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- Tasks: Ensure quality and compliance in the production of Sterile Pharmaceuticals.
- Company: Join a leading pharmaceutical company in the UK focused on quality assurance.
- Benefits: Be part of a dynamic team with opportunities for growth in the STEM sector.
- Why this job: Make a real impact in healthcare by ensuring the safety of medicinal products.
- Qualifications: Relevant degree in science 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 (QP) to join a leading pharmaceutical company based in the UK. As the Qualified Person (QP) you will be responsible for:
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person (QP) will be varied however the key duties and responsibilities are as follows:
1. Perform QP batch release and support the day-to-day operation of the Quality Management System.
2. Carry out the duties as described in the QP Code of Practice and Eudralex Volume 4 GMP guideline for QPs (Annex 16).
3. Undertake routine product certification as a Qualified Person in accordance with article 51 of 2001/83/EC and Annex 16 of Good Manufacturing Practice Part I (EudraLex volume 4).
4. Assist and lead in maintaining GMP & GDP standards across all site operations.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Qualified Person (QP) we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific discipline.
2. Proven industry experience in pharmaceutical quality assurance.
3. An Eligible Qualified Person (QP) within the UK.
Key Words:
Qualified Person / QP / Pharmaceutical Quality Assurance / GMP / GDP / Batch Release / Quality Management System / Eudralex / Regulatory Compliance / Hybrid
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 highlight your relevant experience in pharmaceutical manufacturing and quality assurance during networking events. Connect with professionals in the industry who can provide insights and potentially refer you to opportunities.
✨Tip Number 2
Stay updated on the latest regulations and guidelines related to pharmaceutical quality and compliance. This knowledge will not only help you in interviews but also demonstrate your commitment to the field.
✨Tip Number 3
Consider joining professional organizations or forums related to pharmaceutical quality management. Engaging in discussions and sharing your expertise can help you build a network that may lead to job opportunities.
✨Tip Number 4
Prepare for potential interviews by practicing answers to common questions about quality assurance processes and regulatory compliance. Being well-prepared will boost your confidence and help you stand out as a candidate.
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 Skills: List your skills related to quantitative and qualitative analyses of active substances. Mention any specific methodologies or technologies you are familiar with that are relevant to the role of a Qualified Person.
Tailor Your Application: Customize your CV and cover letter to align with the job description. Use keywords from the job listing, such as 'Quality Assurance', 'Regulatory Compliance', and 'Pharmaceutical Manufacturing', to ensure your application stands out.
How to prepare for a job interview at Hyper Recruitment Solutions
✨Know Your Regulations
Familiarize yourself with the relevant regulations and guidelines that govern pharmaceutical manufacturing and quality assurance. Being able to discuss these confidently will demonstrate your expertise and commitment to compliance.
✨Prepare for Technical Questions
Expect technical questions related to batch release processes, quality management systems, and analytical methods. Brush up on your knowledge of quantitative and qualitative analyses to showcase your practical experience.
✨Showcase Problem-Solving Skills
Be ready to discuss past experiences where you investigated and resolved quality issues. Highlight your analytical thinking and how you approached deviations in manufacturing processes.
✨Engage in Audit Discussions
Since participating in audits is a key responsibility, prepare to talk about your experiences with internal and external audits. Discuss how you contributed to improving quality systems and compliance during these processes.
