Downstream Senior Bioprocess Associate - Night Shift

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Working with Us Challenging. 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 . Summary: The Bioprocess Associate/Specialist assists in the execution of manufacturing processes according to established work instructions and production records for the manufacture of therapeutic proteins in accordance with current Good Manufacturing Practices (cGMPs) Shift: B2 rotating shift 6:00PM-6:30AM Major Duties and Responsibilities 1. Works on routine manufacturing assignments per written procedures that are moderately complex with minimal instructions, where ability to recognize deviation from accepted practice is required. 2. Adheres to Good Manufacturing Practices and standard operating procedures. 3. Weighs and checks raw materials. Assembles, cleans, and sterilizes process equipment, monitors processes. 4. Completes electronic work instructions and maintains clean room environment to comply with regulatory requirements. 5. Operates primary production equipment within the assigned functional area (i.e. bioreactors, chromatography skids, media or buffer preparation equipment etc.) as instructed. 6. Effectively uses in process automation systems (i.e. Delta V and Syncade Interactions, Pi Vision) and some supporting business systems (i.e. SAP, Infinity, Maximo etc.) to maintain production records. 7. Revises and creates process documents with little to no instruction, assists with process related investigations. 8. Leads in maintaining material and components inventory level. 9. Assists with reviewing batch and exception reports associated with each manufacturing lot, in conjunction with supervisor and Quality representative. 10. Assists with area specific initiatives associated with work safety. Knowledge and Skill - High school diploma is required. Knowledge of science generally attained through studies resulting in a B.S., in science, engineering, biochemistry or related discipline, or its equivalent is desired but not required. - A minimum of 2+ years of process operations experience in a highly automated biotechnology manufacturing facility subject to Good Manufacturing Practices (GMP) regulations. - 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. - Maintains a professional and productive relationship with area management and co-workers. Working Conditions Work is performed in a state- of-the-art large scale cell culture facility with classified areas requiring appropriate personal protective equipment (PPE). These roles require some contact with hazardous materials such as caustic, and steam. 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: $29.83 - $36.15per 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

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