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Manufacturing Associate II, Reagents

United States, Northbrook Employment contract 26.00 - 32.00 USD / Hour · Job Posted May 30, 2026
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Job Responsibility

  • Deliver manufacturing requirements and attainment of production schedule for standard inventory, build-to-order, and contract manufacturing market products
  • Deliver manufacturing requirements for qualification/processing of incoming materials, production intermediates, and stability samples
  • Deliver timely and accurate completion of manufacturing sections of process documentation and related business system transactions
  • Deliver timely and accurate completion of inventory cycle counts
  • Document non-conformances and participate in Material Review Board
  • Support design transfer and integration of new products and processes
  • Support process development and process improvements
  • Participate in the writing and execution of equipment and process validations
  • Support investigations and resolution of findings impacting the Reagent Manufacturing Organization identified through audits, non-conformances, corrective/preventive actions, or customer complaints escalation
  • Deliver timely maintenance and calibration of assigned Manufacturing measuring and monitoring devices
  • Monitor select non-inventory supplies, maintain focused supplies, and generate purchase requisitions as needed
  • Maintain cleanliness and integrity of manufacturing laboratory and storage areas
  • Participate in applicable departmental and interdepartmental training
  • maintain current and effective training to standard operating procedures, work instructions, and applicable changes affecting the Reagent Manufacturing
  • Assist in establishing annual performance goals
  • fulfill performance goals
  • Maintain effective and professional multi-level organizational interfaces
  • Maintain personal compliance and facilitate departmental compliance with the Quality System
  • Adhere to safety, disposal, and gowning requirements
  • Update work instructions and standard operating procedures as required
  • Perform change control as required to support change requirements including Engineering Change Orders, Document Change Control, and Deviations
  • Assist in executing projects targeting efficiency, cost reduction, and quality improvements within scope of Bioassay manufacturing processes
  • Support investigations and resolution of findings identified through audits, non-conformances, key performance indicator trends, corrective/preventive actions, or customer complaints escalation
  • Participate in task-specific training of new Reagent Manufacturing Associates
  • Other duties as assigned

Requirements

  • Associate's Degree Associates degree in Chemistry, Life Sciences, Biotechnology, or Medical Technology related field required
  • 3+ Years At least 3 years of relevant experience in a Life Sciences, Chemistry, Medical Technology, or Biotechnology industry required

Nice to have

  • Bachelor's Degree Bachelors Degree in Chemistry, Life Science, Biotechnology, or Medical Technology related field preferred
  • 1+ Years At least 1 year of relevant experience in an FDA regulated and/or ISO certified organization preferred

What we offer

  • health benefits
  • retirement and financial wellbeing
  • time off programs
  • wellbeing support and perks
  • annual incentive program

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