At a Glance
- Tasks: Ensure compliance with Quality Management System for innovative medical devices.
- Company: Leading biopharmaceutical company committed to diversity and innovation.
- Benefits: Generous benefits package and opportunities for leadership development.
- Other info: Join a dynamic team focused on improving healthcare solutions.
- Why this job: Make a real impact on quality compliance in cutting-edge R&D projects.
- Qualifications: Experience in medical device GMP and knowledge of ISO13485 standards.
The predicted salary is between 60000 - 80000 € per year.
A leading biopharmaceutical company in the UK is seeking a Quality Manager for Device R&D. This role involves ensuring compliance with the Quality Management System (QMS) for combination products throughout their lifecycle.
Candidates should have significant experience in medical device GMP and thorough knowledge of regulatory standards such as ISO13485.
The position offers opportunities for leadership and supports quality compliance across R&D teams. Generous benefits and a commitment to diversity are included.
Quality Manager, Device R&D - Lead Design Controls in Runcorn employer: Teva Pharmaceuticals
As a leading biopharmaceutical company in the UK, we pride ourselves on fostering a dynamic work culture that prioritises innovation and quality. Our commitment to employee growth is evident through comprehensive training programmes and leadership opportunities, ensuring that our team members thrive in their careers. With generous benefits and a strong focus on diversity, we create an inclusive environment where every voice is valued, making us an exceptional employer for those seeking meaningful and rewarding work in the Device R&D sector.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Manager, Device R&D - Lead Design Controls in Runcorn
✨Tip Number 1
Network like a pro! Reach out to professionals in the biopharmaceutical field, especially those involved in Device R&D. Use platforms like LinkedIn to connect and engage with them; you never know who might have the inside scoop on job openings.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ISO13485 and other regulatory standards. We recommend creating a cheat sheet of key points and examples from your experience that demonstrate your expertise in quality management systems.
✨Tip Number 3
Showcase your leadership skills! During interviews, be ready to discuss how you've led teams or projects in the past. Highlight specific instances where you ensured compliance and improved quality processes in your previous roles.
✨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 about their job search and genuinely interested in joining our team.
We think you need these skills to ace Quality Manager, Device R&D - Lead Design Controls in Runcorn
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your experience in medical device GMP and knowledge of regulatory standards like ISO13485. We want to see how your background aligns with the Quality Manager role, so don’t be shy about showcasing relevant projects!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about quality management in Device R&D and how you can contribute to our team. We love hearing personal stories that connect your experience to our mission.
Showcase Leadership Skills:Since this role involves leadership, make sure to highlight any past experiences where you’ve led teams or projects. We’re looking for candidates who can inspire and support others in maintaining quality compliance across R&D teams.
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 gives you a chance to explore more about our company culture and values!
How to prepare for a job interview at Teva Pharmaceuticals
✨Know Your QMS Inside Out
Make sure you’re well-versed in the Quality Management System (QMS) relevant to combination products. Brush up on ISO13485 and be ready to discuss how your experience aligns with ensuring compliance throughout a product's lifecycle.
✨Showcase Your Leadership Skills
This role involves leading quality compliance across R&D teams, so prepare examples of how you've successfully led teams in the past. Think about specific challenges you faced and how you motivated your team to achieve quality goals.
✨Understand Regulatory Standards
Familiarise yourself with the regulatory standards that govern medical devices. Be prepared to discuss how you’ve navigated these regulations in previous roles and how you can apply that knowledge to ensure compliance in this position.
✨Emphasise Your Commitment to Diversity
The company values diversity, so think about how you can contribute to an inclusive workplace. Prepare to share your thoughts on fostering diversity within teams and how it can enhance quality management in R&D.
