Quality​/Compliance Auditor

Description: Job Title:
Quality / Compliance Auditor
Pay Rate:
Starting at $30 / hr (DOE)

Location:

Los Angeles, CA
Area Code: 213, 310, 323, 424, 747, and 818
ZIP Code: 90032

Start Date:

Right Away
Keywords: #Quality Auditor #GMPJobs #Manufacturing Jobs

• Medical / Health Benefits with multiple plan options, Flexible Spending Accounts, Dental and Vision
• 401k
• On the job training / cross-training
• Life Insurance, disability insurance, and voluntary life insurance for family members available.
• Accident and critical illness insurance optional.
• Scheduled performance reviews
• Referral program

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.

• 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.
• Ensure the corrections of findings, risks and improvements are promptly and thoroughly incorporated into the quality systems.
• Keeping abreast of industry standards and regulations.
• Contribution to the continuous improvement of the Quality Management System.
• Work and grow in a team‑oriented environment and continue to build synergies between the Quality Audits group and internal and external quality and manufacturing groups.
• Other additional duties may be assigned.

• Bachelor's degree in a scientific discipline.
• 5+ years related pharmaceutical experience, preferably in manufacturing, quality assurance, or cGxP auditing.
• Demonstrated project management experience in leading cross‑functional teams.
• ASQ Certification as a Quality Auditor, Manager, or Engineer a plus.
• Superior knowledge of U.S. cGMPs and FDA guidance.
• Experience in SAP is preferred.

• Strong interpersonal skills.
• Excellent written and verbal communication skills.
• Effective influence management and conflict resolution abilities.
• Highly developed investigative and reporting skills.
• Effective organization and time management skills.
• Ability to travel (up to 30%).
• Ability to generate and/or maintain reports, databases and presentations using Microsoft Office.
• Flexible, able to adapt quickly to change in a fast‑paced environment.
• In‑depth knowledge of product standard.

Belcan is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.

• Beneficios médicos/de salud con múltiples opciones de planes, cuentas de gastos flexibles, seguro dental y de la vista
• 401k
• Capacitación en el trabajo/capacitación cruzada
• Seguro de vida, seguro por discapacidad y seguro de vida voluntario para miembros de la familia disponibles.
• Seguro por accidente y enfermedad grave opcional.
• Revisiones de desempeño programadas
• Programa de referencias

Realizar auditorías de rutina de GMP, así como auditorías técnicas y especializadas en relación con los productos actuales y los posibles acuerdos de licencia, brindar orientación y apoyo de cumplimiento en toda la organización de calidad, brindar capacitación y liderar equipos e iniciativas multidepartamentales.

• Preparar y ejecutar autoinspecciones internas y auditorías de proveedores y emitir informes.
• Realizar un seguimiento y progreso de las acciones posteriores a la auditoría.
• Ay…