At a Glance
- Tasks: Ensure compliance with Quality Management System for innovative combination products.
- Company: Leading biopharmaceutical company committed to diversity and quality.
- Benefits: Generous benefits, leadership opportunities, and a focus on diversity.
- Other info: Support quality compliance across R&D teams for impactful projects.
- Why this job: Join a dynamic team and make a difference in medical device quality.
- 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 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 extensive 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
✨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 to discuss how your experience aligns with the role's requirements. Confidence is key!
✨Tip Number 3
Showcase your leadership skills! Think of examples from your past experiences where you led a team or project successfully. We want to see how you can support quality compliance across R&D teams, so be ready to share those stories.
✨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 take that extra step to engage with us directly.
We think you need these skills to ace Quality Manager, Device R&D - Lead Design Controls
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 hold back on 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. Keep it engaging and personal – we love to see your personality come through!
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’s super easy – just follow the prompts and submit your materials!
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 any other regulatory standards that might come up during the interview. Being able to discuss these confidently will show your expertise and commitment to quality.
✨Showcase Your Leadership Skills
Since this role involves leadership, prepare examples of how you've successfully led teams or projects in the past. Think about challenges you faced and how you overcame them. This will demonstrate your ability to support quality compliance across R&D teams.
✨Prepare for Scenario-Based Questions
Expect questions that ask how you would handle specific situations related to quality management and compliance. Practise articulating your thought process and decision-making skills in these scenarios. This will help you convey your problem-solving abilities effectively.
✨Emphasise Your Commitment to Diversity
The company values diversity, so be ready to discuss how you’ve contributed to diverse teams or initiatives in the past. Highlighting your understanding of the importance of diversity in the workplace can set you apart as a candidate who aligns with their values.
