GMP Pharmaceutical Chemist — Method Development & Validation

Indotronix Avani Group; Cincinnati (OH); On-site; USD 60,000 - 80,000; Full time

Job summary

Indotronix Avani Group is seeking a QA/Analytical Chemist with 2–3+ years of pharmaceutical GMP laboratory experience to support development and manufacturing through analytical testing, method development and validation, data analysis, and troubleshooting. The role requires a Bachelor’s degree in Chemistry or Biochemistry and hands-on experience with HPLC/UPLC, GC/GC-MS, and dissolution testing.

You will work under GMP/GLP guidelines, maintain documentation, and contribute to

Qualifications

• 2–3+ years pharmaceutical GMP lab experience required.
• Bachelor’s degree in Chemistry, Biochemistry, or related field.
• Experience with HPLC/UPLC for assay and related substances.
• Experience with GC/GC-MS and chromatographic troubleshooting.
• Dissolution testing and Oral Solid Dosage (OSD) experience.
• Analytical method development and validation.
• Experience with validation parameters: accuracy, precision, linearity, filter studies, solution stability.
• Strong knowledge of GMP, GLP, SOPs, and pharmaceutical regulations.

Responsibilities

• Support pharmaceutical development and manufacturing through analytical testing, method development/validation, data analysis, and laboratory troubleshooting.
• Ensure compliance with GMP, GLP, SOPs, and regulatory requirements.
• Perform analytical method development and validation studies and document results.
• Operate and troubleshoot laboratory instruments (HPLC/UPLC, GC/GC-MS, dissolution testers).
• Assist in troubleshooting analytical issues and data interpretation.

Skills

GMP lab experience

HPLC/UPLC

GC/GC-MS

Dissolution testing

OSD experience

Analytical method development

Method validation

Validation parameters

Laboratory troubleshooting

Empower

GMP knowledge

Regulatory compliance

Education

Bachelor's in Chemistry or Biochemistry

Tools

Empower

Job description

Indotronix Avani Group is seeking a QA/Analytical Chemist with 2–3+ years of pharmaceutical GMP laboratory experience to support development and manufacturing through analytical testing, method development and validation, data analysis, and troubleshooting. The role requires a Bachelor’s degree in Chemistry or Biochemistry and hands-on experience with HPLC/UPLC, GC/GC-MS, and dissolution testing.

You will work under GMP/GLP guidelines, maintain documentation, and contribute to