Quality Lead for Regenerative Medicine CDMO (MHRA-ready) in Stevenage
Quality Lead for Regenerative Medicine CDMO (MHRA-ready)

Quality Lead for Regenerative Medicine CDMO (MHRA-ready) in Stevenage

Stevenage Full-Time 42000 - 84000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead quality assurance efforts and ensure compliance with MHRA regulations.
  • Company: Pioneering regenerative medicine company in Stevenage with a focus on innovation.
  • Benefits: Competitive salary, stock options, and a collaborative work environment.
  • Why this job: Join a cutting-edge field and make a real difference in regenerative medicine.
  • Qualifications: Significant QA experience and strong understanding of MHRA regulations.
  • Other info: Dynamic team focused on continuous improvement and career growth.

The predicted salary is between 42000 - 84000 £ per year.

A pioneering regenerative medicine company in Stevenage is looking for a Quality Assurance Lead to drive regulatory compliance and quality strategy. You will oversee the establishment of quality systems necessary for obtaining the MHRA Manufacturing and Import Authorisation license.

The ideal candidate has significant QA experience and a strong understanding of MHRA regulations. This role offers a competitive salary with stock options and a collaborative environment focused on continuous improvement.

Quality Lead for Regenerative Medicine CDMO (MHRA-ready) in Stevenage employer: Cytera CellWorks

Join a pioneering regenerative medicine company in Stevenage, where you will be part of a collaborative environment dedicated to continuous improvement and innovation. We offer competitive salaries, stock options, and ample opportunities for professional growth, making us an excellent employer for those looking to make a meaningful impact in the field of quality assurance and regulatory compliance.
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Contact Detail:

Cytera CellWorks Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Quality Lead for Regenerative Medicine CDMO (MHRA-ready) in Stevenage

✨Tip Number 1

Network like a pro! Reach out to professionals in the regenerative medicine field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that Quality Lead role.

✨Tip Number 2

Prepare for interviews by brushing up on MHRA regulations and quality assurance best practices. We recommend creating a cheat sheet of key points to discuss, so you can showcase your expertise confidently.

✨Tip Number 3

Don’t just apply anywhere; focus on companies that align with your values and career goals. We suggest checking out our website for tailored job listings that fit your skills in quality assurance and regulatory compliance.

✨Tip Number 4

Follow up after interviews! A quick thank-you email can set you apart from other candidates. We believe it shows your enthusiasm for the role and keeps you fresh in their minds.

We think you need these skills to ace Quality Lead for Regenerative Medicine CDMO (MHRA-ready) in Stevenage

Quality Assurance
Regulatory Compliance
MHRA Regulations
Quality Systems Development
Continuous Improvement
Collaboration Skills
Analytical Skills
Problem-Solving Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your QA experience and understanding of MHRA regulations. We want to see how your background aligns with the role, so don’t be shy about 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 regenerative medicine and how you can contribute to our quality strategy. Keep it engaging and personal – we love to see your personality!

Showcase Continuous Improvement Mindset: In your application, mention any initiatives or projects where you’ve driven continuous improvement in quality systems. We’re all about innovation, so let us know how you’ve made a difference in your previous roles!

Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!

How to prepare for a job interview at Cytera CellWorks

✨Know Your MHRA Regulations

Make sure you brush up on the latest MHRA regulations before your interview. Being able to discuss specific compliance requirements and how they relate to quality assurance will show that you’re not just familiar with the standards, but that you can actively contribute to the company’s regulatory strategy.

✨Showcase Your QA Experience

Prepare to share detailed examples of your previous QA experience, especially in a CDMO setting. Highlight any successful projects where you implemented quality systems or improved compliance processes. This will demonstrate your hands-on expertise and how it aligns with the role.

✨Emphasise Continuous Improvement

Since the company values continuous improvement, come ready with ideas or examples of how you've driven quality enhancements in past roles. Discussing specific methodologies or tools you've used will illustrate your proactive approach and fit within their collaborative environment.

✨Ask Insightful Questions

Prepare thoughtful questions about the company's quality strategy and future goals. This not only shows your genuine interest in the role but also gives you a chance to assess if the company culture aligns with your values, particularly around quality assurance and regulatory compliance.

Quality Lead for Regenerative Medicine CDMO (MHRA-ready) in Stevenage
Cytera CellWorks
Location: Stevenage
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  • Quality Lead for Regenerative Medicine CDMO (MHRA-ready) in Stevenage

    Stevenage
    Full-Time
    42000 - 84000 £ / year (est.)
  • C

    Cytera CellWorks

    50-100
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