The In Process Quality Assurance Auditor ensures product quality through independent inspections, testing, and auditing of pharmaceutical manufacturing and packaging within a cGMP environment.
They perform in-process inspections, verify documentation, identify non-conformances, and escalate issues to maintain compliance with FDA and DEA regulations.
The role supports continuous improvement by updating procedures, conducting audits, and training team members.
Qualifications include a high school diploma, 2+ years of QA experience in regulated pharma, knowledge of cGMP and regulatory standards, and proficiency with ERP systems.
Key skills involve critical thinking, attention to detail, communication, and teamwork.
Physical requirements include standing, lifting up to 50 lbs, and working in manufacturing environments.
All employees must adhere to a nicotine-free policy and work in a compliant, safe environment.