At a Glance
- Tasks: Ensure compliance and quality in animal health manufacturing as a Qualified Person.
- Company: Global leader in animal health with a strong mission and values.
- Benefits: Competitive salary, flexible pay based on experience, and growth opportunities.
- Other info: Join a well-invested site in Dundee with a dynamic team.
- Why this job: Make a real impact in animal health with high visibility and influence.
- Qualifications: Degree in relevant science, QP certification, and 3-5 years of experience.
The predicted salary is between 55000 - 85000 £ per year.
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.
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- 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
- Perform external audits where required
- Liaise directly with customers on quality-related topics
- 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
- 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
- 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 in Portsmouth 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. Experience a rewarding career that not only supports your professional development but also contributes to the health and wellbeing of animals worldwide.
Contact Details:
Entrust Resource Solutions Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Qualified Person in Portsmouth
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We think you need these skills to ace Qualified Person in Portsmouth
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 Entrust Resource Solutions!
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 Entrust Resource Solutions 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 Entrust Resource Solutions!
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 Entrust Resource Solutions, 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 Entrust Resource Solutions
✨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 Entrust Resource Solutions 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 Entrust Resource Solutions’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.
