Micro Quality Control (Q/C) & Biology Analyst I or II

CLENE NANOMEDICINE INCNorth East, MD
$23 - $30Onsite

About The Position

We are seeking a detail-oriented and motivated Micro Quality Control (Q/C) & Biology Analyst I or II to join our team. In this role, you will organize and perform testing activities with accuracy and precision while minimizing workloads. The Micro Quality Control (Q/C) & Biology Analyst I or II follows all Standard Operating Procedures (SOPs), Test Methods (TSMs), Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and internal processes.

Requirements

  • Bachelor's degree in microbiology/biology, or another related science field preferred.
  • One (1) to four (4) years' experience in a related field.
  • Equivalent combinations of education and relevant laboratory experience will be considered.
  • Exceptional analytical skill set and attention to detail.
  • Knowledge of USP testing procedures and FDS regulations.
  • Excellent computer skills, including, but not limited to, MS Office.
  • Excellent verbal and written communication skills with all levels.
  • Required to stand, walk, and talk or hear.
  • Ability to lift up to 50 pounds.
  • Ability to read and interpret documents such as, operating, maintenance, and procedure manuals.

Responsibilities

  • Perform and monitor testing activities.
  • Review and update work schedules to effectively maintain the testing schedule.
  • Review testing results to ensure report accuracy.
  • Coordinate testing plans to ensure materials are testing according to schedule.
  • Plan usage of laboratory materials to ensure optimal testing levels.
  • Work with management to address issues regarding testing, quality, and production.
  • Manage deadlines based on project expectations.
  • Track production and research to help predict future scheduling needs.
  • Gather, process, analyze, and share research and product test data.
  • Work with management to establish SOPs for testing, equipment, and laboratory procedures.
  • Work with management to establish test methods, validate products, and qualify technicians.
  • Ensure GMP/GLP equipment calibration and IOPQ (mapping) are current.
  • Assist in the acquisition and/or production, if required, of research-related materials.
  • Work with management to design and enact research procedures.
  • Participate in research and/or microbiology testing.
  • Analyze and present research data.
  • Perform other duties as assigned.

Benefits

  • Up to 4 weeks paid leave
  • Paid holidays
  • Medical, dental, vision, and prescription insurance for employees and eligible dependents
  • 401(k) retirement plan with employer match
  • Opportunities for professional grown and continued learning
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