QA Associate I - Process

Responsibilities

• Inspect material, components, and finished products against specified requirements
• Follow procedures to determine status or disposition and document results in records and lab notebooks
• Support manufacturing and QC units with inspections and material sampling
• Perform finished product inspections to ensure proper sampling prior to final release
• Provide process oversight support to manufacturing and ensure proper storage of materials
• Initiate deviations and complete immediate corrective actions
• Participate in monthly quality and safety walkthroughs

Requirements

• High school diploma, GED, or equivalent required
• Working knowledge of drug or device cGMP
• Proficiency with MS Word, Excel, and Access
• Ability to bend, squat, and lift a minimum of 30 pounds
• Ability to pass a physical and eye exam (including color vision)
• Ability to work 3rd shift (Sunday - Wednesday, 5:00 pm - 5:30 am)

Preferred Qualifications

• Associate’s degree
• Experience in a high-volume manufacturing environment
• Experience in a Quality Assurance capacity within the pharmaceutical or medical device industry

Benefits

• Competitive hourly pay with shift differential
• Comprehensive benefits package

About the Company

Tolmar is a pharmaceutical company dedicated to supporting the well-being of patients through ethical, compliant, and high-quality manufacturing processes. We value proactive engagement, continuous improvement, and accountability in everything we do.