Cosmetics Analytical Chemist (GC/HPLC) – Quality Control

Ignite Human Capital•Milwaukee, WI
•$25 - $40•Onsite

About The Position

The Analytical Chemist performs hands-on quality control testing and releases raw materials, bulk products, and finished goods requiring GC/HPLC and other analytical testing. The role is part of the QC team, reports to the QC Manager, and works closely with production and other departments to help ensure products move on time and remain compliant. The chemist is responsible for maintaining instruments, data, and documentation. This is a full-time, non-exempt, 100% onsite position in Milwaukee, Wisconsin, scheduled for second shift/mid-shift. Compensation is $25–$40 per hour, depending on experience, plus a shift differential and eligibility for an annual bonus. The employer is an established contract manufacturer of personal care and consumer products, with more than 30 years in business and two U.S. manufacturing facilities. Its product portfolio includes skin care, cosmetics, household, pet, and medical products. The company has grown substantially and is investing in expanded capabilities and capacity, while maintaining a family-oriented, people-first culture.

Requirements

  • Bachelor's degree in Chemistry or a related science.
  • 2–4+ years of hands-on HPLC and GC experience in a GMP-regulated environment.
  • Strong analytical, statistical, and problem-solving skills.
  • Excellent written and verbal communication in English.
  • Organized, detail-oriented, and self-directed, with good time management.
  • Proficiency with Microsoft Office.

Nice To Haves

  • Method validation experience.
  • Background in personal care, cosmetics, OTC, pharmaceutical, or consumer products manufacturing.

Responsibilities

  • Test and release all materials requiring GC/HPLC analysis, with proper identification and documentation.
  • Maintain and calibrate GC/HPLC and other laboratory equipment, and perform minor repairs as needed.
  • Develop, modify, and validate test protocols and analytical methods to meet FDA/GMP requirements.
  • Produce and maintain complete, accurate testing records.
  • Support routine testing of raw materials, bulk products, and filled goods as needed.
  • Practice and monitor GMP compliance and safety procedures in the laboratory and on the manufacturing floor.
  • Contribute ideas to improve laboratory processes and support other QA/QC areas as needed.

Benefits

  • Shift differential.
  • Annual bonus eligibility.
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