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- Tasks: Join as a Qualified Person to certify and release medicinal products.
- Company: Be part of a growing pharmaceutical company with a strong pipeline.
- Benefits: Enjoy a supportive, flexible work environment focused on quality and compliance.
- Why this job: Make a real impact in a specialist setting with high visibility and leadership opportunities.
- Qualifications: Must be eligible to act as a QP in the UK with significant GMP experience.
- Other info: Collaborate with various functions and participate in audits for continuous improvement.
The predicted salary is between 36000 - 60000 £ per year.
Job Description
We are supporting a growing pharmaceutical company with a strong pipeline and established manufacturing operations, as they look to appoint a Qualified Person (QP) to join their Quality and Supply organisation. This is a permanent role offering long-term impact, high visibility, and an opportunity to contribute to both commercial and clinical product release in a specialist setting.
Key Responsibilities:
- Act as a named QP for the certification and release of licensed and investigational medicinal products
- Ensure all batches meet regulatory, GMP, and internal quality requirements prior to release
- Work closely with Quality Assurance, Manufacturing, Regulatory Affairs, and Supply Chain functions
- Participate in internal and external audits, including those by regulatory authorities
- Support continuous improvement of quality systems and manufacturing processes
- Provide expert guidance on GMP compliance and regulatory expectations across the site
Candidate Requirements:
- Eligible to act as a QP in the UK
- Significant GMP experience within pharmaceutical manufacturing, ideally across both clinical and commercial environments
- Excellent knowledge of quality systems, regulatory frameworks, and pharmaceutical supply chain requirements
- Strong communication skills and a collaborative working style
- Ability to operate effectively in a high-standard, fast-paced environment
What the Role Offers:
- The opportunity to play a key leadership role within a specialist pharmaceutical organisation
- Visibility across manufacturing, quality, and regulatory functions
- A supportive, flexible working environment with a strong focus on quality and compliance
Qualified Person employer: Nexia
Contact Detail:
Nexia Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who are already working as Qualified Persons. Attend industry conferences or seminars to make connections and learn about potential job openings.
✨Tip Number 2
Stay updated on the latest regulatory changes and GMP guidelines relevant to the pharmaceutical sector. This knowledge will not only enhance your expertise but also demonstrate your commitment to quality and compliance during interviews.
✨Tip Number 3
Prepare for potential interview questions by reviewing common scenarios a QP might face, such as handling non-compliance issues or leading audits. Practising your responses can help you articulate your experience and problem-solving skills effectively.
✨Tip Number 4
Showcase your collaborative working style by discussing past experiences where you successfully worked with cross-functional teams. Highlighting your ability to communicate and cooperate with various departments will be crucial in this role.
We think you need these skills to ace Qualified Person
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Qualified Person. Familiarise yourself with the key requirements and expectations outlined in the job description.
Tailor Your CV: Highlight your relevant experience in GMP and pharmaceutical manufacturing. Make sure to emphasise any roles where you've acted as a QP or have been involved in quality assurance processes.
Craft a Compelling Cover Letter: Use your cover letter to showcase your passion for quality and compliance in the pharmaceutical industry. Mention specific examples of how you've contributed to quality systems and regulatory compliance in previous roles.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter. Look for any spelling or grammatical errors, and ensure that your documents are clear and professional.
How to prepare for a job interview at Nexia
✨Showcase Your GMP Experience
Make sure to highlight your significant GMP experience during the interview. Be prepared to discuss specific examples from your past roles that demonstrate your understanding of Good Manufacturing Practices and how you've applied them in both clinical and commercial settings.
✨Understand Regulatory Frameworks
Familiarise yourself with the relevant regulatory frameworks that govern pharmaceutical manufacturing. Being able to discuss these regulations confidently will show your potential employer that you are well-versed in compliance and can navigate the complexities of the industry.
✨Emphasise Collaboration Skills
Since the role requires working closely with various departments, emphasise your strong communication skills and collaborative working style. Prepare examples of how you've successfully worked with Quality Assurance, Manufacturing, and Regulatory Affairs teams in the past.
✨Prepare for Audits Discussion
Be ready to discuss your experience with internal and external audits, including those by regulatory authorities. Share specific instances where you contributed to audit preparations or responses, showcasing your ability to maintain high standards in a fast-paced environment.
