Clinical Vendor QA Senior Specialist

Title:

Clinical Vendor QA Senior Specialist

Company:

Ipsen Biopharm Ltd

 

About Ipsen:

Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation.

 Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society!

For more information, visit us at https://www.ipsen.com/ and follow our latest news on LinkedIn and Instagram.

Job Description:

About the Role

Join our Global Quality organization as a key contributor to Clinical & Medical QA. Within QA Operations, you will ensure quality oversight of service providers involved in clinical studies and programs. You’ll develop and maintain effective quality systems, ensure compliance with internal and external standards, and act as a partner to Clinical Trial Excellence and Procurement.

Key Responsibilities

• Oversee qualification and ongoing quality oversight of service providers

• Lead service provider quality oversight meetings and ensure follow-up on actions

• Monitor and report on service provider quality performance

• Maintain quality agreements and ensure alignment with contracts

• Support audit and inspection readiness, including CAPA implementation

• Contribute to training and continuous improvement initiatives

What We’re Looking For

• Demonstrated experience in the pharmaceutical industry, with a solid background in quality roles supporting medical affairs or R&D

• Experience in quality oversight of service providers within pharma

• Experience in interventional/non-interventional clinical studies

• Master’s degree or higher in a relevant scientific discipline (preferred: Master’s in quality or PhD)

• Fluent English required

• Strong skills in collaboration, problem-solving, and driving results

Why Join Us?

• Collaborative Work Environment: Work with dynamic, globally connected teams and cross-functional partners in R\&D, Medical Affairs, Procurement, and Legal.

• Career Growth & Impact: Opportunities to lead or co-lead global projects, clear pathways for career progression, and the chance to make a real impact on patient safety and compliance.

• Recognition & Development: Global recognition programs, ongoing feedback, annual performance reviews, and access to learning and professional development opportunities.

Ready to drive quality excellence? Apply today and be part of a company that values your growth, wellbeing, and impact!

#LI-Hybrid

We are committed to creating a workplace where everyone feels heard, valued, and supported; where we embrace “The Real Us”. The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities. When we include diverse ways of thinking, we make more thoughtful decisions and discover more innovative solutions. Together we strive to better understand the communities we serve. This means we also want to help you perform at your best when applying for a role with us. If you require any adjustments or support during the application process, please let the recruitment team know. This information will be handled with care and will not affect the outcome of your application.