At a Glance
- Tasks: Lead quality assurance for medical devices and ensure compliance with regulatory standards.
- Company: Join a leading pharmaceutical R&D company in a dynamic environment.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: 12-month contract with a supportive team and excellent career development opportunities.
- Why this job: Make a real impact in healthcare by ensuring the safety and quality of innovative products.
- Qualifications: Degree in science or engineering; experience in medical devices or pharma is a plus.
The predicted salary is between 28000 - 38000 £ per year.
We are looking for a Quality Engineer – Compliance to support medical device and combination product development programmes within a leading pharmaceutical R&D environment.
- Lead and support design control and risk management activities across device and combination product programmes.
- Prepare and review Design History File (DHF) and risk management documentation.
- Ensure compliance with quality systems and regulatory standards.
- Support design validation activities, including human factors/usability engineering.
- Assist with regulatory submissions, supplier assessments, and quality audits.
- Support investigations related to clinical and commercial device manufacturing.
Degree in a relevant science or engineering discipline.
Experience in medical devices, combination products, pharma, or biotech.
Knowledge of design controls and risk management.
If you have experience working in regulated device or combination product environments and are interested in a hybrid contract role in the Cambridge area, please apply or get in touch.
Graduate Engineer / Quality Engineer employer: Cpl Life Sciences
Join a leading pharmaceutical R&D environment that prioritises innovation and compliance in the medical devices sector. With a hybrid working model, employees enjoy a balanced work-life dynamic while benefiting from a culture of collaboration and continuous learning. The company offers robust growth opportunities, ensuring that you can advance your career while contributing to meaningful projects that impact patient care.
StudySmarter Expert Advice🤫
We think this is how you could land Graduate Engineer / Quality Engineer
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical devices and pharma sectors on LinkedIn. Join relevant groups and engage in discussions to get your name out there.
✨Tip Number 2
Prepare for interviews by brushing up on design controls and risk management. We recommend practising common interview questions related to quality engineering to boost your confidence.
✨Tip Number 3
Showcase your experience with real-life examples. When discussing your background, highlight specific projects or challenges you've tackled in regulated environments to impress potential employers.
✨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.
We think you need these skills to ace Graduate Engineer / Quality Engineer
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Quality Engineer role. Highlight any relevant experience in medical devices or combination products, and don’t forget to mention your knowledge of design controls and risk management!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about quality engineering in the medical field and how your background makes you a perfect fit for this role.
Showcase Relevant Skills:When filling out your application, be sure to showcase skills that align with the job description, like compliance with quality systems and regulatory standards. We want to see how you can contribute to our team!
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. We can’t wait to hear from you!
How to prepare for a job interview at Cpl Life Sciences
✨Know Your Stuff
Make sure you brush up on your knowledge of medical devices and combination products. Familiarise yourself with design controls and risk management processes, as these are crucial for the role. Being able to discuss specific examples from your experience will show that you’re not just knowledgeable but also practical.
✨Prepare for Compliance Questions
Since this role involves ensuring compliance with quality systems and regulatory standards, be ready to answer questions about your understanding of these areas. Think about past experiences where you’ve had to navigate compliance issues and how you handled them. This will demonstrate your capability in a regulated environment.
✨Showcase Your Team Spirit
Collaboration is key in R&D environments. Be prepared to discuss how you’ve worked with cross-functional teams in the past. Highlight any experiences where you’ve led or supported design validation activities, as this will show your ability to work effectively with others in achieving common goals.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions! Inquire about the company’s approach to design validation or how they handle supplier assessments. This shows your genuine interest in the role and helps you gauge if the company aligns with your career aspirations.
