Job Details

Bioprocess Associate Upstream Clinical Manufacturing: M Th: 7a 5p

Company name
Bristol-Myers Squibb Company

Devens, MA

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Bioprocess Associate - Upstream Clinical Manufacturing: M-Th: 7a-5p





Bioprocess Associate - Upstream Clinical Manufacturing: M-Th: 7a-5p



Job Number:


Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. One shared journey is moving us forward at Bristol-Myers Squibb. Around the world, we are passionate about making an impact on the lives of patients with serious disease. Empowered to apply our individual talents and ideas so that we can learn and grow together, we are driven to make a difference, from innovative research to hands-on community support. 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 the resources to pursue their goals, both at work and in their personal lives.

Reporting to the Shift Supervisor, Devens Clinical Manufacturing, the Bioprocess Associate of Upstream Clinical Manufacturing is responsible for advancing the mid to late stage clinical pipeline according to established work instructions and in accordance with current Good Manufacturing Practices (cGMPs). The Clinical Manufacturing Building (CMB) is a brand new, state of the art facility utilizing single-use technology.

Key responsibilities include:

-Weighs and checks raw materials.

-Assembles, cleans and autoclaves process components.

-Assists in maintaining material and component inventory levels.

-Trains for proficiency in the operation of primary production equipment to complete process steps including media preparation, aseptic transfers, and cell culture and harvest operations in a clean room environment.

-Adheres to Good Manufacturing Practices and standard operating procedures.

-Recognize deviations from accepted practice and report to supervision.

-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.

-Trains for proficiency with process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP. Trackwise, Maximo etc.) to maintain production records.

-Assists with reviewing batch and exception reports associated with each manufacturing lot, in conjunction with supervisor and Quality representative.

-Provide assistance for areas specific initiatives associated with work safety



-Knowledge of science generally attained through studies resulting in a B.S., in engineering, biochemistry or science related discipline is desired but not required.

-Prior experience where attention to detail and personal accountability were critical to success

-Prior evidence of successful participation on work/study teams where combined contribution, collaboration, and results were expected.

-Maintains a professional and productive relationship with area management and co- workers.

-Demonstrates good interpersonal skills, is attentive and approachable.

-Takes responsibility for personal safety and contributes to establishing a safe workplace environment.

-Demonstrated proficiency in common computer tools such as word processing, spreadsheet and web based applications.

Position is 40 hours a week / 4-10 hour days / Monday - Thursday with some weekend work required.

Bristol-Myers Squibb is an equal opportunity employer - Minorities/Females/Protected Veterans/Disabled

Job: Prod/Process Equipment - Operator

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Bristol Myers Squibb

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Company info

Bristol-Myers Squibb Company
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Company Profile
Bristol-Myers Squibb is a global BioPharma company firmly focused on its Mission to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.

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