Aliquoting Technician – Precision Liquid Handling

Job Description

The Aliquoting Technician handles the most volume-sensitive work we do. You’ll dispense reagents, buffers, controls, and client-supplied materials into vials, tubes, and cartridges to exacting specifications – often in the microliter range, often on materials that are expensive, limited in supply, or time-sensitive.

You’ll work with manual and semi-automated liquid handling equipment, verify calibration before each run, and document volumes, lot assignments, and environmental conditions as you go. Because many of these materials are temperature-sensitive, you’ll manage staging, cold storage, and transfer timing so nothing sits outside its validated range.

This role sits at the intersection of laboratory technique and production discipline. You’ll be running batches, not one-off experiments – but the pipetting standard is a lab standard, and it doesn’t relax because the count is high.

Job Requirements

Candidates should bring genuine hands-on liquid handling experience and the patience for precise, repetitive technique. Comfort with aseptic practice and an understanding of why cold chain matters are both essential. If you’ve worked a clinical or research bench and want production-scale work in a structured environment, this is a strong fit.

Required qualifications:

  • Associate degree or higher in a life science field, or equivalent laboratory experience
  • Demonstrated proficiency with manual pipetting and precision liquid transfer
  • Understanding of aseptic technique and contamination control
  • Ability to work within a cleanroom gowning protocol
  • Meticulous documentation of volumes, lots, and process conditions
  • Comfort working with cold-stored and temperature-sensitive materials

Preferred qualifications:

  • Experience with semi-automated or automated liquid handling systems
  • Background in clinical diagnostics, biotech, or reagent manufacturing
  • Familiarity with equipment calibration and verification procedures
  • Exposure to ISO 13485 or cGMP documentation practices

 

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