Quality Assurance Auditor

About the role

Join Teva, a leading biopharmaceutical company, as a Quality Assurance Auditor. You will be responsible for overseeing internal, external, and supplier audit programs to ensure compliance with GMP regulations and corporate quality standards.

Key responsibilities

• Lead and manage the site’s audit programs, covering internal, external, and supplier audits.
• Develop, coordinate, and monitor the annual audit plan, organize cross‑functional audit teams, and follow up on corrective and preventive actions (CAPAs).
• Drive continuous‑improvement initiatives by assessing cGMP compliance, identifying risks, and partnering with functional teams to implement corrective actions.
• Maintain audit readiness through effective audit systems, procedures, and inspection‑preparedness programs.
• Conduct supplier and third‑party audits to verify GMP compliance and adherence to quality agreements.
• Prepare and update audit‑related procedures in line with corporate policies and global regulatory requirements.
• Support Regulatory Affairs and regional quality teams with audit documentation and compliance data for product registrations.
• Monitor and report quality compliance metrics and KPIs, fostering a culture of quality and continuous improvement.

Required profile

• Bachelor’s degree in Pharmacy, Chemistry, Biochemistry, Engineering, or a related scientific/technical discipline.
• 3‑5 years of experience in the pharmaceutical industry or other regulated manufacturing environments.
• Experience in Quality Assurance, Quality Control, Manufacturing, or Quality Systems, including process controls and documentation management.
• Strong knowledge of GMP/cGMP requirements and pharmaceutical quality systems.
• Understanding of pharmaceutical regulations and health‑authority standards, including ANMAT and international regulations.
• Proven experience performing audits, assessing compliance risks, and managing corrective actions.

Required skills

• GMP/cGMP compliance
• Audit management and execution
• Process control documentation
• Regulatory standards knowledge (ANMAT, international)

What we offer

• Opportunity to work in a high‑performing, inclusive culture.
• Professional growth and development within a global biopharmaceutical leader.
• Flexibility to balance life and work while contributing to worldwide health improvement.