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- Tasks: Certify drug products and lead quality assurance initiatives in a dynamic environment.
- Company: Leading pharmaceutical CDMO in the UK with a focus on innovation.
- Benefits: Competitive salary, generous pension scheme, and exceptional career growth opportunities.
- Why this job: Make a real impact in the pharmaceutical industry while ensuring regulatory compliance.
- Qualifications: Strong background in pharmaceutical manufacturing and knowledge of cGMP.
- Other info: Join a team dedicated to quality and compliance at a pivotal site.
The predicted salary is between 80000 - 90000 £ per year.
A leading pharmaceutical CDMO in the UK is seeking a Qualified Person for its Holmes Chapel site. This pivotal role involves certifying drug products, ensuring regulatory compliance, and leading quality assurance initiatives.
Ideal candidates will have a strong background in pharmaceutical manufacturing, knowledge of cGMP, and regulatory experience.
The position offers a competitive salary between £80k to £90k along with additional benefits including a generous pension scheme and the opportunity for exceptional career growth.
Qualified Person – Lead Quality & Compliance, pMDI Innovation in London employer: Bespak
Contact Detail:
Bespak Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person – Lead Quality & Compliance, pMDI Innovation in London
✨Tip Number 1
Network like a pro! Reach out to industry contacts on LinkedIn or attend local pharmaceutical events. We all know that sometimes it’s not just what you know, but who you know that can help you land that Qualified Person role.
✨Tip Number 2
Prepare for the interview by brushing up on your cGMP knowledge and regulatory compliance. We recommend practising common interview questions related to quality assurance initiatives so you can showcase your expertise confidently.
✨Tip Number 3
Don’t forget to follow up after your interviews! A quick thank-you email can go a long way in keeping you top of mind. We suggest mentioning something specific from your conversation to make it personal.
✨Tip Number 4
Apply through our website for the best chance at landing that job! We’ve got all the latest openings, and applying directly shows your enthusiasm for the role. Plus, it’s super easy to navigate!
We think you need these skills to ace Qualified Person – Lead Quality & Compliance, pMDI Innovation in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in pharmaceutical manufacturing and regulatory compliance. We want to see how your background aligns with the role of Qualified Person, so don’t hold back on showcasing relevant achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about quality assurance and how your skills can contribute to our team. We love hearing personal stories that connect you to the role.
Showcase Your cGMP Knowledge: Since this role involves ensuring compliance with cGMP, make sure to mention any specific experiences or training you have in this area. We’re looking for candidates who can hit the ground running!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just a few clicks and you’re done!
How to prepare for a job interview at Bespak
✨Know Your cGMP Inside Out
Make sure you brush up on your knowledge of current Good Manufacturing Practices (cGMP). Be prepared to discuss how you've applied these principles in your previous roles, as this will show your understanding of regulatory compliance and quality assurance.
✨Showcase Your Leadership Skills
As a Qualified Person, you'll be leading quality assurance initiatives. Think of examples from your past experiences where you've successfully led a team or project. Highlight your ability to motivate others and drive compliance within a team setting.
✨Prepare for Regulatory Questions
Expect questions about regulatory frameworks and how they impact pharmaceutical manufacturing. Familiarise yourself with the latest regulations and be ready to discuss how you've navigated compliance challenges in the past.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions that demonstrate your interest in the role and the company. Inquire about their quality assurance processes or future projects in pMDI innovation. This shows you're not just interested in the job, but also in contributing to their success.
