Quality Assurance Specialist - Medical Device

Role: QA Specialist responsible for ensuring quality compliance on the production floor for a medical device company. Primary objectives include conducting audits, product inspections, batch record reviews, and deviations management to support product release and regulatory adherence. Responsibilities encompass performing QA checks, line clearance, incoming material inspection, verifying regulatory compliance, and assisting with training and investigations. Qualifications: 0-2 years in QA, manufacturing, or regulated industry; knowledge of cGMPs and regulatory standards; proficiency in Microsoft Office; strong communication and organizational skills; ability to stand for extended periods and lift up to 20 lbs. High-Value: Medical device manufacturing, quality assurance, cGMP compliance, batch record review, regulatory adherence, in-process and incoming inspection, role located in Johnson City TN with Monday-Friday hours. Collaboration/reporting to QA Manager; no travel specified.