Senior Quality Director

Senior Quality Director

Full-Time 72000 - 108000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead global quality functions and ensure compliance with industry standards.
  • Company: Dynamic pharmaceutical and biotech company focused on innovation.
  • Benefits: Competitive salary, career development, and a chance to shape quality systems.
  • Why this job: Make a real impact on product integrity and operational excellence.
  • Qualifications: Proven experience in senior quality roles and deep knowledge of regulatory compliance.
  • Other info: Opportunity to mentor a high-performing team in a collaborative environment.

The predicted salary is between 72000 - 108000 £ per year.

We are seeking an experienced and strategic Director of quality to lead our global manufacturing quality function and ensure full compliance with GMP, ISO standards, and regulatory expectations. This role offers the opportunity to shape quality systems across multiple sites while supporting innovation in pharmaceutical, biotech, and medical device manufacturing.

The Director will oversee enterprise-wide quality programs, including CAPA management, deviations, audits, supplier qualification, and compliance training. They will partner closely with Manufacturing, Technical Operations, and Supply Chain to embed a culture of quality, drive continuous improvement, and maintain inspection readiness at all times.

This is a senior, hands-on role that requires strategic vision, operational excellence, and a commitment to product integrity and regulatory compliance.

  • Lead and manage the global quality function across multiple manufacturing sites.
  • Ensure compliance with GMP, ISO standards, and global regulatory requirements.
  • Drive inspection readiness for internal and external audits.
  • Collaborate with cross-functional teams to implement quality initiatives and continuous improvement.
  • Mentor, develop, and lead a high-performing quality team.

Proven experience in a senior quality role within pharmaceutical, biotech, or medical device manufacturing. Deep knowledge of GMP, ISO standards, and regulatory compliance (FDA, EMA, etc.). Excellent communication and stakeholder management abilities.

This is an outstanding opportunity to lead a global quality function and make a measurable impact on operational excellence and product integrity.

Senior Quality Director employer: Green Life Science

As a leading player in the pharmaceutical, biotech, and medical device sectors, our company is an exceptional employer that prioritises innovation and quality. We foster a collaborative work culture that encourages continuous improvement and professional growth, offering our employees the chance to lead impactful quality initiatives across multiple global sites. With a commitment to regulatory compliance and product integrity, we provide a dynamic environment where your expertise can truly make a difference.
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Contact Detail:

Green Life Science Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Quality Director

✨Tip Number 1

Network like a pro! Reach out to your connections in the pharmaceutical, biotech, or medical device sectors. We all know that sometimes it’s not just what you know, but who you know that can help you land that Senior Quality Director role.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of GMP and ISO standards. We recommend creating a cheat sheet of key points and examples from your past experiences that showcase your strategic vision and operational excellence.

✨Tip Number 3

Showcase your leadership skills! Be ready to discuss how you've mentored and developed high-performing teams in the past. We want to hear about your approach to fostering a culture of quality and continuous improvement.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive and engaged with our company.

We think you need these skills to ace Senior Quality Director

GMP Compliance
ISO Standards Knowledge
Regulatory Compliance (FDA, EMA)
CAPA Management
Audit Management
Supplier Qualification
Quality Systems Development
Continuous Improvement
Inspection Readiness
Cross-Functional Collaboration
Team Leadership
Stakeholder Management
Operational Excellence
Strategic Vision

Some tips for your application 🫡

Tailor Your CV: Make sure your CV reflects the specific skills and experiences that align with the Senior Quality Director role. Highlight your experience in GMP, ISO standards, and any relevant regulatory compliance to show us you’re the perfect fit.

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to tell us why you’re passionate about quality in manufacturing and how your strategic vision can drive continuous improvement. Be sure to mention any leadership experiences that showcase your ability to mentor and develop teams.

Showcase Your Achievements: When detailing your past roles, focus on quantifiable achievements. Did you lead a successful audit or implement a new quality initiative? Let us know! Numbers and specific examples help us see the impact you've made in previous positions.

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 during the process. Plus, we love seeing candidates who take that extra step!

How to prepare for a job interview at Green Life Science

✨Know Your Standards

Make sure you brush up on GMP and ISO standards before the interview. Being able to discuss these in detail will show that you’re not just familiar with them, but that you can apply them strategically in a global context.

✨Showcase Your Leadership Skills

Prepare examples of how you've led quality teams in the past. Highlight your experience in mentoring and developing high-performing teams, as this is crucial for the role. Use specific metrics or outcomes to demonstrate your impact.

✨Collaboration is Key

Be ready to discuss how you’ve worked with cross-functional teams in previous roles. Share specific instances where your collaboration led to successful quality initiatives or continuous improvement projects.

✨Stay Inspection Ready

Talk about your approach to maintaining inspection readiness. Discuss any systems or processes you’ve implemented to ensure compliance and readiness for audits, as this will resonate well with the expectations of the role.

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