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Senior Bioprocess Associate
Night
Posted on 8/11/2022
INACTIVE
Locations
Devens, MA, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Management
SAP
Requirements
  • 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 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
Responsibilities
  • 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
  • Adheres to Good Manufacturing Practices and standard operating procedures
  • Weighs and checks raw materials. Assembles, cleans and sterilizes process equipment, monitors processes
  • Completes work instructions and maintains clean room environment to comply with regulatory requirements
  • Operates primary production equipment within the assigned functional area (i.e. bioreactors, chromatography skids, media or buffer preparation equipment etc.) as instructed
  • Effectively uses in 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
  • Revises and creates process documents with little to no instruction, assists with process related investigations
  • Leads in maintaining material and components inventory level
  • 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
Bristol-Myers Squibb

10,001+ employees

Biopharmaceutical development company
Company Overview
Bristol-Myers Squibb engages in the discovery, development, licensing, manufacturing, marketing, distribution and sale of pharmaceuticals.