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- Tasks: Ensure quality and compliance in sterile pharmaceutical production.
- Company: Join a leading UK pharmaceutical company focused on quality and innovation.
- Benefits: Gain experience in a dynamic environment with opportunities for growth.
- Why this job: Make a real impact in healthcare while working with cutting-edge products.
- Qualifications: Relevant scientific degree and experience in pharmaceutical manufacturing required.
- Other info: We value diversity and encourage all qualified candidates to apply.
The predicted salary is between 36000 - 60000 £ per year.
We are currently looking for a Qualified Person to join a leading pharmaceutical company based in the UK. As the Qualified Person, you will be responsible for ensuring the highest standards of quality and compliance in the production of Sterile Pharmaceuticals. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Qualified Person will be varied however the key duties and responsibilities are as follows: 1. Overseeing the release of medicinal products for distribution, ensuring compliance with all relevant regulations and guidelines. 2. Reviewing and approving batch records, analytical data, and other documentation related to the manufacturing and testing of medicinal products. 3. Investigating and resolving quality issues and deviations related to manufacturing processes and materials. 4. Participating in internal and external audits of the manufacturing facilities and quality systems. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Qualified Person we are looking to identify the following on your profile and past history: 1. Relevant degree in a scientific discipline such as pharmacy, medicine, chemistry, pharmaceutical chemistry, or biology. 2. Proven industry experience in pharmaceutical manufacturing, quality assurance, and regulatory compliance. 3. A working knowledge and practical experience with quantitative and qualitative analyses of active substances and the necessary testing and checking to ensure the quality of medicinal products. Key Words: Qualified Person / QP / Pharmaceuticals / Quality Management System / Batch Release / Pharmaceutical Manufacturing / Quality Assurance / Regulatory Compliance / MHRA Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Qualified Person/QP employer: Hyper Recruitment Solutions
Contact Detail:
Hyper Recruitment Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person/QP
✨Tip Number 1
Make sure to familiarize yourself with the latest regulations and guidelines related to pharmaceutical manufacturing and quality assurance. This knowledge will not only help you in interviews but also demonstrate your commitment to compliance.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who are already working as Qualified Persons. They can provide valuable insights into the role and may even refer you to job openings.
✨Tip Number 3
Prepare for potential technical questions during the interview by reviewing common quality assurance practices and case studies related to batch release and quality management systems.
✨Tip Number 4
Showcase any relevant certifications or training you have completed in quality assurance or regulatory compliance. This can set you apart from other candidates and highlight your dedication to the field.
We think you need these skills to ace Qualified Person/QP
Some tips for your application 🫡
Highlight Relevant Experience: Make sure to emphasize your experience in pharmaceutical manufacturing and quality assurance. Use specific examples that demonstrate your knowledge of regulatory compliance and your role in batch release processes.
Showcase Your Education: Clearly state your relevant degree in a scientific discipline. If you have additional certifications or training related to quality management systems or regulatory compliance, include those as well.
Detail Your Analytical Skills: Discuss your practical experience with quantitative and qualitative analyses of active substances. Provide examples of how you've ensured the quality of medicinal products through testing and documentation.
Tailor Your Application: Customize your CV and cover letter to reflect the key duties and responsibilities mentioned in the job description. Use keywords from the listing, such as 'Quality Assurance' and 'Regulatory Compliance', to align your application with what the company is looking for.
How to prepare for a job interview at Hyper Recruitment Solutions
✨Showcase Your Relevant Experience
Make sure to highlight your previous experience in pharmaceutical manufacturing and quality assurance. Be prepared to discuss specific examples of how you've ensured compliance with regulations and resolved quality issues.
✨Demonstrate Your Knowledge of Regulations
Familiarize yourself with the relevant regulations and guidelines that govern the release of medicinal products. During the interview, confidently discuss how you have applied these regulations in your past roles.
✨Prepare for Technical Questions
Expect technical questions related to batch records, analytical data, and quality management systems. Brush up on your knowledge of quantitative and qualitative analyses to effectively answer these questions.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's quality systems and audit processes. This shows your genuine interest in the role and helps you assess if the company aligns with your career goals.
