QC Analyst — GMP Lab for Skincare Innovation

iS CLINICAL

Mesa (AZ)

On-site

USD 55,000 - 75,000

Full time

14 days+
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Benefits offered by this job

401k
Life
Dental
Vision
Health
PTO

Job summary

Innovative Skincare in Mesa, AZ is seeking a Quality Control Analyst to test raw materials, in-process batches, and finished products for GMP compliance. You'll perform laboratory analyses, maintain documentation, and ensure adherence to SOPs and safety procedures.

This on-site role requires a Bachelor's degree in Chemistry or related science and 1–3 years of GMP-regulated laboratory experience. You will calibrate equipment, record results, and collaborate with QC/QA and Production teams to

Qualifications

  • Bachelor’s degree in Chemistry, Biology, or related science required.
  • 1–3 years of laboratory or QC experience in GMP-regulated setting preferred.
  • Strong documentation and regulatory compliance knowledge.

Responsibilities

  • Perform laboratory testing on raw materials, bulk, and finished products.
  • Follow established methods, SOPs, and GMP requirements.
  • Record, analyze, and report test results accurately.
  • Maintain and calibrate lab equipment as needed.
  • Document all work in lab notebooks, logbooks, and electronic systems.
  • Report and help investigate any out-of-specification results.
  • Support stability studies and related lab activities.
  • Work with QC, QA, and Production teams to resolve quality issues.
  • Maintain a clean, safe, and compliant laboratory environment.

Skills

Attention to detail
Documentation accuracy
Communication skills
GMP knowledge
Laboratory testing

Education

Bachelor's degree in Chemistry, Biology, or related science

Tools

pH meters
Viscometers
Spectrophotometers
Balances

Job description

Innovative Skincare in Mesa, AZ is seeking a Quality Control Analyst to test raw materials, in-process batches, and finished products for GMP compliance. You'll perform laboratory analyses, maintain documentation, and ensure adherence to SOPs and safety procedures.

This on-site role requires a Bachelor's degree in Chemistry or related science and 1–3 years of GMP-regulated laboratory experience. You will calibrate equipment, record results, and collaborate with QC/QA and Production teams to

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