At a Glance
- Tasks: Ensure compliance with quality systems and support R&D teams in device development.
- Company: Teva Pharmaceuticals, a leader in the healthcare industry.
- Benefits: Generous leave, flexible working hours, and a supportive work environment.
- Other info: Great opportunity for career growth in a leading pharmaceutical company.
- Why this job: Join a dynamic team and make a difference in medical device innovation.
- Qualifications: Relevant degree and experience in medical device GMP required.
The predicted salary is between 50000 - 65000 € per year.
Teva Pharmaceuticals in Preston Brook is looking for a Quality Manager in Device R&D. The role involves ensuring compliance with the Quality Management System for combination products, offering guidance and support to R&D teams.
Applicants should have a relevant degree, significant experience in medical device GMP, and strong knowledge of regulatory requirements.
Benefits include generous leave and flexible working arrangements.
Quality Manager, Device R&D — GMP Leader, Flexible Hours employer: Teva Pharmaceuticals
Teva Pharmaceuticals is an exceptional employer, offering a dynamic work environment in Preston Brook where innovation meets compliance. With flexible working hours and generous leave policies, we prioritise employee well-being while fostering professional growth through continuous learning opportunities in the medical device sector. Join us to be part of a collaborative culture that values your expertise and contributions in ensuring the highest quality standards for our products.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Manager, Device R&D — GMP Leader, Flexible Hours
✨Tip Number 1
Network like a pro! Reach out to folks in the industry, especially those at Teva Pharmaceuticals. A friendly chat can sometimes open doors that a CV can't.
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of GMP and regulatory requirements. We want you to shine when discussing how your experience aligns with the role!
✨Tip Number 3
Showcase your leadership skills! Think of examples where you've guided teams or improved processes. This is key for a Quality Manager role, and we want to hear your stories.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you're serious about joining the team at Teva.
We think you need these skills to ace Quality Manager, Device R&D — GMP Leader, Flexible Hours
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your relevant experience in medical device GMP and regulatory requirements. We want to see how your background aligns with the Quality Manager role, so don’t be shy about showcasing your achievements!
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 at Teva Pharmaceuticals. Keep it engaging and personal.
Showcase Your Soft Skills:While technical skills are crucial, we also value strong communication and leadership abilities. Make sure to include examples of how you've guided teams or improved processes in your previous roles.
Apply Through Our Website:We encourage you to apply directly through our website for a smoother application process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates!
How to prepare for a job interview at Teva Pharmaceuticals
✨Know Your GMP Inside Out
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Be ready to discuss how you've applied these principles in past roles, especially in relation to medical devices. This will show that you’re not just familiar with the regulations but can also implement them effectively.
✨Showcase Your R&D Experience
Prepare specific examples from your experience in Device R&D. Think about challenges you've faced and how you overcame them. This will demonstrate your problem-solving skills and your ability to guide teams through compliance issues.
✨Understand Regulatory Requirements
Familiarise yourself with the latest regulatory requirements relevant to combination products. Being able to discuss these in detail will highlight your expertise and commitment to quality management, which is crucial for the role.
✨Emphasise Flexibility and Team Support
Since the role offers flexible hours, be prepared to discuss how you manage your time effectively while supporting your team. Share examples of how you’ve fostered collaboration and maintained quality standards, even in a flexible working environment.
