Qa Engineer • Mid-Level

Who you are

You have extensive knowledge of FDA QSR, ISO 13485, and ISO 14971, along with applicable worldwide regulations. Your strong communication skills enable you to effectively collaborate with cross-functional teams and suppliers at all levels within the organization. You are detail-oriented and committed to ensuring compliance and efficiency in quality management processes.

You have experience in developing and coordinating innovative solutions to quality and regulatory-related activities. Your ability to support international market expansion by controlling documentation and product release is crucial. You understand the importance of maintaining a compliant Quality Management System and are proactive in implementing new quality initiatives.

What you'll do

As a QMS Engineer, you will ensure efficient and compliant processes throughout the organization. You will support the preparation and hosting of external Quality System inspections, ensuring that all regulatory requirements are met. Your role will involve developing quality plans for the integration of new entities or devices into the QMS, as well as assisting in the development of Quality Agreements.

You will implement procedures and SOPs for QA/QC and ISO audits, ensuring that all processes align with regulatory requirements. Your responsibilities will also include providing quality oversight to cross-functional teams around the world, ensuring that quality standards are upheld in all operations.

What we offer

Revance offers a collaborative work environment where you can make a significant impact on the quality of medical devices. You will have the opportunity to work closely with various teams and contribute to the strategic direction of the organization. We encourage you to apply even if your experience doesn't match every requirement, as we value diverse perspectives and backgrounds.