At a Glance
- Tasks: Ensure compliance with veterinary regulations and certify pharmaceutical batches for quality and safety.
- Company: Global animal-health specialist with a strong mission and values.
- Benefits: Competitive salary, flexible options, and a dynamic work environment.
- Other info: Join a growing team at a well-invested manufacturing site in Dundee.
- Why this job: Make a real impact in animal health while working in a high-visibility role.
- Qualifications: Degree in a relevant scientific discipline and experience as a Qualified Person.
The predicted salary is between 100000 - 100000 £ per year.
The Opportunity
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.
This organisation is purpose-driven, operating exclusively within animal health, and partners with customers across pet, livestock and veterinary medicines. With a strong international footprint and continued site investment in the UK, they are now strengthening their Qualified Person (QP) capability at their Dundee manufacturing facility.
This is a high-impact QP role with genuine visibility across site leadership, customers and regulatory stakeholders.
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.
You will play a key role in batch certification, QMS oversight, and wider site quality leadership, working closely with operations, quality, regulatory and client teams.
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
Quality System Oversight
- 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
Site Team Leadership
- 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
- Perform external audits where required
- 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
- Confident operating in a customer-facing, fast-paced manufacturing environment
Why This Role?
- Join a global animal-health specialist with a clear mission and strong values
- High-visibility QP position with real influence across site and customers
- Competitive salary range with flexibility for the right experience
- Dundee-based role within a growing and well-invested manufacturing site
Qualified Person - Pharmaceuticals employer: Entrust Resource Solutions
Join a purpose-driven global animal-health specialist in Dundee, where you will have the opportunity to make a significant impact as a Qualified Person. With a strong commitment to employee growth and a collaborative work culture, this organisation offers competitive salaries, ongoing training, and the chance to work closely with site leadership and regulatory stakeholders in a well-invested manufacturing environment.
Contact Details:
Entrust Resource Solutions Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Qualified Person - Pharmaceuticals
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical and animal health sectors. Attend industry events or webinars, and don’t be shy about introducing yourself. You never know who might have the inside scoop on job openings!
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of Veterinary Medicines Regulations and EU GMP standards. Be ready to discuss how your experience aligns with the role of a Qualified Person. Show them you’re not just a fit on paper but also in practice!
✨Tip Number 3
Don’t forget to leverage social media! Follow companies you’re interested in, engage with their posts, and share relevant content. This can help you get noticed and show your passion for the industry.
✨Tip Number 4
Apply through our website for the best chance at landing that dream job! We make it easy for you to showcase your skills and experience directly to employers looking for qualified candidates like you.
We think you need these skills to ace Qualified Person - Pharmaceuticals
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Qualified Person role. Highlight your experience with GMP and any relevant qualifications, like your degree and QP certification. We want to see how your background aligns with our mission in animal health!
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 – we love a good story!
Showcase Relevant Experience:When detailing your experience, focus on your time as a named QP and any specific projects that demonstrate your compliance with VMR and EU GMP. We’re looking for examples that show your leadership and quality oversight skills.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us you’re keen on joining our purpose-driven team!
How to prepare for a job interview at Entrust Resource Solutions
✨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’re not just familiar with them, but that you can apply them in a practical setting.
✨Showcase Your Experience
Prepare specific examples from your past roles where you’ve successfully certified batches or overseen quality management systems. Highlighting your hands-on experience with GMP and veterinary medicinal products will set you apart from other candidates.
✨Demonstrate Leadership Skills
Since this role involves site team leadership, be ready to discuss how you've coordinated teams or led projects in the past. Share instances where your guidance made a difference in compliance or quality outcomes.
✨Engage with Questions
Prepare thoughtful questions about the company’s approach to quality assurance and their future plans in animal health. This shows your genuine interest in the role and helps you assess if the company aligns with your values.
