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- Tasks: Certify and release innovative medicinal products while ensuring compliance with quality standards.
- Company: Leading pharmaceutical manufacturer focused on quality, collaboration, and innovation.
- Benefits: Competitive salary, generous leave, private medical and dental insurance, and flexible working options.
- Why this job: Join a dynamic team shaping the future of safe, sustainable medicines globally.
- Qualifications: Registered Qualified Person with a degree in a relevant scientific discipline and cGMP knowledge.
- Other info: Supportive environment with excellent career growth and wellbeing programmes.
The predicted salary is between 80000 - 100000 £ per year.
ARx Recruitment Services are supporting a leading pharmaceutical manufacturing organisation in the search for a Qualified Person (QP) to join their quality leadership team at a modern manufacturing facility in the North West of the UK. This is an exciting opportunity to play a key role in the release of innovative medicinal products while helping shape quality strategy across a growing organisation focused on delivering safe, sustainable medicines to global markets. The role offers a competitive salary of £80,000 – £100,000, a discretionary bonus, and a comprehensive benefits package.
As a Qualified Person (QP) you will hold responsibility for the certification and release of both commercial and investigational medicinal products, ensuring full compliance with regulatory and GMP requirements. This is a senior position within the Quality function where you will contribute to quality culture, regulatory compliance, and lifecycle management of pharmaceutical products, while supporting innovation across manufacturing and development activities.
Key Responsibilities- Certify and release medicinal product batches in accordance with UK legislation and EU GMP
- Ensure compliance with regulatory requirements and quality standards
- Provide QP oversight across commercial and investigational product manufacturing
- Support regulatory inspections and audits, including interaction with regulatory authorities
- Influence and strengthen quality culture across operational teams
- Provide strategic input into quality systems, compliance, and continuous improvement initiatives
- Support new product introduction, validation, and lifecycle management activities
- Registered Qualified Person (QP) under current UK legislation
- Degree in a relevant scientific discipline
- Strong knowledge of current Good Manufacturing Practice (cGMP)
- Significant experience within pharmaceutical manufacturing environments
- Proven experience supporting regulatory inspections and audits
- Ability to influence quality behaviours across cross-functional teams
- Experience across multiple dosage forms and product lifecycle stages (desirable)
- 25 days annual leave plus bank holidays
- Discretionary bonus
- Generous employer pension contribution
- Private medical insurance
- Private dental insurance
- Permanent health insurance
- Group life assurance
- Wellbeing programmes and recognition schemes
- Free onsite parking
- Additional employee benefits and flexible working arrangements
This position offers the chance to join an organisation that values quality, collaboration, and innovation. You will work alongside experienced professionals in a supportive environment where compliance, sustainability, and continuous improvement are central to the company’s mission.
If you are an experienced Qualified Person seeking a new challenge in pharmaceutical manufacturing, we would be pleased to hear from you. Apply today or contact ARx Recruitment Services for a confidential discussion.
Qualified Person in Chester employer: ARx Recruitment Services
Contact Detail:
ARx Recruitment Services Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person in Chester
✨Network Like a Pro
Get out there and connect with people in the pharmaceutical industry! Attend events, join online forums, and don’t be shy about reaching out to professionals on LinkedIn. 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.
✨Show Off Your Skills
When you get the chance to chat with potential employers, make sure to highlight your experience with regulatory inspections and audits. We want to see how you can influence quality behaviours and contribute to a strong quality culture. Be ready to share specific examples of your past successes!
✨Prepare for the Interview
Do your homework on the company and its products before the interview. We recommend brushing up on current Good Manufacturing Practice (cGMP) and any recent developments in the pharmaceutical sector. This will show your genuine interest and help you stand out as a knowledgeable candidate.
✨Apply Through Our Website
Don’t forget to apply through our website for the best chance at landing that dream job! We make it easy for you to submit your application and keep track of your progress. Plus, we’re always here to support you throughout the process!
We think you need these skills to ace Qualified Person in Chester
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Qualified Person role. Highlight your experience with regulatory compliance and GMP, as well as any relevant qualifications. We want to see how your background aligns with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality in pharmaceutical manufacturing and how you can contribute to our mission. Keep it concise but impactful – we love a good story!
Showcase Your Achievements: Don’t just list your responsibilities; showcase your achievements! Use specific examples of how you've influenced quality culture or supported regulatory inspections. We’re keen to see how you’ve made a difference in your previous roles.
Apply Through Our Website: We encourage you to apply 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. Plus, it’s super easy!
How to prepare for a job interview at ARx Recruitment Services
✨Know Your Regulations
Make sure you brush up on UK legislation and EU GMP requirements before the interview. Being able to discuss specific regulations and how they apply to the role will show that you're not just familiar with the basics, but that you truly understand the compliance landscape.
✨Showcase Your Experience
Prepare to share concrete examples from your past roles where you've successfully certified and released medicinal products. Highlight any experiences with regulatory inspections and audits, as this will demonstrate your hands-on knowledge and ability to navigate complex situations.
✨Emphasise Quality Culture
Be ready to talk about how you've influenced quality behaviours in previous positions. Discuss strategies you've implemented to strengthen quality culture within teams, as this aligns perfectly with the company's focus on collaboration and continuous improvement.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's quality strategy and how they support innovation in manufacturing. This shows your genuine interest in the role and helps you gauge if the company’s values align with yours.