Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Ensure quality oversight of service providers in clinical studies and maintain effective quality systems.
- Company: Join a global leader in the pharmaceutical industry focused on quality and patient safety.
- Benefits: Full-time role with career growth, recognition programs, and professional development opportunities.
- Why this job: Make a real impact on patient safety while collaborating with dynamic, cross-functional teams.
- Qualifications: Experience in pharma quality roles and a Master's degree in a relevant scientific discipline preferred.
- Other info: Be part of a supportive environment that values your growth and wellbeing.
The predicted salary is between 36000 - 60000 £ per year.
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
Qualifications
- 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
- 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.
Prepare to drive quality excellence. Apply today and be part of a company that values your growth, wellbeing, and impact!
Clinical Vendor QA Senior Specialist employer: Ipsen
Contact Detail:
Ipsen Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Vendor QA Senior Specialist
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work in QA or clinical roles. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of quality oversight and compliance standards. We recommend practising common interview questions related to service provider management and CAPA implementation to show you’re ready to hit the ground running.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a quick thank-you email to express your appreciation and reiterate your interest in the role. It keeps you fresh in their minds and shows your enthusiasm.
✨Tip Number 4
Apply through our website for the best chance at landing that Clinical Vendor QA Senior Specialist role. We love seeing candidates who take the initiative to engage directly with us, and it helps streamline the process!
We think you need these skills to ace Clinical Vendor QA Senior Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Vendor QA Senior Specialist role. Highlight your experience in quality oversight and any relevant qualifications that align with the job description. We want to see how your background fits into our team!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance in the pharmaceutical industry and how you can contribute to our mission at Ipsen. Keep it engaging and personal – we love to see your personality!
Showcase Your Skills: Don’t forget to highlight your collaboration, problem-solving, and results-driven skills in your application. These are key traits we value at StudySmarter, and demonstrating them will help us see how you can thrive in our collaborative environment.
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to keep track of your application status. Plus, we love seeing candidates who take the initiative!
How to prepare for a job interview at Ipsen
✨Know Your Quality Standards
Make sure you’re well-versed in the quality standards relevant to the pharmaceutical industry. Brush up on both internal and external compliance requirements, as this will show your potential employer that you understand the importance of maintaining high-quality oversight.
✨Showcase Your Collaboration Skills
Since the role involves working with cross-functional teams, be prepared to discuss examples of how you've successfully collaborated in the past. Highlight specific instances where your problem-solving skills led to positive outcomes in a team setting.
✨Prepare for Quality Oversight Scenarios
Think about potential scenarios related to service provider quality oversight that could come up during the interview. Prepare to discuss how you would handle these situations, including monitoring performance and ensuring compliance with quality agreements.
✨Demonstrate Continuous Improvement Mindset
Be ready to talk about your experience with training and continuous improvement initiatives. Share examples of how you've contributed to enhancing quality systems or processes, as this aligns perfectly with the expectations of the role.
