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Process Scientist I

United States, Stillwater, Minnesota 61000.00 - 70000.00 USD / Year · Job Posted March 27, 2026
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Job Description

This position is responsible for material processing, reagent formulation, technical manufacturing, in-process and final quality control of reagents, components and in-vitro diagnostic products.

Job Responsibility

  • Perform material processing and reagent for formulation bulk intermediates and components
  • Determine reprocessing need for calibrator, controls, and conjugates with assistance
  • Perform Good laboratory practices - maintain clean workspace in QC and Reagent Prep labs. Contribute to group Reagent Prep and QC duties, including lab and equipment maintenance
  • Utilize SAP (kitting, ordering to Cost Center, assign expiration dates, etc.) to ensure correct dating, accounting, and flow through facility
  • Participate in inventory accountability - PSA count, cycle counts, accurate kitting, etc.
  • Perform in-process testing and final Quality Control for LIAISON products per established procedures using the LIAISON analyzer family
  • Assign calibrator values to optimize kit performance
  • Assign kit control ranges per established procedures
  • Monitor internal control supplies and manufacture new controls as needed
  • Perform second-checking to ensure accurate records
  • Follow regulatory requirements - follow document instructions and maintain reasonable documentation error rates
  • Ensure proper documentation by correcting errors noted in procedures and forms (ECO) with assistance
  • Perform tasks assigned in NCR/ Deviations and Validations
  • Perform tasks assigned in CAPA
  • Ensure safety of self and others by complying with all company safety policies, including use of PPE
  • Participate in team meetings and attend group training sessions
  • Monitor training required in SmartTrain and ensure timely completion of all company training requirements
  • Help with basic new employee training such as instrument use, basic software training, etc.
  • Contribute to business continuity or continuous improvement projects by suggesting improvements and completing assigned tasks
  • Complete assigned tasks related to investigations for root cause determination and troubleshoot product or process issues

Requirements

  • Associates degree in Chemistry, Biology or Medical Technology required
  • 1+ years of related laboratory experience and/or demonstrated competence within the in-vitro diagnostic industry
  • Basic understanding of immunology and immunoassay techniques
  • Ability to work in a regulated environment
  • Working knowledge of general lab equipment (e.g. pH meter, balances, mixers, etc.)
  • Working knowledge of MS Excel
  • familiarity with Google Suite
  • Basic understanding of statistical analysis
  • Advanced skills in: Math and calculations
  • Writing and documentation
  • Grasping complex concepts and solutions
  • Problem-solving and analytical skills

Nice to have

Bachelor's or Master's degree preferred in Chemistry, Biology, Medical Technology or related science field or a 2 year degree (i.e. MLT) with equivalent experience

What we offer

  • comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks
  • may be eligible to participate in an annual incentive program

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