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- Tasks: Join a dynamic 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 the pharmaceutical industry while collaborating with diverse teams.
- Qualifications: Must be eligible to act as a QP in the UK with significant GMP experience.
- Other info: This is a permanent role offering high visibility and leadership opportunities.
The predicted salary is between 43200 - 72000 £ per year.
1 day ago Be among the first 25 applicants
Direct message the job poster from Nexia
Removing Recruitment Stress in Life Sciences – Director at Nexia
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
Seniority level
-
Seniority level
Mid-Senior level
Employment type
-
Employment type
Full-time
Job function
-
Job function
Science, Quality Assurance, and Supply Chain
-
Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Research Services
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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 will not only help you in interviews but also demonstrate your commitment to understanding the complexities of the pharmaceutical landscape.
✨Tip Number 3
Prepare for potential interview scenarios by reviewing common questions related to GMP compliance and quality assurance. Practising your responses can help you articulate your experience and knowledge effectively during the interview process.
✨Tip Number 4
Showcase your collaborative skills by discussing past experiences where you worked closely with cross-functional teams. Highlighting your ability to communicate and work effectively with Quality Assurance, Manufacturing, and Regulatory Affairs will set you apart from other candidates.
We think you need these skills to ace Qualified Person
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in GMP and pharmaceutical manufacturing. Emphasise your role in quality assurance and any specific achievements that demonstrate your ability to meet regulatory and internal quality requirements.
Craft a Compelling Cover Letter: In your cover letter, express your enthusiasm for the Qualified Person role and how your background aligns with the company's needs. Mention your experience with both clinical and commercial environments, and your understanding of quality systems and regulatory frameworks.
Highlight Key Skills: Clearly outline your strong communication skills and collaborative working style in your application. Provide examples of how you've successfully worked with cross-functional teams, particularly in high-pressure environments.
Showcase Continuous Improvement Initiatives: If you have experience in supporting continuous improvement of quality systems or manufacturing processes, make sure to include this in your application. Highlight specific initiatives you’ve led or contributed to that resulted in enhanced compliance or efficiency.
How to prepare for a job interview at Nexia
✨Showcase Your GMP Expertise
Make sure to highlight your significant GMP experience during the interview. Be prepared to discuss specific examples from your past roles where you ensured compliance with regulatory and internal quality requirements.
✨Demonstrate Collaborative Skills
Since the role requires working closely with various departments, emphasise your strong communication skills and collaborative working style. Share instances where you successfully collaborated with Quality Assurance, Manufacturing, or Regulatory Affairs teams.
✨Prepare for Regulatory Questions
Expect questions related to regulatory frameworks and quality systems. Brush up on current regulations and be ready to explain how you have navigated these in previous positions, particularly in relation to product release.
✨Emphasise Continuous Improvement
Discuss your commitment to continuous improvement in quality systems and manufacturing processes. Provide examples of initiatives you've led or contributed to that enhanced compliance or efficiency in your previous roles.
