Bioprocess Associate

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.

Position Summary 

The Bioprocess Associate uses current Good Manufacturing Practices (cGMPs) in the execution of commercial manufacturing processes for the manufacture of therapeutic proteins used in medicines that are revolutionizing the treatment of serious disease. 

Shift hours are TBD

Key Responsibilities 

• Operate production equipment within an assigned functional area adhering to Good Manufacturing Practices (GMPs) and standard operating procedures (SOPs) 

• Revise and create process documents and assist with process related investigations 

• Train for proficiency in process automation and supporting business systems and in the operation of primary production equipment within the assigned functional area 

• Lead in maintaining material and components inventory level 

• Support a safe work environment and contribute to area specific initiatives associated with work safety 

• Weigh and check raw materials 

• Assemble, clean and autoclave process components 

• Assist in maintaining material and component inventory level 

• Work on routine manufacturing assignments per written procedures that are moderately complex with minimal instructions 

• Assist in revising and creating process documents (i.e., SOPs and Batch Records) and assist with process related investigations 

Qualifications & Experience 

• Minimum high school diploma required; knowledge of science generally attained through completion of a certificate program or Associate Degree in Biotechnology or a related field desired 

• Prior experience with Good Manufacturing Practices (GMP) regulations and/or prior work experience in a clean room or highly regulated environment desired 

• Prior experience successfully participating on work teams where personal accountability, attention to detail, collaboration, and results were expected 

• Demonstrated proficiency in common computer tools and web-based applications 

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.

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: