Quality Compliance Specialist (cGXP & Data Integrity)

Teva Pharmaceuticals; Amsterdam; On-site; EUR 60,000 - 90,000; Full time

Job summary

Teva Pharmaceuticals in Amsterdam is seeking a Quality Compliance Associate to support the site's Quality Systems & Compliance team, ensuring cGXP adherence and robust data integrity across processes. You will manage vendor qualifications and assist in inspection readiness within a multinational pharma setting.

The role requires a strong background in pharmaceutical quality, with cross-functional collaboration across departments, and fluency in English; Dutch is a plus.

Qualifications

• University degree in Pharmacy, Chemistry, or related field, or HBO+ with quality industry experience.
• Proven experience with pharmaceutical processes, quality systems, and cGXP requirements.
• Familiarity with process automation in regulated environments; strong data integrity knowledge.
• Ability to translate SOPs and quality requirements into day-to-day operations.
• Experience supporting inspections and audits; cross-functional teamwork.

Responsibilities

• Prepare and support department policies aligned with Teva and site policies.
• Coordinate and implement Teva standards and procedures at the site.
• Ensure compliance with national and international cGXP quality standards.
• Organize vendor evaluation and maintain their qualification status.
• Support inspection preparation and front/back office during inspections.
• Use analyses to identify root causes and determine CAPAs.
• Ensure Data Integrity awareness and lead Data Integrity projects.
• Maintain permanent inspection readiness across the site.

Skills

Quality systems

cGXP compliance

Data integrity

Vendor qualification

Inspection readiness

Cross-functional teamwork

English fluency

Education

University degree in Pharmacy

HBO+ level qualification

Tools

QMS software

Regulatory databases

Job description

Teva Pharmaceuticals in Amsterdam is seeking a Quality Compliance Associate to support the site's Quality Systems & Compliance team, ensuring cGXP adherence and robust data integrity across processes. You will manage vendor qualifications and assist in inspection readiness within a multinational pharma setting.

The role requires a strong background in pharmaceutical quality, with cross-functional collaboration across departments, and fluency in English; Dutch is a plus.