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Senior Manufacturing Associate

Pharma Universe

Chicago, illinois


Job Details

Full-time


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Full Job Description

This is a night shift position requiring a strong commitment to aseptic techniques, adherence to cGMP standards, and the ability to excel in controlled manufacturing environments.

Key Responsibilities

  • Perform advanced manufacturing tasks, including:
    • Weighing and preparing materials.
    • Operating filtration systems and overseeing fermentation processes.
    • Conducting cell inoculation and harvest operations.
    • Utilizing chromatography systems and tangential flow filtration (TFF) equipment.
  • Execute in-process testing such as pH, conductivity, spectrophotometry, osmolality, and cell counts.
  • Prepare media and buffer solutions as required by production schedules.
  • Ensure precise documentation of all activities in batch records and logs.
  • Maintain and sanitize cleanroom environments; dispose of materials per protocols.
  • Identify and promptly report deviations or unexpected issues to supervisors.
  • Support process development teams with technology transfer initiatives.
  • Uphold safety and operational procedures at all times.

Qualifications

  • Education:
    An associate degree or higher in Biology, Chemistry, Biotechnology, or a related field is preferred. Equivalent industry experience (approximately 3 years in biologics manufacturing) will also be considered.
  • Skills & Knowledge:
    • Strong familiarity with GMP protocols and biotechnology operations, including aseptic filtration, fermentation, chromatography, and TFF processes.
    • Ability to troubleshoot basic equipment and process issues effectively.
    • Excellent attention to detail and the ability to follow detailed instructions.
    • Competence in working independently and collaboratively within a team.
    • Proficiency with software tools for word processing and data management.

Additional Requirements

  • Flexibility to work night shifts in a fast-paced manufacturing environment.
  • Commitment to meeting deadlines while maintaining high-quality standards.

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