On-Site Analytical Method Development Chemist

Omnient Labs; Tempe (AZ); On-site; USD 60,000 - 70,000; Full time

Benefits offered by this job

Medical, Dental, Vision

401(k) matching

PTO and more

Job summary

Omnient Labs in Tempe, AZ is seeking a Method Development and Validation Chemist I to validate, optimize, and support analytical methods powering client testing services. This on-site role requires strong analytical skills and experience in chromatography and spectroscopy.

You will perform method validation, transfer, and optimization, train QC staff, and maintain compliant documentation under cGLP/cGMP guidelines in a fast-paced lab environment.

Qualifications

• Bachelor’s degree in chemistry or related field required.
• At least 1 year of method development experience in food or dietary supplements industry required.

Responsibilities

• Perform method validation, verification, and robustness studies for HPLC, UPLC, LC-MS/MS, HS-GC, GC-FID, HPTLC, UV-Vis, and FTIR methods.
• Assist with development of lower-complexity analytical methods for routine testing.
• Support method transfer activities for routine methods.
• Perform method optimization to improve robustness and efficiency.
• Train QC chemists and provide routine technical support.
• Execute non-routine testing of R&D materials using established methods and summarize results.
• Maintain well-documented laboratory notebooks and ensure compliance with cGLP and cGMP.

Skills

Method development

Validation

Data analysis

Documentation

Education

Bachelor's degree in Chemistry

Biochemistry or Molecular Biology background

Tools

HPLC/UPLC

LC-MS/MS

HS-GC

GC-FID

HPTLC

UV-Vis

FTIR

Job description

Omnient Labs in Tempe, AZ is seeking a Method Development and Validation Chemist I to validate, optimize, and support analytical methods powering client testing services. This on-site role requires strong analytical skills and experience in chromatography and spectroscopy.

You will perform method validation, transfer, and optimization, train QC staff, and maintain compliant documentation under cGLP/cGMP guidelines in a fast-paced lab environment.