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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 efficacy.
- Qualifications: Relevant scientific degree and experience in pharmaceutical manufacturing required.
- Other info: We are an Equal Opportunities employer, welcoming diverse applicants.
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 that a Qualified Person might face, such as handling quality deviations or participating in audits. Being ready with examples will showcase your expertise.
We think you need these skills to ace Qualified Person/QP
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant degree and industry experience in pharmaceutical manufacturing and quality assurance. Use keywords from the job description, such as 'Qualified Person', 'Quality Management System', and 'Regulatory Compliance' to catch the employer's attention.
Craft a Strong Cover Letter: In your cover letter, emphasize your experience with batch release and your ability to resolve quality issues. Mention specific examples of how you've ensured compliance with regulations in past roles to demonstrate your suitability for the position.
Highlight Relevant Skills: Clearly outline your skills related to quantitative and qualitative analyses of active substances. Discuss any practical experience you have with testing and checking processes that ensure the quality of medicinal products.
Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. 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
✨Know Your Regulations
Familiarize yourself with the relevant regulations and guidelines in pharmaceutical manufacturing. Be prepared to discuss how you ensure compliance in your previous roles, as this will demonstrate your understanding of the industry's standards.
✨Highlight Your Experience
Be ready to share specific examples from your past experience that showcase your expertise in quality assurance and regulatory compliance. Discuss any challenges you faced and how you resolved them, particularly in relation to batch release and quality issues.
✨Demonstrate Analytical Skills
Since the role requires a working knowledge of quantitative and qualitative analyses, be prepared to talk about your experience with these processes. Highlight any relevant tools or methodologies you have used to ensure the quality of medicinal products.
✨Prepare for Audit Questions
As the position involves participating in audits, think about your experiences with internal and external audits. Be ready to discuss how you contributed to these processes and any improvements you implemented based on audit findings.
