Bioprocess Associate

Working with UsChallenging. Meaningful. Life-changing. Those aren’t 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. You’ll 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. Read more: careers.bms.com/working-with-us.Position: Bio Process Associate DownstreamLocation: Devens, MA facility Rotating Shift: A Days (12 hour rotational, 5:00PM to 5:00AM) therefore elegible for a 20% shift Differential.Key ResponsibilitiesWorks on routine manufacturing assignments per written procedures that are complex with on instructions, where ability to recognize deviation from accepted practice is required.Adheres to Good Manufacturing Practices and standard operating procedures. Weighs and checks raw materials.Assembles, cleans and sterilizes process equipment, monitors processes.Completes electronic work instructions and maintains clean room environment to comply with regulatory requirements.Operates all production equipment within the assigned functional area (i.e. Upstream: Media formulation equipment, glass washers, dispensary, bioreactors, harvest equipment or Downstream: Buffer equipment, glass washers, chromatography skids, membrane operations, column packing skids, etc.).Effectively uses process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP, Trackwise, Maximo etc.). Ensures less experienced manufacturing personnel comply with Standard Operating Procedures (SOPs) and electronic work instructions.Assists with the coordination and implementation of special projects such as validation or complex investigations.Revises and creates process documents with no instructions, supports routine process investigations.Assists with reviewing batch and exception reports for each manufacturing lot in conjunction with Quality representative.Champions areas specific initiatives associated with work safety.Engages in and supports culture of continual improvement through ownership of improvement for work processes, equipment and safe work environment.Qualifications & Experience • High school diploma is required; knowledge of science generally attained through studies resulting in a B.S. in science, engineering, biochemistry or related discipline is desired but not required.• A minimum of 5+ years process operations experience in a highly automated biotechnology manufacturing facility subject to Good Manufacturing Practices (GMP) regulations.• Strong knowledge of either upstream and/or downstream unit operation is essential.• Practical knowledge of regulations such as GMP and company Standard Operating Procedures (SOP).• Prior evidence of successful participation on work teams where combined contribution, collaboration, and results were expected.• Demonstrated proficiency in common computer tools such as word processing, spreadsheet and web-based applications.• Previous work experience where attention to detail and personal accountability were critical to success.• Demonstrates good interpersonal skills, is attentive and approachable.If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Compensation Overview:Devens - MA - US: $25.34 - $30.70per hour The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/. Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:Health Coverage: Medical, pharmacy, dental, and vision care.Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.​Work-life benefits include:Paid Time OffUS Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidaysBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.All global employees full a