Quality Assurance (QA) Specialist III

Who you are

You have advanced experience in quality assurance, demonstrating a strong ability to work independently and under minimal supervision. Your background includes hands-on QA experience, particularly in quality operations, ensuring compliance with both US and international regulatory requirements for biologic drug substances and drug products. You are comfortable interacting with cross-functional teams, including Materials Management, Validation, Quality Control, and Manufacturing, and you understand the importance of collaboration in achieving quality objectives.

You possess a keen eye for detail and are skilled in performing a wide variety of quality assurance activities. Your experience includes conducting incoming quality attribute inspections and reviewing documents such as standard operating procedures, master batch records, and packaging and labeling records. You are adept at reviewing executed production batch records and associated documentation, including any deviation and investigation reports related to lot release.

Your ability to analyze and interpret complex quality data is complemented by your strong communication skills, allowing you to effectively convey quality-related information to various stakeholders. You are committed to maintaining high standards of quality and compliance, and you thrive in environments where you can contribute to the continuous improvement of quality processes.

Desirable

Experience in biologics or pharmaceuticals is a plus, as is familiarity with regulatory requirements specific to these industries. You may also have knowledge of quality management systems and methodologies that enhance quality assurance practices.

What you'll do

In this role, you will be responsible for providing quality assurance support to CMC teams and in-house production. You will perform a variety of quality assurance activities to ensure compliance with Revance procedures and applicable regulatory requirements. This includes conducting inspections of incoming raw materials and reviewing documentation related to production and quality control.

You will collaborate with cross-functional teams to ensure that quality standards are met throughout the production process. Your responsibilities will include reviewing standard operating procedures, master batch records, and packaging and labeling records to ensure accuracy and compliance. You will also be involved in the review of executed production batch records and associated documentation, ensuring that all deviations and investigations are properly documented and addressed.

Your role will require you to stay updated on industry best practices and regulatory changes, allowing you to contribute to the continuous improvement of quality assurance processes. You will play a key role in maintaining a culture of quality within the organization, ensuring that all team members understand the importance of compliance and quality standards.

What we offer

Revance offers a competitive salary range of $90,000 - $105,000 annually, along with an annual performance bonus. You will have the opportunity to work in a collaborative environment where your contributions to quality assurance will have a direct impact on the success of our products. We value our employees and are committed to providing a supportive workplace that fosters professional growth and development. Join us in our mission to deliver high-quality biologic products that improve patient outcomes.