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Analytical Chemist – Method Development & Validation

Job in Cincinnati, Hamilton County, Ohio, 45208, USA
Listing for: Astrix Inc.
Contract position
Listed on 2026-07-16
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 28 - 31 USD Hourly USD 28.00 31.00 HOUR
Job Description & How to Apply Below

Analytical Chemist – Method Development & Validation

Pay Rate Low: 28 | Pay Rate High: 31

At this time, Astrix cannot transfer nor sponsor a work Visa for this position.

Relocation assistance is not available for this position.

Join a team where your analytical expertise drives quality and innovation. This role offers a diverse mix of laboratory testing, method validation, instrumentation support, regulatory compliance, and collaboration with manufacturing, quality, and R&D teams.

Pay: $28-$31/hr

Schedule: Mon-Fri 8a-5p

Type of Job: Contract 2–3-month assignment with possibility of extension and/or permanent employment

Location: Cincinnati, OH

Benefits Offered: Medical/dental coverage! Weekly pay!

Daily Tasks:

What you will do:
  • Develop, validate, optimize, and maintain analytical test methods.
  • Perform testing using HPLC, GC, GC-MS, LC-MS, FTIR, Karl Fischer, and other analytical techniques.
  • Troubleshoot analytical instruments and provide technical support to laboratory teams.
  • Support method transfers, laboratory training, and continuous improvement initiatives.
  • Prepare technical reports, validation documentation, and laboratory records.
  • Collaborate with internal teams and external partners to support product quality, process improvements, and regulatory compliance.
  • Ensure laboratory activities comply with GLP, ISO, and company quality standards.
Qualifications/Requirements:
  • Bachelor's degree in Chemistry or a related scientific field (advanced degree preferred).
  • 5+ years of analytical chemistry experience in a quality, R&D, or regulated laboratory environment.
  • Hands‑on experience with analytical instrumentation, including HPLC, GC, GC-MS, LC-MS, IC, FTIR, Karl Fischer, pH, titrations, and wet chemistry.
  • Experience developing, validating, optimizing, and transferring analytical test methods.
  • Knowledge of GLP, ISO 9001, Quality Management Systems, and regulatory compliance.

We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

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