Quality Analyst III – External Manufacturing

About the role

As a Quality Analyst you will join Teva External Manufacturing (ExM) Quality – Central Services, preparing and reviewing QMS documents such as SOPs, risk maps and CAPAs to ensure compliance with Teva’s Quality Management System.

Key responsibilities

• Create and maintain standard operating procedures in line with Teva standards and applicable legislation.
• Translate SOPs into training assignments, curricula, quizzes and training records while maintaining GMP compliance.
• Perform gap assessments on SOPs against new or revised Teva standards.
• Support inspection readiness by reviewing checklists and coordinating with suppliers for additional evidence.
• Prepare and monitor self‑inspection schedules and conduct inspections as required.

Required profile

• Master’s degree in Pharmaceutical/Life Sciences or a related field.
• 5+ years of experience in quality control, production, or quality assurance.
• Working knowledge of cGMPs and relevant international regulations/guidelines.
• Strong written and spoken English communication skills.

Required skills

• MS Office
• Veeva

What we offer

• Dynamic and challenging work environment in a leading pharmaceutical company.
• Competitive remuneration linked to performance.
• Additional healthcare insurance.
• Transportation allowance and flexible benefits.
• Option to work from home according to company policy.
• Opportunities for professional development.