Bristol Myers Squibb Single Use Facility Bioprocess Associate in Devens, Massachusetts
At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.
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.
This position is Third Shift Monday through Thursday 9:30PM to 7:30AM.
Operate production equipment within an assigned functional area adhering to Good Manufacturing Practices and standard operating procedures.
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. Weigh and check raw materials.
Support a safe work environment and contribute to area specific initiatives associated with work safety.
Weighs and checks raw materials. Assembles, cleans and autoclaves process components. Assists in maintaining material and component inventory levels.
Works on routine manufacturing assignments per written procedures that are moderately complex with minimal instructions. Assists in revising and creating process documents, i.e. SOP’s and Batch Records, and assists with process related investigations.
High school diploma is required.
Knowledge of science generally attained through completion of a certificate program or Associates Degree in Biotechnology or a related field is 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.
Prior experience with Good Manufacturing Practices (GMP) regulations and/or prior work experience in a clean room or highly regulated environment desired.
Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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.
Company: Bristol Myers Squibb
Req Number: R1532810-en-us
Updated: 2020-11-28 03:09:24.064 UTC
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
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