Quality Control Analyst

United Pharma; Indiana (PA); On-site; USD 65,000 - 90,000; Full time

Job summary

United Pharma is seeking a QC Analyst to support laboratory testing, GMP compliance, and quality control activities within a pharmaceutical manufacturing environment.

You will perform chemical, physical, and analytical testing of raw materials, in-process samples, and finished products using HPLC, GC, UV-Vis, and dissolution methods, with strong documenation of results and data review.

Qualifications

• Bachelor’s degree required in a relevant science field.
• 2+ years of QC/analytical laboratory experience in Pharma/Biotech/Life Sciences.
• Hands-on with HPLC, GC, and common laboratory instrumentation.
• Strong GMP/GLP knowledge and analytical testing practices.
• Experience with OOS/OOT investigations and deviations preferred.

Responsibilities

• Perform chemical, physical, and analytical testing of materials and products.
• Execute testing using HPLC, GC, UV-Vis, dissolution, and other instruments.
• Review analytical data, identify deviations, and document results.
• Prepare and maintain laboratory records, test reports, and controlled documents.
• Support OOS/OOT investigations, deviations, CAPA, and change controls.
• Calibrate, maintain, and troubleshoot laboratory instrumentation.
• Follow GMP, GLP, SOPs, safety, and regulatory requirements.
• Assist in method validation, verification, and transfers.

Skills

Documentation

Communication

Analytical thinking

Problem solving

Team collaboration

Education

Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field

Tools

HPLC

GC

UV-Vis

Dissolution

Job description

We are looking for a QC Analyst to support laboratory testing, GMP compliance, and quality control activities in a pharmaceutical/biotech manufacturing environment.

Key Responsibilities:

• Perform chemical, physical, and analytical testing of raw materials, in-process samples, and finished products.
• Execute testing using HPLC, GC, UV-Vis, dissolution, and other laboratory instruments.
• Review analytical data, identify deviations, and document results accurately.
• Prepare and maintain laboratory records, test reports, worksheets, and controlled documents.
• Support OOS/OOT investigations, deviations, CAPA, and change controls.
• Perform instrument calibration, maintenance, and troubleshooting.
• Follow GMP, GLP, SOPs, safety, and regulatory requirements.
• Support method validation, verification, and analytical method transfers as needed.
• Maintain laboratory equipment, standards, reagents, and sample inventory.
• Collaborate with QA, Manufacturing, R&D, and other cross-functional teams.

Required Qualifications:

• Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
• 2+ years of QC/analytical laboratory experience in Pharma, Biotech, or Life Sciences.
• Hands-on experience with HPLC, GC, and laboratory instrumentation.
• Strong knowledge of GMP/GLP and analytical testing practices.
• Experience with OOS/OOT, deviations, and laboratory investigations preferred.
• Strong documentation, communication, analytical, and problem-solving skills.