Senior Lab Analyst: Method Dev & QC Lead

Threshold Enterprises

Scotts Valley (CA)

On-site

USD 3,400 - 78,000

Full time

6 days ago
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Job summary

Threshold Enterprises in Scotts Valley, CA is seeking a Laboratory Analyst III to perform hands-on analytical chemistry and microbiology lab work, data analysis, and documentation. You will lead and train other analysts, maintain equipment, and drive process improvements in a cGMP environment.

Responsibilities include method development/transfer using USP, Eu Ph, and AOAC guidelines, reviewing test results, and coordinating with QA and R&D to support company goals.

Qualifications

  • Excellent written / verbal skills and attention to detail.
  • Demonstrated team leadership and training skills
  • Demonstrated process improvement experience
  • Demonstrated professional work skills and attitude
  • 20/20 vision or corrected vision.
  • One + years of experience in laboratory and chromatography method development/adaptation (or other analytical instrument method adaptation/development experience) in an industrial or academic chemistry or biological laboratory or an equivalent education and/or experience.
  • Degree in Chemistry, Biology, Microbiology or equivalent experience (minimum 3-4 years analytical lab experience and operation of HPLC, LC-MS).

Responsibilities

  • Perform laboratory work, data analysis and documentation, and act as trainer for other Laboratory Analysts.
  • Lead method development/transfer activities and ensure compliance with cGMPs and FDA guidelines.

Skills

Leadership
Process improvement
Communication skills
Attention to detail
Lab experience
Vision (20/20)

Education

Degree in Chemistry, Biology or Microbiology

Tools

HPLC
LC-MS
TLC
GC
ICP-MS
FT-IR
UV-Vis

Job description

Threshold Enterprises in Scotts Valley, CA is seeking a Laboratory Analyst III to perform hands-on analytical chemistry and microbiology lab work, data analysis, and documentation. You will lead and train other analysts, maintain equipment, and drive process improvements in a cGMP environment.

Responsibilities include method development/transfer using USP, Eu Ph, and AOAC guidelines, reviewing test results, and coordinating with QA and R&D to support company goals.

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