Revance
Quality Assurance Specialist
Johnson City, TN · Junior
Sponsorship not specifiedDetected 1 day ago
GMPProblem Solving
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16Unrated
Cap-exempt (no lottery)0
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Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70
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About the role
- 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.
- Reporting to: Q uality Assurance Supervisor
Responsibilities
- 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.
- Support QA oversight of equipment set-up and clearance activities under supervision.
- Aid in the preparation and revision of SOPs and controlled documents.
- Perform other quality-related tasks as assigned by QA Management.
- Support regulatory inspections and customer audits by providing accurate information as requested.
- 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.
Requirements
- 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.
- Build proficiency in quality oversight practices and regulatory expectations through on-the-job training.
Nice to have
- 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),
- High School Diploma or equivalent required
Skills
- Learn and apply basic root cause analysis and problem-solving tools under the direction of senior QA personnel.
Company info
- Follow established procedures to ensure compliance with 21 CFR Parts 210/211, ICH guidelines, and company Quality Management System (QMS) requirements.
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