Analytical QC Scientist – cGMP & Stability Focus

Olon USA; Kentucky; Hybrid; USD 75,000 - 100,000; Full time

Job summary

Olon USA is seeking a detail-oriented QC Associate Scientist to support analytical testing of materials and products in a cGMP-regulated laboratory in Ohio. The role covers testing across HPLC, GC, KF and more, data generation and review, and collaboration with QA, manufacturing, and clients.

The candidate should have a chemistry degree and 3+ years in a pharmaceutical QC lab, with experience in cGMP/GLP environments, and strong data and documentation skills.

Qualifications

• Bachelor's degree in Chemistry or related discipline.
• 3 years pharma analytical lab with BS, or 1 year with MS, or equivalent.
• Quality Control lab experience required.
• Experience in a cGMP and/or GLP environment required.

Responsibilities

• Perform analytical testing of materials and products using multiple techniques.
• Support stability programs and data generation for projects.
• Review data for accuracy, completeness, and GMP documentation.
• OOS/OOT investigations and CAPA support.
• Prepare and review protocols, reports, specifications, and methods.
• Coordinate sampling, testing, and data management activities.
• Ensure compliance with cGMP, GLP, ICH, FDA/EMA guidelines.

Skills

HPLC

GC

KF

XRD

NMR

ICP-MS

ICP-OES

Stability testing

Data analysis

Microsoft Word

Microsoft Excel

Cross-functional teamwork

Education

Bachelor's degree in Chemistry

Tools

Laboratory information systems

Microsoft Word & Excel

Job description

Olon USA is seeking a detail-oriented QC Associate Scientist to support analytical testing of materials and products in a cGMP-regulated laboratory in Ohio. The role covers testing across HPLC, GC, KF and more, data generation and review, and collaboration with QA, manufacturing, and clients.

The candidate should have a chemistry degree and 3+ years in a pharmaceutical QC lab, with experience in cGMP/GLP environments, and strong data and documentation skills.