Quality Lead, Regenerative Medicine CDMO — MHRA MIA Readiness in London
Quality Lead, Regenerative Medicine CDMO — MHRA MIA Readiness

Quality Lead, Regenerative Medicine CDMO — MHRA MIA Readiness in London

London Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead quality assurance efforts and ensure compliance with MHRA MIA licensing.
  • Company: Pioneering biotechnology firm in Greater London with a focus on innovation.
  • Benefits: Competitive salary, stock options, and opportunities for professional growth.
  • Why this job: Join a fast-paced environment and make a significant impact in regenerative medicine.
  • Qualifications: Significant QA experience and strong knowledge of MHRA and EU GMP.
  • Other info: Dynamic role with potential for career advancement in a cutting-edge industry.

The predicted salary is between 36000 - 60000 £ per year.

A pioneering biotechnology firm in Greater London seeks an experienced Quality Assurance Lead to oversee compliance and lead the path to MHRA MIA licensing. This role will involve establishing quality protocols and ensuring production aligns with stringent regulations.

Ideal candidates have significant QA experience, strong knowledge of MHRA and EU GMP, and thrive in fast-paced environments.

Competitive salary with benefits including stock options and professional growth potential.

Quality Lead, Regenerative Medicine CDMO — MHRA MIA Readiness in London employer: Mytos & Aspen

Join a pioneering biotechnology firm in Greater London that values innovation and compliance, offering a dynamic work culture where your expertise in Quality Assurance will directly impact the future of regenerative medicine. With competitive salaries, stock options, and ample opportunities for professional growth, this company is dedicated to fostering an environment where employees can thrive and contribute to meaningful advancements in healthcare.
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Contact Detail:

Mytos & Aspen Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Quality Lead, Regenerative Medicine CDMO — MHRA MIA Readiness in London

Tip Number 1

Network like a pro! Reach out to industry professionals on LinkedIn or attend local biotech events. We can’t stress enough how personal connections can open doors to opportunities that aren’t even advertised.

Tip Number 2

Prepare for interviews by researching the company and its products. We recommend practising common interview questions related to quality assurance and MHRA regulations. The more you know, the more confident you'll feel!

Tip Number 3

Showcase your expertise! Bring examples of how you've established quality protocols in previous roles. We love seeing candidates who can demonstrate their impact on compliance and production standards.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate individuals ready to make a difference in the biotech field.

We think you need these skills to ace Quality Lead, Regenerative Medicine CDMO — MHRA MIA Readiness in London

Quality Assurance
MHRA Knowledge
EU GMP Knowledge
Regulatory Compliance
Quality Protocols Establishment
Production Alignment
Fast-Paced Environment Adaptability
Leadership Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your relevant QA experience and knowledge of MHRA and EU GMP. We want to see how your background aligns 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 assurance in regenerative medicine and how you can contribute to our mission. Keep it engaging and personal.

Showcase Your Fast-Paced Experience: Since we thrive in fast-paced environments, make sure to include examples of how you've successfully managed challenges in similar settings. We love to see candidates who can adapt and excel under pressure!

Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of applications and ensures you get the attention you deserve. Plus, it’s super easy!

How to prepare for a job interview at Mytos & Aspen

Know Your Regulations

Make sure you brush up on your knowledge of MHRA and EU GMP regulations. Being able to discuss these in detail will show that you’re not just familiar with the standards but can also apply them effectively in a fast-paced environment.

Showcase Your QA Experience

Prepare specific examples from your past roles where you successfully established quality protocols or led compliance initiatives. This will help demonstrate your hands-on experience and how it aligns with the responsibilities of the Quality Lead position.

Emphasise Adaptability

Since this role is in a fast-paced setting, be ready to discuss how you've adapted to changes in previous jobs. Share stories that highlight your ability to thrive under pressure while maintaining high-quality standards.

Ask Insightful Questions

Prepare thoughtful questions about the company’s current quality processes and future goals regarding MHRA MIA licensing. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.

Quality Lead, Regenerative Medicine CDMO — MHRA MIA Readiness in London
Mytos & Aspen
Location: London

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