Quality Assurance Specialist

Role: Entry-level Manufacturing Quality Assurance (MQA) Specialist supporting pharmaceutical manufacturing, filling, and packaging to ensure cGMP and regulatory compliance. Responsibilities: perform in-process quality checks (e.g., weight, seal integrity, line clearance), review batch records, assist in deviation investigations, support equipment set-up oversight, and contribute to SOP updates. Requirements: High School diploma (Associate degree preferred), 0-2 years in QA or regulated industry, basic understanding of cGMP, proficiency in Microsoft Office, strong attention to detail, and teamwork skills. High-Value: pharmaceutical manufacturing, cGMP compliance, Good Documentation Practices, support during regulatory inspections, and calibration of measurement tools. Work setup: on-site in Johnson City, TN, with extended standing, occasional lifting, and protective gear use. May respond to critical shift issues outside scheduled hours.