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Operator I
Aseptic Operations SIM Bulk Operations
Posted on 9/16/2022
INACTIVE
Locations
Phoenix, AZ, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Requirements
  • Robust functionality in Microsoft Applications and other computer based systems utilized in the manufacturing department (i.e. MES, HMI's, etc.)
  • Demonstrated proficiency in the ability to gown into applicable controlled areas per area classification specific requirements
  • Intermediate written and verbal communication skills within the department and with support groups
  • Functional job specific proficiency in mathematics
  • Practical understanding of specialized manufacturing equipment operational theory used for the manufacturing of sterile injectable products
  • Ability to pass a full physical including a respiratory certification with annual monitoring
  • Ability to stand up to 8 hrs/day, utilizing controlled movements
  • Aptitude to use hand tools in the setup and trouble-shooting of specialized manufacturing equipment
  • Ability to execute complex activities both independently and in a team environment
  • High school diploma or equivalent required
  • 1 year of relevant work experience required, preferably in a regulated and/or pharmaceutical environment
  • An equivalent combination of education/experience may substitute
Responsibilities
  • Accomplishes manufacturing activities per detailed procedural guidance with a demonstrated attention to detail
  • Performs handling of hazardous materials in compliance with site, industry, local, and federal regulations
  • Maintains manufacturing environmental conditions (Non-Viable Particulate(s) and Viable microbial levels per controlled area classification specifications) by performing area disinfection regiment as required to meet global Health Authority requirements
  • Executes specialized responsibilities mandated by detailed written procedures, site, industry, local, and federal regulations
  • Assures and completes detailed documentation that is a correct and accurate record. Addresses procedural /documentation errors expeditiously and effectively
  • Continuously updates job knowledge by participating in job specialized training requirements
  • Participates as a contributing member in CI projects
  • Consistently projects a positive attitude and example for other department team members/operators to emulate
  • Performs other tasks as assigned
Bristol-Myers Squibb

10,001+ employees

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