At a Glance
- Tasks: Lead quality engineering efforts and ensure compliance in the medical device industry.
- Company: Kinetica, a leader in medical device innovation.
- Benefits: Gain valuable experience in a dynamic field with potential for future opportunities.
- Other info: Onsite role in York with a contract duration of 6-9 months.
- Why this job: Make a real difference in healthcare by ensuring product quality and safety.
- Qualifications: Experience in quality engineering and knowledge of ISO 13485 required.
The predicted salary is between 40000 - 50000 £ per year.
Kinetica is looking for an experienced Quality Engineer to join their team in York and North Yorkshire for a 6-9 month contract in the medical device industry. The ideal candidate will have extensive knowledge in quality engineering, including validation programmes and compliance with ISO 13485.
This role requires working onsite 5 days a week. You will lead risk management activities, drive continuous improvements, and ensure compliance during audits, all while supporting projects to ensure timely delivery.
Medical Device Quality Engineer – Validation Lead (Contract) employer: Kinetica
Kinetica is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals in the medical device industry. With a strong focus on employee growth and development, Kinetica offers opportunities to lead impactful projects while ensuring compliance with industry standards. Located in the vibrant region of York and North Yorkshire, employees benefit from a supportive environment that values quality and continuous improvement.
StudySmarter Expert Advice🤫
We think this is how you could land Medical Device Quality Engineer – Validation Lead (Contract)
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical device industry on LinkedIn or at local meetups. We can’t stress enough how valuable personal connections can be in landing that Quality Engineer role.
✨Tip Number 2
Prepare for interviews by brushing up on ISO 13485 and validation programmes. We recommend creating a cheat sheet of key points and examples from your experience to showcase your expertise during the interview.
✨Tip Number 3
Don’t just apply; follow up! After submitting your application through our website, drop a quick email to express your enthusiasm. It shows initiative and keeps you on their radar.
✨Tip Number 4
Showcase your problem-solving skills! Be ready to discuss specific challenges you've faced in quality engineering and how you overcame them. We want to see your ability to drive continuous improvements in action!
We think you need these skills to ace Medical Device Quality Engineer – Validation Lead (Contract)
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your experience in quality engineering and validation programmes. We want to see how your skills align with the requirements of the Medical Device Quality Engineer role, so don’t hold back on showcasing your knowledge of ISO 13485!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for Kinetica. Share specific examples of how you've led risk management activities or driven continuous improvements in past roles. We love a good story!
Showcase Your Compliance Knowledge:Since compliance is key in this role, make sure to mention any relevant experiences you have with audits and regulatory standards. We’re looking for someone who can ensure compliance effortlessly, so let us know how you’ve done this before!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you don’t miss out on any important updates. Plus, we love seeing applications come through our platform!
How to prepare for a job interview at Kinetica
✨Know Your Standards
Familiarise yourself with ISO 13485 and other relevant regulations. Be ready to discuss how you've applied these standards in your previous roles, especially in validation programmes.
✨Showcase Your Experience
Prepare specific examples from your past work that highlight your experience in quality engineering and risk management. Use the STAR method (Situation, Task, Action, Result) to structure your responses.
✨Continuous Improvement Mindset
Be prepared to talk about how you've driven continuous improvements in your previous positions. Think of concrete examples where your initiatives led to better compliance or efficiency.
✨Engage with the Team
Since this role requires onsite collaboration, demonstrate your ability to work well in a team. Ask questions about the team dynamics and how you can contribute to a positive working environment.
