What are the responsibilities and job description for the Quality Assurance Auditor position at Viltis?
We are looking for a Quality Assurance Auditor to support our clients' facilities in Hopewell, NJ. As a Quality Assurance Auditor, you will be responsible for conducting phase audits, data audits, and facility audits to ensure compliance with 21 CFR Part 58 regulations and Good Laboratory Practice (GLP) standards.
The ideal candidate will have hands-on experience with phase audits, data audits, and facility audits in a GLP environment. Additionally, proficiency in HPLC, including the ability to assist scientists with HPLC-related questions and troubleshooting, is essential. You will also provide guidance and support to laboratory personnel, addressing regulatory and quality-related questions.
The successful candidate will have a strong understanding of 21 CFR Part 58 regulations and will be able to interpret and apply regulatory requirements effectively. Excellent communication and interpersonal skills are required to interact with lab personnel and cross-functional teams.
