QC Associate I - Incoming

Responsibilities

• Inspect incoming materials, components, and finished products against specified requirements.
• Perform physical or dimensional testing on materials such as labels, cartons, and containers using equipment like calipers and micrometers.
• Document all results in compliance with cGMP, ALCOA+, and data integrity policies.
• Enter data and results into LIMS and review COAs/COCs for compliance prior to material release.
• Identify and segregate non-conforming materials and initiate deviations for quality defects.
• Support materials management with sampling, inspection, and inventory requisitions.
• Maintain proper handling, storage, and traceability of all approved materials.
• Perform cleaning and monitoring of rooms and equipment, and coordinate equipment calibration.

Requirements

• High school diploma or GED required.
• Working knowledge of drug or device cGMP.
• Proficiency with MS Office (Word, Excel, PowerPoint, and Access).
• Ability to lift a minimum of 30 pounds.
• Ability to see color and pass a physical and eye exam.
• Ability to bend, squat, and work in office, warehouse, and laboratory environments.

Preferred Qualifications

• Associate’s degree or completion of college-level courses.
• Experience working in a high-volume manufacturing or laboratory environment.

About the Company

Tolmar is a pharmaceutical company dedicated to improving patient lives through high-quality products. We operate with a culture of engagement, accountability, and continuous improvement, placing people at the heart of our actions.