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- Tasks: Ensure quality assurance and regulatory compliance in a senior role within the Medical Affairs team.
- Company: Established pharmaceutical company based in Maidenhead with a strong reputation.
- Benefits: Flexible work options, competitive salary, and opportunities for professional growth.
- Why this job: Join a vital role that impacts healthcare and regulatory standards in the UK and Ireland.
- Qualifications: Extensive experience in GMP/GDP and strong knowledge of regulatory affairs required.
- Other info: Enjoy a mix of on-site and remote work in a supportive environment.
The predicted salary is between 48000 - 72000 £ per year.
A well-established pharmaceutical company in Maidenhead is seeking a Quality and Regulatory professional to join its Medical Affairs team. This role is crucial with responsibilities including acting as Responsible Person and ensuring Quality Assurance and Regulatory compliance.
The ideal candidate will have extensive experience in GMP/GDP, strong knowledge of regulatory affairs, and the ability to operate independently in a senior capacity. This position offers a blend of on-site and remote work.
Senior QA & Regulatory Affairs Lead - RP/RPi, UK & Ireland in Maidenhead employer: Jobster
Contact Detail:
Jobster Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior QA & Regulatory Affairs Lead - RP/RPi, UK & Ireland in Maidenhead
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmaceutical industry on LinkedIn or at local events. We can’t stress enough how personal connections can open doors for you.
✨Tip Number 2
Prepare for interviews by brushing up on your GMP/GDP knowledge and regulatory affairs. We recommend practising common interview questions and scenarios related to Quality Assurance to show you’re the right fit.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. We suggest using our website to find roles that excite you and match your expertise.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can leave a lasting impression. We believe it shows your enthusiasm and professionalism, which is key in the QA and Regulatory field.
We think you need these skills to ace Senior QA & Regulatory Affairs Lead - RP/RPi, UK & Ireland in Maidenhead
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in GMP/GDP and regulatory affairs. We want to see how your background aligns with the responsibilities of the Senior QA & Regulatory Affairs Lead role.
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 Medical Affairs team. Share specific examples of your past achievements that relate to the job description.
Showcase Your Independence: Since this role requires operating independently, make sure to mention instances where you've successfully managed projects or teams on your own. We love seeing candidates who can take initiative!
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 don’t miss out on any important updates from us!
How to prepare for a job interview at Jobster
✨Know Your GMP/GDP Inside Out
Make sure you brush up on your Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP). Be ready to discuss specific examples from your experience where you've ensured compliance, as this will show your depth of knowledge and practical application.
✨Understand Regulatory Affairs Like a Pro
Familiarise yourself with the latest regulations affecting the pharmaceutical industry in the UK and Ireland. Prepare to talk about how you've navigated regulatory challenges in the past, as this will demonstrate your expertise and ability to operate independently.
✨Showcase Your Leadership Skills
As a Senior QA & Regulatory Affairs Lead, you'll need to exhibit strong leadership qualities. Think of instances where you've led a team or project successfully, and be ready to share these stories. This will highlight your capability to take charge and guide others.
✨Prepare for Hybrid Work Discussions
Since this role offers a blend of on-site and remote work, be prepared to discuss how you manage your time and productivity in both settings. Share strategies that have worked for you in the past, as this will show you're adaptable and ready for the demands of the role.
