Quality Auditor Full Time

Title – Quality Auditor/QA Specialist

Months- 12+ Months (potential extension)

Location- Los Angeles, CA

Pay Range- $50-60/hr. on W2

Job Description

Summary:

The Quality / Compliance Auditor will conduct routine GMP audits, specialty audits, and technical audits related to current products and prospective in-license agreements. The role also involves providing compliance guidance, delivering training, and leading multi-departmental teams and initiatives.

A successful candidate will have extensive pharmaceutical experience, particularly in manufacturing, quality assurance, and/or cGxP auditing, along with strong project management capabilities in leading cross-functional teams.

Key Responsibilities:

• Conduct internal self-inspections and supplier audits, preparing and issuing detailed reports.
• Track and monitor post-audit action plans and progress.
• Support the implementation of Internal Audit plans across all manufacturing plants.
• Assist in executing Supplier Audit plans for manufacturing sites.
• Analyze and report quality data trends to enhance product and process quality across plants.
• Conduct peer reviews of audit reports.
• Provide support before, during, and after external regulatory inspections, customer audits, and corporate internal audits.
• Ensure corrective actions, risk mitigations, and process improvements are effectively integrated into the quality management system.
• Stay updated on evolving industry standards and regulatory requirements.
• Contribute to the continuous improvement of the Quality Management System.
• Perform additional tasks as assigned by the Director of Quality Audits.
• Travel up to 30% as required.

Skills & Abilities:

Skills:

• Strong interpersonal and communication skills (written and verbal).
• Effective influence management and conflict resolution abilities.
• Strong investigative and reporting skills.
• Excellent organization and time management.
• Ability to work in a team-oriented environment and foster collaboration between quality audits, manufacturing, and quality assurance groups.

Abilities:

• Willingness to travel (up to 30%).
• Proficiency in Microsoft Office for report generation, database management, and presentations.
• Adaptability to a fast-paced environment with evolving priorities.

Qualifications:

• Education: Minimum Bachelor’s degree in a scientific discipline.
• Experience: Minimum 5+ years of related pharmaceutical experience, preferably in manufacturing, quality assurance, or cGxP auditing.
• Certifications: ASQ Certification as a Quality Auditor, Manager, or Engineer is a plus.
• Regulatory Knowledge: Strong understanding of U.S. cGMPs and FDA guidance.
• Desirable Experience: Proficiency in SAP.

Dexian is a leading provider of staffing, IT, and workforce solutions with over 12,000 employees and 70 locations worldwide. As one of the largest IT staffing companies and the 2nd largest minority-owned staffing company in the U.S., Dexian was formed in 2023 through the merger of DISYS and Signature Consultants. Combining the best elements of its core companies, Dexian’s platform connects talent, technology, and organizations to produce game-changing results that help everyone achieve their ambitions and goals.

Dexian’s brands include Dexian DISYS, Dexian Signature Consultants, Dexian Government Solutions, Dexian Talent Development and Dexian IT Solutions. Visit

to learn more.

Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status

Tagged as: Manufacturing