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Job Summary: The QA Specialist I – Manufacturing Quality Assurance (MQA)  is responsible for  providing on-the-floor support to manufacturing, filling, and packaging operations to ensure compliance with cGMP, SOPs, and applicable regulatory requirements. This entry-level role focuses on performing in-process quality checks,  assisting  in batch record review, and supporting deviation documentation under the guidance of senior QA staff. The Specialist I  helps   maintain  product quality, compliance, and patient safety by executing defined QA responsibilities and building technical  expertise  in pharmaceutical quality systems.     Reporting to: Q uality Assurance Supervisor Location: J ohnson City, TN Manufacturing Plan t Schedule: Mon-Fri 7:00AM - 4:30PM Responsibilities/Essential Duties: Perform quality checks during manufacturing, filling, and packaging activities, including weight checks, seal integrity checks, line clearance verification, cleaning verification, and label reconciliation.   Document inspection activities in accordance with Good Documentation Practices (GDP) and company procedures.   Assist in the review of executed batch records for completeness and accuracy.   Support QA oversight of equipment set-up and clearance activities under supervision.   Participate in deviation documentation and investigations under the guidance of2026-03-04 senior QA staff.   Aid in the preparation and revision of SOPs and controlled documents.   Perform other quality-related tasks as assigned by QA Management.   Follow established procedures to ensure compliance with 21 CFR Parts 210/211, ICH guidelines, and company Quality Management System (QMS) requirements.   Uphold GDP and data integrity standards during all inspection and documentation activities.   Escalate potential compliance issues to senior QA staff in a timely manner.   Support regulatory inspections and customer audits by providing accurate information as requested.   Demonstrate proficiency in inspection methodologies, measurement tools, and acceptance sampling standards (e.g., ANSI/ASQ Z1.4).   Gain working knowledge of cGMP manufacturing and packaging operations.   Learn and apply basic root cause analysis and problem-solving tools under the direction of senior QA personnel.   Build proficiency in quality oversight practices and regulatory expectations through on-the-job training.   Collaborate with operations staff to reinforce compliance and quality standards on the production floor.   Participate in quality training sessions to support professional growth and readiness for Level II responsibilities.   Basic Qualifications: High School Diploma or equivalent required; Associate degree in a scientific or technical discipline preferred.   Minimum 0–2 years of experience in Quality Assurance, Manufacturing, or a regulated industry (pharmaceutical/biotechnology preferred),   Basic understanding of cGMP and regulatory requirements for pharmaceutical production.   Proficiency with Microsoft Office applications (Word, Excel, PowerPoint).   Strong attention to detail, communication, and organizational skills.   Ability to follow procedures, take direction, and work collaboratively in a team environment   Company Summary: Revance is a global company developing, producing, and distributing industry-leading, differentiated products across aesthetics, skincare, and therapeutics. Revance drives innovation beyond convention to offer treatment options for indi