Orano Med is seeking a detail-oriented QC Analyst - Raw Materials to join our Quality Control team. In this role, you'll be responsible for incoming quality control (IQC) activities for raw materials while providing cross-functional support to QC Chemistry operations and managing externally executed raw material testing projects in a GMP pharmaceutical environment. 

Routine Functions – QC

• Perform receipt, sampling, testing, and release of raw materials in compliance with GMP, USP, Ph. Eur., and internal procedures.
• Execute compendial and non-compendial testing using approved analytical methods.
• Review data and release materials using established quality systems.
• Maintain raw material specifications, sampling plans, and test methods.
• Manage material status labeling, quarantine, and inventory controls.
• Support and investigate material-related deviations, OOS/OOT results, and discrepancies.
• Serve as QC liaison for external laboratories performing raw material testing, including protocol review, data review, and issue resolution.
• Crosstrain and support routine QC chemistry testing as needed to meet operational demand.
• Maintain GMP documentation, logbooks, and reports.
• Other duties as assigned by Supervisor/Management

Continuous Improvement

• Promote a culture of safety, quality, and continuous improvement across the team.
• Identify process inefficiencies and lead improvement initiatives.
• Maintain strong knowledge of regulatory requirements (21 CFR Parts 11, 210, 211; ICH; USP).

Qualifications Required

Education

• Bachelor’s degree in Chemistry or a related technical field.

Experience

• 2–4 years of QC laboratory experience in a GMP-regulated environment, with at least 1–2 years in a Raw Material / IQC environment.
• Analytical instruments: HPLC, ICP-MS, GC, Titration, FTIR, pH/Osmometers, TOC / Conductivity, Endotoxin Testers
• USP methods & ICH guidelines
• Following detailed SOPs; meticulous execution/documentation (GDP)
• QMS in regulated environment