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:

• Pay: $53-61 hourly, depending on experience level
• Onsite, M-F, 8am-4:30pm, occasional travel to local sites
• 12-month contract, potential for extension or conversion