What are the responsibilities and job description for the Quality Compliance Auditor position at Rishabh RPO?
Job Description
Job Description
Job Title : Quality / Compliance Auditor
Location- 5555 Valley Blvd, Los Angeles, CA 90032
Start Date : 02 / 17 / 2025 End Date 02 / 22 / 2026 (Possible extension for longer term)
Summary :
This position entails performing routine GMP audits as well as specialty and technical audits in relation to current products and prospective in-license agreements, providing compliance guidance and support throughout the Quality organization, training delivery, and leading multi-departmental teams and initiatives.
To ensure success as a Quality Auditor, the candidate should possess in-depth knowledge of product standards and extensive pharmaceutical experience preferably in manufacturing, quality assurance, and / or cGxP auditing and demonstrated project management experience in leading cross-functional teams.
Key Responsibilities :
- To ensure success as a Quality Auditor, the candidate should possess in-depth knowledge of product standards and extensive experience as a related pharmaceutical experience preferably in manufacturing, quality assurance, or cGxP auditing and demonstrated project management experience in leading cross-functional teams.
- Prepare and execute internal self-inspections and supplier audits and issue reports. Follow up on post audit action tracking & progress.
- Assisting in implementing Internal Audit plans for all manufacturing plants.
- Assisting in implementing Supplier Audit plans for all manufacturing plants.
- Trends, analyses, and reports on quality data to improve product and process Quality for all plants; develop actions for improvement based on data analyses. Peer Review of Audits Reports.
- Provide support prior, during and post inspections for external Regulatory Inspections, Customer Audits and Corporate Internal Audits.
- Ensures the corrections of findings, risks and improvements are promptly and thoroughly incorporated into the quality systems.
- Keeping abreast of industry standards and regulations.
- All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional task and responsibilities.
- Contribution to the continuous improvement of the Quality Management System is required.
- Other additional duties may be assigned by the Director Quality Audits from time to time if required.
- Ability to travel (up to 30%)
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Qualifications :
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