What are the responsibilities and job description for the Quality Compliance Auditor position at The Fountain Group?
Currently I have an opening for a Quality Compliance Auditor located in Los Angeles, CA (Monterey Park Area). Details for the position are as follows :
Job Description :
- This position requires a strong background in pharmaceutical manufacturing and compliance, with a focus on routine GMP audits, technical audits, and managing license agreements.
- Conduct routine GMP audits as well as technical and special audits to ensure compliance with regulatory requirements.
- Manage license agreements, ensuring all terms are adhered to and any issues are addressed promptly.
- Provide expertise and leadership in pharma manufacturing compliance, ensuring alignment with cGXP standards and regulations.
- Lead and manage cross-functional projects, coordinating with teams across departments to ensure timely and successful audit outcomes.
- Review and assess manufacturing processes for adherence to industry regulations and internal policies.
- Prepare detailed audit reports, identifying potential non-compliance issues and recommending corrective actions.
- Maintain up-to-date knowledge of industry best practices, regulatory changes, and emerging trends in pharmaceutical manufacturing and compliance.
- The ideal candidate will have a bachelor’s degree and minimum of 5 years of experience in pharma / manufacturing environments, along with knowledge of cGXP regulations.
- Strong project management skills and experience leading cross-functional teams are also key for success in this role.
Technical Information :
Salary : $53 - $61
