At a Glance
- Tasks: Lead the Quality Assurance team and oversee quality operations in biotech.
- Company: Dynamic UK-based biotechnology company focused on innovation.
- Benefits: Competitive salary, comprehensive benefits package, and career advancement opportunities.
- Why this job: Make a significant impact in the biotech field and ensure high-quality standards.
- Qualifications: Over 5 years of GMP experience in biotech or gene therapy required.
- Other info: Ideal for candidates with a strong background in CMC and MSAT.
The predicted salary is between 70000 - 90000 £ per year.
A biotechnology company based in the UK is seeking a Head of Quality to lead their Quality Assurance team. This role demands over 5 years of experience in GMP settings, particularly in biotech or gene therapy. You will oversee quality operations, manage audits, and liaise with clients on regulatory matters.
The position offers a competitive salary of £70,000 - £90,000, along with a comprehensive benefits package. Suitable candidates must have the right to work in the UK and a strong background in CMC and MSAT.
Head of Quality Assurance — Biotech GMP & CMC Leader in London employer: taylorollinson Ltd
Contact Detail:
taylorollinson Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Head of Quality Assurance — Biotech GMP & CMC Leader in London
✨Tip Number 1
Network like a pro! Reach out to industry contacts on LinkedIn or attend biotech events. We all know that sometimes it’s not just what you know, but who you know that can help you land that Head of Quality Assurance role.
✨Tip Number 2
Prepare for interviews by brushing up on GMP regulations and quality assurance best practices. We recommend doing mock interviews with friends or mentors to get comfortable discussing your experience in CMC and MSAT.
✨Tip Number 3
Showcase your leadership skills! When you get the chance to speak about your past roles, highlight how you’ve successfully managed teams and improved quality operations. We want to see that you can lead the charge in a fast-paced biotech environment.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Head of Quality Assurance — Biotech GMP & CMC Leader in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in GMP settings and biotech. We want to see how your background aligns with the role, so don’t be shy about showcasing your relevant skills!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for the Head of Quality Assurance role. We love seeing passion and clarity in your writing, so let your personality come through.
Showcase Your Achievements: When detailing your experience, focus on specific achievements in quality operations and audits. We’re looking for results-driven candidates, so share metrics or outcomes that demonstrate your impact!
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 the role. Plus, it’s super easy!
How to prepare for a job interview at taylorollinson Ltd
✨Know Your GMP Inside Out
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Be ready to discuss specific examples from your past experience where you've implemented GMP standards, especially in biotech or gene therapy settings. This will show that you’re not just familiar with the regulations but can apply them effectively.
✨Showcase Your Leadership Skills
As a Head of Quality, you'll need to demonstrate strong leadership capabilities. Prepare to share instances where you've successfully led a team through audits or quality operations. Highlight how you managed challenges and motivated your team to achieve compliance and excellence.
✨Understand CMC and MSAT
Since the role requires a solid background in Chemistry, Manufacturing, and Controls (CMC) and Manufacturing Science and Technology (MSAT), be prepared to discuss your experience in these areas. Bring examples of how you've contributed to product development and regulatory submissions, as this will be crucial for the interview.
✨Prepare for Client Interactions
You'll be liaising with clients on regulatory matters, so practice articulating complex information clearly and confidently. Think about how you would handle difficult conversations or questions from clients, and be ready to demonstrate your communication skills during the interview.