QC Associate Scientist

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

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QC Associate Scientist

Full Time Concord, OH, US

Associate Scientist, QC

Department: Quality

Position Summary

We are seeking a detail-oriented and proactive Associate Scientist, QC to support quality control and stability testing activities within a cGMP-regulated pharmaceutical laboratory. This role is responsible for performing analytical testing of raw materials, in-process samples, finished products, and stability samples; generating and reviewing analytical data; supporting laboratory investigations; and ensuring compliance with applicable regulatory requirements. The ideal candidate will have experience working with small molecule drug substances and drug products in cGMP and GLP environments.

• Perform analytical testing of raw materials, in-process samples, finished products, and stability samples using techniques such as HPLC, GC, KF, FTIR, XRD, DSC, TGA, PSD, NMR, ICP-MS, ICP-OES, and other laboratory instrumentation as required.
• Support stability programs through sample management, stability chamber monitoring, testing, and generation of stability data.
• Coordinate timely and compliant generation of analytical data to support client projects and manufacturing operations.
• Review laboratory data for technical accuracy, completeness, compliance, and adherence to good documentation practices.
• Conduct OOS, OOT, and laboratory investigations and support implementation of corrective and preventive actions (CAPAs).
• Author and review protocols, reports, specifications, analytical methods, and related laboratory documentation.
• Perform raw material sampling, testing, inspection, and coordination activities as required.
• Manage laboratory inventory, retained samples, reagents, standards, chemicals, and associated laboratory systems.
• Collaborate with Quality Assurance, Manufacturing, and Clients to support analytical testing, batch release, and stability studies.
• Maintain compliance with cGMP, GLP, ICH, FDA, EMA, and other applicable regulatory requirements.
• Other duties as assigned.

Qualifications

Education and Experience

• Bachelor's degree in Chemistry or a related scientific discipline required.
• Minimum of 3 years of related pharmaceutical analytical laboratory experience with a B.S. degree, or 1 year with an M.S. degree, or an equivalent combination of education and experience.
• Relevant experience in a Quality Control laboratory is required.
• Experience working in a cGMP and/or GLP-regulated environment is required.

Skills and Competencies

• Proficiency with standard laboratory equipment, including HPLC, KF, XRD, PSD, analytical balances, pipettes, pH meters, and titration systems is required.
• Experience with GC, FTIR, UV-Vis, DSC, TGA, IC, ICP-MS, and ICP-OES is preferred, but not required.
• Experience with assay, impurity, raw material, and stability testing.
• Familiarity with ICH stability guidelines and pharmaceutical quality systems.
• Experience conducting OOS/OOT investigations and root cause analysis preferred.
• Strong proficiency in Microsoft Word and Excel.
• Strong written and verbal communication skills and the ability to work effectively with clients and cross-functional teams.
• Ability to manage multiple priorities and work effectively in a fast-paced environment.
• Strong understanding of chemistry principles, data analysis, and basic statistical concepts.