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- Tasks: Join our team as a Qualified Person, ensuring product quality and compliance.
- Company: Be part of a growing pharmaceutical company with a strong pipeline and established operations.
- Benefits: Enjoy a supportive, flexible work environment with opportunities for professional growth.
- Why this job: Make a real impact in a specialist setting while collaborating with diverse teams.
- Qualifications: Must have significant GMP experience and be eligible to act as a QP in the UK.
- Other info: This is a permanent role offering high visibility and leadership opportunities.
The predicted salary is between 48000 - 72000 £ per year.
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 webinars to connect with potential colleagues and learn about the latest trends and requirements in GMP compliance.
✨Tip Number 2
Familiarise yourself with the specific regulatory frameworks and quality systems relevant to the role. This could involve reviewing recent guidelines from the MHRA or EMA, as well as understanding the nuances of both clinical and commercial environments.
✨Tip Number 3
Prepare for interviews by practising responses to questions about your experience with audits and quality assurance processes. Be ready to discuss specific examples where you contributed to continuous improvement in quality systems.
✨Tip Number 4
Showcase your collaborative working style by highlighting past experiences where you successfully worked with cross-functional teams. Emphasise your communication skills and how they helped in achieving compliance and quality objectives.
We think you need these skills to ace Qualified Person
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly understand the responsibilities of a Qualified Person. Familiarise yourself with the key tasks mentioned in the job description, such as certification and release of medicinal products, and ensure you can demonstrate relevant experience.
Tailor Your CV: Customise your CV to highlight your significant GMP experience and knowledge of quality systems. Emphasise any previous roles where you acted as a QP or were involved in regulatory compliance, as this will make your application stand out.
Craft a Compelling Cover Letter: Write a cover letter that showcases your strong communication skills and collaborative working style. Mention specific examples of how you've contributed to quality improvement and compliance in past roles, aligning your experiences with the company's needs.
Proofread Your Application: Before submitting, carefully proofread your application materials for any errors or inconsistencies. A polished application reflects your attention to detail, which is crucial in the pharmaceutical industry.
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 both clinical and commercial environments, as this will demonstrate your suitability for the role.
✨Understand Regulatory Frameworks
Familiarise yourself with the relevant regulatory frameworks and quality systems that govern pharmaceutical manufacturing. Being able to discuss these in detail will show your depth of knowledge and commitment to compliance.
✨Emphasise Collaboration Skills
Since the role requires working closely with various functions like Quality Assurance and Regulatory Affairs, emphasise your strong communication skills and collaborative working style. Share examples of successful teamwork in past roles.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions related to quality assurance and compliance. Prepare to discuss how you would handle specific situations, such as a batch that does not meet quality standards, to showcase your problem-solving abilities.
