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- Tasks: Ensure compliance and release of sterile pharmaceutical products in a modern GMP facility.
- Company: Join Smart4 Sciences, a forward-thinking pharmaceutical manufacturer in Essex.
- Benefits: Enjoy a dynamic work environment with opportunities for professional growth and development.
- Why this job: Make a real impact on patient safety and quality in a cutting-edge industry.
- Qualifications: Must be eligible as a Qualified Person with experience in sterile manufacturing.
- Other info: Contact Gareth Gooley for a confidential discussion about this exciting opportunity.
The predicted salary is between 36000 - 60000 £ per year.
Qualified Person (QP) – Sterile Manufacturing
Are you a Qualified Person with experience in sterile pharmaceutical manufacturing? Looking to make an impact in a forward-thinking company where quality and patient safety come first?
Smart4 Sciences are working with a pharmaceutical manufacturer in Essex specialising in the production of sterile and non-sterile products. As part of their continued expansion, they\’re seeking an experienced and proactive Qualified Person to join their quality team.
The Role:
As a QP, you\’ll be responsible for ensuring that products released to market meet the highest standards of GMP compliance and patient safety. Working in a modern GMP facility, you will:
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Act as a QP for the certification and release of sterile pharmaceutical products
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Ensure full compliance with MHRA and EU GMP guidelines
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Liaise closely with QA, Production, and Regulatory Affairs teams
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Contribute to audits, inspections, and continuous improvement projects
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Support the development of junior QA staff and provide QP oversight where needed
About You:
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Eligible to act as a Qualified Person under Directive 2001/83/EC
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Prior experience working with sterile manufacturing (aseptic/terminally sterilised products) is desirable
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Strong working knowledge of EU GMP and UK pharmaceutical regulations
If you\’re a QP ready for your next challenge in a state-of-the-art sterile manufacturing environment, we\’d love to hear from you!
Apply today or contact Gareth Gooley on for a confidential discussion.
Qualified Person - Pharmaceuticals employer: Smart4Sciences
Contact Detail:
Smart4Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person - Pharmaceuticals
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who work in sterile manufacturing. Attend relevant conferences or seminars where you can meet potential colleagues and learn more about the company culture.
✨Tip Number 2
Research the latest trends and regulations in GMP compliance and patient safety. Being knowledgeable about current practices will not only boost your confidence but also impress the hiring team during any discussions.
✨Tip Number 3
Prepare to discuss specific examples from your previous experience that demonstrate your ability to ensure compliance with MHRA and EU GMP guidelines. Real-life scenarios can showcase your problem-solving skills and proactive approach.
✨Tip Number 4
Consider reaching out to current or former employees of the company for insights into their experiences. This can provide you with valuable information about the role and help you tailor your approach when applying.
We think you need these skills to ace Qualified Person - Pharmaceuticals
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in sterile pharmaceutical manufacturing and your eligibility to act as a Qualified Person. Use specific examples that demonstrate your knowledge of EU GMP and UK pharmaceutical regulations.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality and patient safety. Mention your previous roles and how they align with the responsibilities of the QP position, particularly your experience with audits and inspections.
Highlight Relevant Qualifications: Clearly state your qualifications and any certifications that make you eligible to act as a Qualified Person under Directive 2001/83/EC. This will help the hiring team quickly see your suitability for the role.
Proofread Your Application: Before submitting, carefully proofread your application materials for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in the pharmaceutical industry.
How to prepare for a job interview at Smart4Sciences
✨Know Your GMP Regulations
Make sure you have a solid understanding of Good Manufacturing Practice (GMP) regulations, especially those relevant to sterile manufacturing. Be prepared to discuss how you've applied these standards in your previous roles.
✨Showcase Your Experience
Highlight your experience in sterile pharmaceutical manufacturing during the interview. Be ready to provide specific examples of how you've ensured compliance and patient safety in your past positions.
✨Prepare for Technical Questions
Expect technical questions related to the certification and release of sterile products. Brush up on your knowledge of MHRA and EU guidelines, as well as any recent changes in regulations that may impact the role.
✨Demonstrate Team Collaboration
Since the role involves liaising with various teams, be prepared to discuss your experience working collaboratively with QA, Production, and Regulatory Affairs. Share examples of how you've contributed to audits and continuous improvement projects.
