good interpersonal skills, is attentive and approachable • Maintain a professional and productive relationship with area management and co-workers • Basic understanding of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing is required Preferred Experience: • Experience in cell therapy manufacturing, including Cell washing, Cell Expansion processes and automated equipment. Cell separation techniques and automated equipment. Cryopreservation processes and equipment. Working Conditions: • Must be able to stand/walk for extended periods of time • Must be able to work in a cleanroom environment and perform aseptic processing in ISO 5 biosafety cabinets (as assigned), which require gowning and personal protective equipment (PPE), including by not limited to: safety shoes, safety glasses, aprons, face shields, powered air purifying respirators (PAPR), lab coats, full body gowns, hairnets, gloves, and hearing protection. • Required to carry and/or lift up to 30 pounds / 15 kg, several times a day, while handling production equipment and/or materials • Required to push and/or pull up to 50 pounds / 25 kg, several times a day, while handling production equipment and/or materials • Work in areas that may have strong magnets • Must be able to work in a BSL2 / ML1 work environment handling human blood components Work in areas with exposure to vapor phase liquid nitrogen • Must be able to work assigned shift (Day, Evening, Night, Weekends and/or Holidays) This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job. This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management. Shifts available: Days – Sun – Tue (alt. Wed) 0500 – 1730 Days – Thu – Sat (alt. Wed) 0500 – 1730 Swing – Sun – Tue (alt. Wed) 1100 – 2330 Swing – Thu – Sat (alt. Wed) 1100 - 2330 BMSCART #LI-ONSITE We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway. Compensation Overview: Bothell - WA - US: $33.67 - $40.80per hour The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance. Benefits: Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans – including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability). U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year. Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid compan