Bioprocess Associate

About the role

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.

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