At a Glance
- Tasks: Lead quality assurance for clinical studies and ensure compliance with regulations.
- Company: Ipsen, a global biopharmaceutical company focused on transformative medicines.
- Benefits: Competitive salary, inclusive culture, and opportunities for professional growth.
- Other info: Dynamic global environment with a commitment to inclusion and personal growth.
- Why this job: Join a passionate team making a real impact on patient safety and clinical quality.
- Qualifications: Experience in pharmaceutical quality assurance and strong collaboration skills required.
The predicted salary is between 59400 - 72600 £ per year.
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 endeavour 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!
About the Role: Join our Global Quality organisation as a Manager, QA Operations, supporting Clinical & Medical Quality Assurance. In this role, you’ll work closely with R&D and Global Medical Affairs teams to help ensure clinical studies and programmes are conducted in line with Good Clinical Practice, regulatory requirements and Ipsen quality standards. You’ll provide hands-on Quality Assurance expertise and guidance to cross-functional study teams, supporting quality oversight throughout the clinical lifecycle. This is a great opportunity for someone with established pharmaceutical Quality experience who is ready to broaden their experience across clinical studies, quality systems and compliance activities in a global environment.
Key Responsibilities:
- Provide quality 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
What We’re Looking For:
- Established pharmaceutical industry experience, with a strong background in Quality supporting Medical Affairs and/or R&D
- Experience working with interventional and/or non-interventional clinical studies
- Good working knowledge of Good Clinical Practice (GCP) and relevant clinical quality requirements
- Strong collaboration, communication and problem-solving skills, with the ability to work effectively across functions in a global environment
- A master’s degree or higher in a relevant scientific or life sciences discipline, with fluent English
Why Join Us?
Be part of a global Quality team where you can build your Clinical QA expertise, work with cross-functional teams and make a meaningful contribution to clinical quality and patient safety. Ready to take the next step in your Clinical Quality career? Apply today and help us continue to strengthen quality across our clinical and medical activities.
Manager, QA operations in London employer: Ipsen
Ipsen Biopharm Ltd is an exceptional employer that prioritises a human-centric workplace culture, fostering collaboration and excellence. With a commitment to employee growth, Ipsen offers opportunities for continuous improvement and innovation in the biopharmaceutical field, particularly in vibrant locations like Paris and London. Employees are empowered to thrive, making a meaningful impact on patients and society while enjoying a supportive environment that values diverse perspectives.
StudySmarter Expert Advice🤫
We think this is how you could land Manager, QA operations in London
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Ipsen. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Ipsen.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Ipsen. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Ipsen is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Manager, QA operations in London
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Ipsen!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Ipsen that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Ipsen!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Ipsen, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Ipsen
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Ipsen that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Ipsen’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
