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- Tasks: Ensure quality standards for a new drug product facility and support compliance.
- Company: Ipsen, a leading pharmaceutical company focused on neuroscience therapies.
- Benefits: Exciting growth opportunities, competitive salary, and a collaborative work environment.
- Why this job: Join a dynamic team making a real impact in pharmaceutical manufacturing.
- Qualifications: Experience in pharma, strong GMP knowledge, and familiarity with sterile environments.
- Other info: Be part of a major expansion with excellent career development prospects.
The predicted salary is between 36000 - 60000 £ per year.
At Ipsen, we are committed to improving the lives of patients, with a special focus on advancing neuroscience therapies. Our Wrexham site is a vital part of this mission, delivering cutting‑edge solutions in a dynamic and collaborative environment. We are proud to be Great Place to Work certified and a Shingo Bronze Medallion holder, reflecting our commitment to excellence, innovation, and continuous improvement.
With a recent £24 million investment in the site and a further £86.4 million expansion underway, there has never been a more exciting time to join us. If you are passionate about making an impact and want to be part of a team that values growth, innovation, and excellence, then Ipsen could be where you thrive!
Want to get involved in the expansion? We’re looking for a QA Specialist to support the launch of a brand‑new drug product facility on our Wrexham manufacturing site. This facility is a major step forward in our pharmaceutical capabilities, and you’ll play a key role in bringing it online from a quality perspective. Your mission: ensure all documentation, processes, and systems meet GMP standards and are ready for operational excellence.
What You’ll Do
- Provide QA oversight for documentation and processes during the NDP facility set-up and beyond
- Support batch record review and ensure timely, compliant batch release.
- Lead investigations into deviations, OOS, CAPAs, and change controls.
- Deliver training and guidance on GMP and quality standards across teams.
- Represent QA in site projects and regulatory inspections.
- Drive continuous improvement and promote a proactive quality culture.
What We’re Looking For
- Experience in a similar role in pharma or biopharma.
- Strong knowledge of GMP, validation, and regulatory requirements.
- Experience in sterile manufacturing environments and batch release is highly preferred.
Apply now and be part of a milestone moment in pharmaceutical manufacturing at our Wrexham site.
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QA Specialist - New Facility employer: Ipsen
Contact Detail:
Ipsen Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA Specialist - New Facility
✨Tip Number 1
Network like a pro! Reach out to current employees at Ipsen on LinkedIn or other platforms. Ask them about their experiences and any tips they might have for landing the QA Specialist role. Personal connections can make a huge difference!
✨Tip Number 2
Prepare for the interview by brushing up on your GMP knowledge and relevant regulations. We recommend creating a list of potential questions you might be asked, especially around quality assurance processes. Being well-prepared shows your commitment to excellence!
✨Tip Number 3
Showcase your passion for continuous improvement! During interviews, share examples of how you've driven quality initiatives in past roles. This aligns perfectly with Ipsen's values and will help you stand out as a candidate who fits their culture.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re genuinely interested in being part of the Ipsen team and contributing to their exciting expansion.
We think you need these skills to ace QA Specialist - New Facility
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experience that match the QA Specialist role. Highlight your knowledge of GMP and any relevant experience in sterile manufacturing environments to catch our eye!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Share your passion for quality assurance and how you can contribute to our mission at Ipsen. Be sure to mention why you’re excited about the new facility and our commitment to excellence.
Showcase Your Achievements: Don’t just list your responsibilities; showcase your achievements! Use specific examples of how you’ve driven continuous improvement or handled quality challenges in previous roles. We love seeing how you’ve made an impact!
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 one step closer to joining our fantastic team at Ipsen!
How to prepare for a job interview at Ipsen
✨Know Your GMP Inside Out
Make sure you brush up on Good Manufacturing Practices (GMP) before your interview. Be ready to discuss how you've applied these standards in your previous roles, especially in sterile manufacturing environments. This will show that you understand the importance of compliance and quality assurance.
✨Showcase Your Problem-Solving Skills
Prepare examples of how you've led investigations into deviations or handled out-of-specification (OOS) results. Highlight your experience with CAPAs and change controls, as this will demonstrate your ability to drive continuous improvement and maintain operational excellence.
✨Emphasise Team Collaboration
Ipsen values a collaborative environment, so be ready to talk about how you've worked with cross-functional teams. Share specific instances where you delivered training or guidance on quality standards, showcasing your ability to foster a proactive quality culture.
✨Be Ready for Regulatory Questions
Since you'll be representing QA during regulatory inspections, it's crucial to prepare for questions related to compliance and documentation processes. Familiarise yourself with common regulatory requirements and be prepared to discuss how you've ensured adherence in past projects.
