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- Tasks: Make critical quality decisions and ensure regulatory compliance for imported pharmaceuticals.
- Company: Leading biopharma company in the UK with a focus on innovation.
- Benefits: Competitive salary, professional development, and opportunities for travel.
- Why this job: Join a dynamic team and make a real impact in the biopharma industry.
- Qualifications: Strong understanding of GMP guidelines and excellent stakeholder management skills.
- Other info: Opportunity to work autonomously and drive continuous improvement.
The predicted salary is between 43200 - 72000 £ per year.
A leading biopharma company in the UK is searching for a Qualified Person to join their QP Importation team. This role entails critical quality decision-making and regulatory compliance for imported pharmaceutical products.
The ideal candidate will have a strong grasp of GMP guidelines and regulator requirements. With a need for excellent stakeholder management skills, this position offers the opportunity to work autonomously with a focus on continuous improvement.
The role involves regular interactions across functional teams and periodic travel to various sites.
Lead Qualified Person, UK QP Importation & Release employer: Gsk
Contact Detail:
Gsk Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Lead Qualified Person, UK QP Importation & Release
✨Tip Number 1
Network like a pro! Reach out to professionals in the biopharma industry on LinkedIn or at events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on GMP guidelines and regulatory compliance. We recommend practising common interview questions related to quality decision-making, so you can showcase your expertise confidently.
✨Tip Number 3
Show off your stakeholder management skills! During interviews, share examples of how you've successfully collaborated with different teams. We want to see how you can bring people together for continuous improvement.
✨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 about their job search.
We think you need these skills to ace Lead Qualified Person, UK QP Importation & Release
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience with GMP guidelines and regulatory compliance. We want to see how your skills align with the role of a Qualified Person, so don’t hold back on showcasing your relevant achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for our QP Importation team. Share specific examples of your stakeholder management skills and how you've contributed to continuous improvement in previous roles.
Showcase Your Decision-Making Skills: In your application, highlight instances where you’ve made critical quality decisions. We’re looking for someone who can demonstrate their ability to navigate complex regulatory environments, so be sure to include relevant experiences.
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 this exciting opportunity. Plus, it’s super easy to do!
How to prepare for a job interview at Gsk
✨Know Your GMP Guidelines
Make sure you brush up on Good Manufacturing Practice (GMP) guidelines before the interview. Being able to discuss these in detail will show that you have the necessary knowledge for the role and can make informed quality decisions.
✨Showcase Stakeholder Management Skills
Prepare examples of how you've successfully managed stakeholders in previous roles. This could include resolving conflicts or ensuring compliance with regulatory requirements. Highlighting these experiences will demonstrate your ability to work effectively across functional teams.
✨Understand Regulatory Compliance
Familiarise yourself with the specific regulatory requirements relevant to imported pharmaceutical products. Being able to articulate how you ensure compliance will set you apart as a candidate who is proactive and knowledgeable.
✨Emphasise Continuous Improvement
Think of instances where you've contributed to process improvements in your past roles. Discussing your commitment to continuous improvement will resonate well, especially since the role focuses on enhancing quality and efficiency.
