Associate Scientist-IVD Test Development

100% onsite

Cleveland, OH 44101

2436

JGERBER

Job Overview

We are seeking a highly motivated Associate Scientist with experience or interest in in vitro diagnostic (IVD) assay development to join our dynamic team. The successful candidate will perform laboratory work, data analysis, under the guidance of a supervisor. This role requires hands-on execution of experiments, routine lab maintenance, and meticulous documentation to support product development, validation, and verification initiatives. The position involves handling human biological specimens, including blood, plasma, urine, and other bodily fluids, in compliance with all safety regulations and company policies.

Essential Duties & Responsibilities

  • Perform assigned laboratory testing under supervision with clear instructions
  • Conduct routine and semi-routine tasks with increasing independence
  • Execute laboratory techniques and experimental procedures according to defined protocols
  • Prepare reagents and solutions required for experiments
  • Carry out tests and procedures in accordance with standard protocols
  • Handle human biological specimens (e.g., blood, plasma, urine, and other bodily fluids) following biosafety guidelines and regulatory requirements
  • Perform routine maintenance and general laboratory upkeep
  • Accumulate, organize, and analyze experimental data
  • Document procedures, observations, and results accurately according to Company and GDP policy
  • Assist in preparing and presenting project data for internal discussions
  • Participate in technical discussions and project meetings
  • Ensure compliance with all safety and company policies
  • Perform all other duties as assigned

Qualifications

  • Education & Experience:
    • Bachelor’s degree in Biology, Biochemistry, Molecular Biology, Biomedical Engineering, or a related field with 1-4 years of relevant experience
    • Master’s degree with 0-1 years of experience
    • Industry experience preferable
  • Technical Skills:
    • Hands-on experience with standard laboratory techniques such as pipetting, reagent preparation, and handling (Experience with automated immunochemistry analyzers preferred)
    • Ability to follow standard protocols and troubleshoot routine lab tasks
    • Experience with data analysis and documentation best practices
    • Familiarity working in an FDA or ISO-regulated environment is a plus
    • Proficient computer skills especially with Microsoft Office applications
  • Soft Skills:
    • Strong attention to detail and organizational skills
    • Effective communication and teamwork abilities
    • Ability to manage and prioritize workload effectively
    • Ability to work efficiently under supervision and follow instructions