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- Tasks: Ensure compliance and product quality as a Qualified Person in a leading pharmaceutical company.
- Company: Join a dynamic and growing pharmaceutical organisation in Greater London.
- Benefits: Competitive salary, flexible working, and comprehensive benefits package.
- Other info: Collaborate with cross-functional teams in a supportive work culture.
- Why this job: Play a key role in ensuring the highest standards of compliance and quality.
- Qualifications: QP status eligible and strong IMP experience in a GMP environment.
The predicted salary is between 60000 - 80000 £ per year.
We are seeking an experienced Qualified Person (QP) with IMP experience to join a leading pharmaceutical company in Greater London. This is a fantastic opportunity to play a key role in ensuring the highest standards of compliance and product quality within a dynamic and growing organisation.
Key Responsibilities:
- Act as a QP for the certification and release of IMPs in compliance with EU GMP regulations.
- Ensure adherence to quality standards, regulatory requirements, and clinical trial protocols.
- Work closely with cross-functional teams, including Regulatory Affairs, Manufacturing, and Quality Assurance.
Requirements:
- QP status eligible under Directive 2001/83/EC.
- Strong IMP experience within a GMP environment.
- Excellent knowledge of EU and UK pharmaceutical regulations.
Location: Greater London Area (4 days on-site, 1 day from home)
Competitive salary + benefits
Interested? Apply now...
QP employer: ARx Recruitment Services
Contact Detail:
ARx Recruitment Services Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QP
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work in QP roles or related fields. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of EU GMP regulations and IMP processes. We recommend practising common interview questions with a friend or in front of a mirror to boost your confidence.
✨Tip Number 3
Showcase your experience! When you get the chance to speak with potential employers, highlight your past achievements in ensuring compliance and product quality. Use specific examples to demonstrate your impact.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive and engaged in their job search.
We think you need these skills to ace QP
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your QP status and IMP experience. We want to see how your background aligns with the key responsibilities mentioned in the job description, so don’t hold back on showcasing your relevant skills!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for this role. Mention your experience with EU GMP regulations and how you’ve ensured compliance in previous positions. Let us know what excites you about joining our team!
Showcase Your Teamwork Skills: Since you'll be working closely with cross-functional teams, it’s important to highlight your collaboration skills. Share examples of how you've successfully worked with Regulatory Affairs, Manufacturing, or Quality Assurance in the past. We love a team player!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for this fantastic opportunity. Don’t miss out on the chance to join our dynamic organisation!
How to prepare for a job interview at ARx Recruitment Services
✨Know Your Regulations
Make sure you brush up on EU and UK pharmaceutical regulations, especially those related to IMPs. Being able to discuss these confidently will show that you’re not just familiar with the rules but can apply them in practice.
✨Showcase Your Experience
Prepare specific examples from your past roles where you ensured compliance and product quality. Highlighting your hands-on experience in a GMP environment will demonstrate your capability as a Qualified Person.
✨Cross-Functional Collaboration
Be ready to talk about how you've worked with teams like Regulatory Affairs, Manufacturing, and Quality Assurance. Sharing stories of successful collaborations will illustrate your ability to thrive in a dynamic environment.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s approach to compliance and quality assurance. This not only shows your interest but also gives you a chance to assess if the company aligns with your professional values.