
Transforming aesthetics with advanced biotechnology solutions
Revance Therapeutics, headquartered in Nashville, Tennessee, specializes in biotechnology with a focus on aesthetic and therapeutic products. Their flagship product, DaxibotulinumtoxinA, is a next-generation neuromodulator designed for both aesthetic and therapeutic applications. Revance has raised ...
Revance offers competitive salaries, equity options, generous PTO, and a flexible remote work policy to support work-life balance....
Revance fosters a culture of innovation and scientific excellence, encouraging employees to contribute to groundbreaking advancements in biotechnology...

Revance • Johnson City, TN
Revance is hiring a QA Specialist for Manufacturing Quality Assurance to ensure compliance with cGMP and SOPs. You'll perform in-process quality checks and assist in batch record reviews. This entry-level role requires a focus on quality systems in a pharmaceutical environment.
You are an entry-level QA Specialist with a keen interest in manufacturing quality assurance. You understand the importance of compliance with cGMP and SOPs, and you are eager to learn and build your technical expertise in pharmaceutical quality systems. You are detail-oriented and committed to maintaining product quality and patient safety.
You have a foundational understanding of quality assurance processes and are ready to support manufacturing, filling, and packaging operations. You are comfortable working under the guidance of senior QA staff and are enthusiastic about performing in-process quality checks and assisting in batch record reviews.
You are proactive in documenting inspection activities in accordance with Good Documentation Practices (GDP) and company procedures. You are willing to participate in deviation documentation and investigations, contributing to the overall quality assurance efforts of the team.
In this role, you will provide on-the-floor support to manufacturing operations, ensuring compliance with established procedures. You will perform quality checks during manufacturing, filling, and packaging activities, including weight checks, seal integrity checks, line clearance verification, cleaning verification, and label reconciliation. Your attention to detail will be crucial as you document inspection activities accurately.
You will assist in the review of executed batch records for completeness and accuracy, supporting QA oversight of equipment set-up and clearance activities under supervision. You will participate in deviation documentation and investigations, helping to maintain high standards of quality and compliance.
Additionally, you will aid in the preparation and revision of SOPs and controlled documents, ensuring that all documentation meets regulatory requirements. You will collaborate closely with senior QA staff and other team members to uphold the quality assurance standards of the organization.
Revance offers a supportive environment for entry-level professionals to grow their careers in quality assurance. You will have the opportunity to learn from experienced QA staff and gain hands-on experience in a manufacturing setting. The company values compliance and quality, providing you with the tools and resources needed to succeed in your role. You will be part of a team dedicated to maintaining product quality and patient safety, contributing to the overall mission of the organization.
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