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- Tasks: Ensure quality management and compliance in a dynamic pharmaceutical environment.
- Company: Leading manufacturer in pharmaceuticals with a focus on sustainability.
- Benefits: Competitive salary, growth opportunities, and a chance to make a difference.
- Why this job: Join an innovative team and contribute to sustainable practices in the industry.
- Qualifications: Relevant scientific background and experience in GMP production.
- Other info: Exciting role with potential for career advancement in a thriving sector.
The predicted salary is between 36000 - 60000 £ per year.
A leading manufacturer in pharmaceuticals is looking for a QA Associate to ensure quality management and compliance in a dynamic and growth-oriented setting. You will oversee the GMP Quality Management System, manage quality events, and ensure compliance with regulatory requirements.
Ideal candidates will have a relevant scientific background and experience in a GMP production environment. This role offers the opportunity to work with an innovative company focused on sustainable practices.
GMP QA & Compliance Specialist in London employer: SRG
Contact Detail:
SRG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land GMP QA & Compliance Specialist in London
✨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 valuable personal connections can be in landing that QA & Compliance Specialist role.
✨Tip Number 2
Prepare for interviews by brushing up on GMP regulations and quality management systems. We recommend practising common interview questions related to compliance and quality assurance to show you’re the perfect fit for the dynamic environment.
✨Tip Number 3
Showcase your scientific background! When you get the chance, highlight your relevant experience in GMP production during conversations or interviews. We want to see how your skills align with the innovative practices of the company.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. We’re all about making the process smooth and straightforward for you.
We think you need these skills to ace GMP QA & Compliance Specialist in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant scientific background and any experience in GMP production. We want to see how your skills align with the role, so don’t be shy about showcasing your achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about quality management and compliance in pharmaceuticals. Let us know what excites you about working with an innovative company like ours.
Showcase Your Attention to Detail: In the world of GMP, attention to detail is key. When writing your application, make sure it’s free from typos and errors. This not only reflects your professionalism but also your commitment to quality.
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!
How to prepare for a job interview at SRG
✨Know Your GMP Basics
Make sure you brush up on Good Manufacturing Practices (GMP) before the interview. Understand the key principles and how they apply to quality management in pharmaceuticals. This will show your potential employer that you're not just familiar with the terms, but you can also apply them in a real-world setting.
✨Showcase Your Scientific Background
Be ready to discuss your relevant scientific experience in detail. Prepare examples of how your background has equipped you to handle quality events and compliance issues. This is your chance to demonstrate how your knowledge can contribute to their innovative practices.
✨Prepare for Compliance Questions
Expect questions about regulatory requirements and compliance challenges. Think of specific situations where you ensured compliance or improved processes. Use the STAR method (Situation, Task, Action, Result) to structure your answers clearly and effectively.
✨Emphasise Your Adaptability
In a dynamic and growth-oriented setting, adaptability is key. Be prepared to discuss how you've successfully navigated changes in previous roles. Highlight your ability to learn quickly and implement new practices, especially in a GMP production environment.
