At a Glance
- Tasks: Ensure compliance and certify batches for quality, safety, and efficacy in animal health manufacturing.
- Company: Join a global leader in animal health with a focus on innovation and quality.
- Benefits: Competitive salary, professional development, and a dynamic work environment.
- Why this job: Make a real impact in animal health while ensuring the highest standards of quality.
- Qualifications: Degree in a scientific discipline and experience as a Qualified Person.
- Other info: Collaborative team culture with opportunities for growth and leadership.
The predicted salary is between 50000 - 60000 £ per year.
A global animal health CDMO is seeking a Qualified Person to join its Dundee manufacturing site.
Overview
I'm working with a global animal-health specialist operating across contract research, development and manufacturing, supporting pharmaceutical companies from early development through to commercial supply.
The Role
As a Qualified Person, you will be named on the site licence and act in full compliance with the Veterinary Medicines Regulations (VMR) and Eudralex Volume 4, ensuring that all batches released meet the required standards of quality, safety and efficacy.
Key Responsibilities
- QP Certification & Compliance
- Certify batches prior to release in line with VMR, EU GMP, Annex 16, and relevant Marketing Authorisations.
- Ensure manufacturing and testing activities comply with authorised processes and validated systems.
- Review and assess production records, deviations, changes and investigations prior to certification.
- Ensure all required documentation, audits, tests and checks are completed and approved.
- Support ongoing compliance of the Quality Management System with legislative and regulatory requirements.
- Notify site leadership and customers of any issues impacting batch compliance.
- Maintain up-to-date knowledge of regulatory, scientific and quality management developments.
- Coordinate QP release activities across the QP team to support production and dispatch schedules.
- Act as Primary Deputy for the Site Quality Manager when required.
- Provide guidance and technical support on quality and compliance matters.
- Liaise directly with customers on quality-related topics.
About You
Qualifications
- Degree in a relevant scientific discipline as defined under the VMR, or chartered status.
- Member of the Royal Society of Chemistry, Biology or Pharmacy.
- Certificate of Eligibility to act as a Qualified Person (permanent provisions).
- Lead Auditor qualification (PR325 / PR330) - highly desirable.
Experience
- 3-5+ years' experience acting as a named QP on a manufacturing licence.
- Strong GMP background within pharmaceutical manufacturing.
- Veterinary medicinal product experience preferred, particularly:
- Non-sterile liquids.
- Suspensions.
Qualified Person in Scotland employer: ENTRUST PEOPLE LIMITED
Contact Detail:
ENTRUST PEOPLE LIMITED Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person in Scotland
✨Tip Number 1
Network like a pro! Reach out to industry professionals on LinkedIn or attend local events. We all know that sometimes it’s not just what you know, but who you know that can help you land that Qualified Person role.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of VMR and EU GMP regulations. We recommend practising common interview questions with a friend or in front of the mirror to boost your confidence.
✨Tip Number 3
Showcase your experience! When discussing your background, highlight specific projects where you ensured compliance or improved quality systems. We want to see how you’ve made an impact in previous roles.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Qualified Person in Scotland
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience and qualifications that match the role of a Qualified Person. We want to see how your background aligns with the Veterinary Medicines Regulations and GMP standards.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about animal health and how your skills can contribute to our team. Keep it concise but impactful, showing us your personality.
Showcase Your Compliance Knowledge: Since compliance is key in this role, make sure to mention any specific experiences you have with VMR, EU GMP, or quality management systems. We love seeing candidates who understand the importance of these regulations!
Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at ENTRUST PEOPLE LIMITED
✨Know Your Regulations
Make sure you brush up on the Veterinary Medicines Regulations (VMR) and Eudralex Volume 4. Being able to discuss these regulations confidently will show that you understand the compliance landscape and are ready to take on the responsibilities of a Qualified Person.
✨Showcase Your Experience
Prepare specific examples from your past roles where you successfully certified batches or handled compliance issues. Highlighting your 3-5+ years of experience as a named QP will help demonstrate your capability and readiness for the role.
✨Understand Quality Management Systems
Familiarise yourself with Quality Management Systems and how they relate to regulatory requirements. Be ready to discuss how you've supported compliance in previous positions, as this will be crucial for the role.
✨Engage with the Team
Since the role involves coordinating with the QP team and liaising with customers, practice your communication skills. Think about how you can convey technical information clearly and effectively, as well as how you can support your team in a fast-paced environment.