Global QA Operations Manager, Clinical & Medical

Ipsen Innovation (SAS); Paris; On-site; EUR 90,000 - 120,000; Full time

Job summary

Ipsen Innovation (SAS) seeks a Manager, QA Operations to lead quality oversight for clinical studies and programmes in line with GCP and Ipsen quality standards. The role collaborates with R&D, Medical Affairs and cross-functional teams to ensure compliant, high-quality clinical activities across global programs.

Ideal candidates will have established pharmaceutical QA experience supporting Medical Affairs and/or R&D, with strong GCP knowledge and fluent English.

Qualifications

• Pharmaceutical industry experience with QA supporting Medical Affairs and/or R&D.
• Experience with interventional and/or non-interventional clinical studies.
• Strong knowledge of Good Clinical Practice (GCP) and clinical quality requirements.
• Excellent collaboration and communication across global teams.
• Master’s degree or higher in life sciences with fluent English.

Responsibilities

• Provide QA oversight for assigned clinical studies and programmes, ensuring alignment with GCP, regulatory requirements and internal quality standards.
• Partner with clinical and medical teams, providing practical QA expertise and guidance.
• Identify and manage quality risks, including Quality Events, investigations, CAPAs and potential serious GCP breaches.
• Support inspection readiness, GCP inspections, quality assessments and audit activities.
• Support risk-based quality oversight of clinical service providers.
• Contribute to the development and continuous improvement of the Clinical & Medical Quality Management System.

Skills

QA Operations

GCP knowledge

Cross-functional collaboration

Quality oversight

Education

Master's degree in life sciences

Job description

Ipsen Innovation (SAS) seeks a Manager, QA Operations to lead quality oversight for clinical studies and programmes in line with GCP and Ipsen quality standards. The role collaborates with R&D, Medical Affairs and cross-functional teams to ensure compliant, high-quality clinical activities across global programs.

Ideal candidates will have established pharmaceutical QA experience supporting Medical Affairs and/or R&D, with strong GCP knowledge and fluent English.