Quality Control Scientist

Integrated Resources, Inc ( IRI ); North Carolina; On-site; USD 60,000 - 75,000; Full time

Job summary

Integrated Resources, Inc (IRI) is seeking a QA/QC analyst to perform routine analytical testing on APIs, intermediates, and finished products in a GMP-regulated lab. You will operate HPLC, GC, UV-Vis, IR, and Karl Fischer instruments and ensure precise data logging.

Ideal candidates hold a Bachelor’s degree in Chemistry with 1–3 years of pharmaceutical lab experience and a strong eye for accuracy, documentation, and regulatory compliance.

Qualifications

• Bachelor’s degree in Chemistry or related field.
• 1–3 years in pharmaceutical QA/QC preferred.
• Experience with analytical testing and instrumentation.

Responsibilities

• Conduct routine lab analyses of APIs, excipients, and finished products.
• Perform HPLC, GC, UV-Vis, IR, and Karl Fischer testing.
• Maintain accurate records per GDP and cGMP standards.
• Prepare SOPs and assist in method development/revision.
• Monitor stock of chemicals and calibrate instruments per schedule.

Skills

Analytical chemistry

Quality control

GxP compliance

Laboratory documentation

Education

Bachelor's degree in Chemistry

Tools

HPLC

GC

UV-Vis Spectrophotometer

IR Spectrophotometer

Karl Fischer Titrator

Particle Size Analyzer

Bulk Density Tester

Job description

• Conduct routine laboratory analysis of pharmaceutical raw materials, active pharmaceutical ingredients (APIs), in-process samples, finished dosage forms, and stability samples in accordance with approved testing methods and applicable pharmacopoeial standards.
• Perform analytical testing using laboratory instruments such as HPLC, GC, UV-Visible Spectrophotometer, IR Spectrophotometer, Karl Fischer Titrator, Particle Size Analyzer, and Bulk Density Tester.
• Ensure accurate recording, verification, and maintenance of laboratory results, raw data, and analytical records in compliance with Good Documentation Practices (GDP).
• Execute assigned analytical activities independently while ensuring adherence to approved methods, testing schedules, and quality requirements.
• Support the preparation, revision, and review of analytical test methods, Standard Operating Procedures (SOPs), and laboratory protocols.
• Carry out routine instrument checks, calibration, and preventive maintenance activities in accordance with approved procedures and training requirements.
• Monitor laboratory stock levels and coordinate the availability of chemicals, reagents, volumetric solutions, and other essential testing consumables.
• Assist in laboratory investigations, analytical discrepancies, out-of-specification (OOS) results, and troubleshooting activities under the guidance of senior team members.
• Review laboratory worksheets, analytical reports, and supporting documentation to ensure completeness, accuracy, and compliance.
• Maintain laboratory cleanliness, safety standards, and proper chemical handling and disposal practices while following cGMP, cGLP, and applicable regulatory requirements.

Educational Qualification

• Bachelor’s degree in Chemistry or another relevant scientific discipline. A Chemistry background is preferred.

Experience & Technical Skills

• 1–3 years of relevant experience in the pharmaceutical industry.
• Prior experience in Quality Control or pharmaceutical analytical laboratories is preferred, particularly within the generic drug manufacturing sector.
• Hands‑on exposure to analytical testing techniques and laboratory instrumentation.