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- Tasks: Ensure quality and compliance in sterile pharmaceutical production.
- Company: Join a leading UK pharmaceutical company focused on quality assurance.
- Benefits: Gain experience in a dynamic industry with opportunities for growth.
- Why this job: Make a real impact on healthcare by ensuring product safety and quality.
- Qualifications: Relevant scientific degree and experience in pharmaceutical manufacturing required.
- Other info: We value diversity and welcome applications from all qualified candidates.
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 specific regulations and guidelines related to pharmaceutical manufacturing in the UK. Understanding the MHRA requirements will give you an edge during interviews.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who have experience as a Qualified Person. They can provide valuable insights and may even refer you to open positions.
✨Tip Number 3
Stay updated on the latest trends and technologies in quality assurance and regulatory compliance. This knowledge can help you stand out as a candidate who is proactive and informed.
✨Tip Number 4
Prepare for potential interview questions by reviewing common scenarios related to batch release and quality issues. Being able to discuss your problem-solving approach will demonstrate your expertise.
We think you need these skills to ace Qualified Person/QP
Some tips for your application 🫡
Understand the Role: Make sure you fully understand the responsibilities of a Qualified Person in the pharmaceutical industry. Familiarize yourself with key terms like batch release, quality assurance, and regulatory compliance to demonstrate your knowledge in your application.
Highlight Relevant Experience: In your CV and cover letter, emphasize your relevant degree and any industry experience you have in pharmaceutical manufacturing or quality assurance. Use specific examples to showcase your expertise in handling quality issues and compliance.
Tailor Your Application: Customize your application materials to reflect the key duties and requirements listed in the job description. Use keywords from the job posting, such as 'quality management system' and 'regulatory compliance', to ensure your application stands out.
Proofread Your Documents: Before submitting your application, carefully proofread your CV and cover letter for any errors or inconsistencies. A polished application reflects your attention to detail, which is crucial for a role focused on quality and compliance.
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.
