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- Tasks: Support validation activities for groundbreaking medical technology that changes lives.
- Company: Rapidly growing Medical Devices company in Oxford with a focus on innovation.
- Benefits: Comprehensive benefits package, including healthcare, life assurance, and generous annual leave.
- Why this job: Join a mission-driven team and make a real impact in the medical field.
- Qualifications: Hands-on experience in Process or Product Validation, ideally in regulated industries.
- Other info: On-site role with excellent career development opportunities and strong long-term stability.
The predicted salary is between 36000 - 60000 £ per year.
A rapidly growing Medical Devices company in Oxford is seeking a Validation Engineer to support validation activities on a cutting-edge medical technology set to transform the lives of hundreds of thousands of people in the UK and internationally.
We are particularly interested in speaking with candidates who have hands-on experience in Process Validation or Product Validation. Ideally, this experience will come from the Medical Devices or Biotech sectors, although we may also consider applicants from other highly regulated industries.
Experience in writing Master Validation Plans would be highly advantageous, but not essential. You will, however, be responsible for developing, executing, and maintaining validation plans, so prior experience in these areas is required.
Due to the hands-on nature of the role, this position is on-site five days per week. You will therefore need to live within a commutable distance of Oxford or be open to relocating.
You will work closely with another Validation Engineer and collaborate cross-functionally with Quality Assurance, R&D, and Supply Chain teams. Knowledge of ISO 13485 is highly desirable.
Holding a Six Sigma Green Belt or similar qualification that has supported your career in Validation Engineering would be beneficial.
This organisation is well-funded, scaling quickly, and offers strong long-term stability alongside excellent opportunities for career development. In addition, they provide a comprehensive benefits package including healthcare, life assurance, pension, and generous annual leave.
Given the level of interest expected for this role, we encourage early applications.
To discuss the position in more detail, contact Andrew Welsh, Director of Medical Devices, Biotech and DeepTech Recruitment at Newton Colmore.
Validation Engineer - Oxford - Medical Devices employer: Newton Colmore
Contact Detail:
Newton Colmore Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Validation Engineer - Oxford - Medical Devices
✨Tip Number 1
Network like a pro! Reach out to your connections in the medical devices or biotech sectors. We all know that sometimes it’s not just what you know, but who you know that can get you in the door.
✨Tip Number 2
Prepare for those interviews! Brush up on your knowledge of ISO 13485 and be ready to discuss your hands-on experience with process and product validation. We want you to shine when it comes to showcasing your skills!
✨Tip Number 3
Don’t forget to follow up! After an interview, shoot a quick thank-you email to express your appreciation. It shows you’re genuinely interested and keeps you fresh in their minds.
✨Tip Number 4
Apply through our website! We’ve got loads of opportunities waiting for you, and applying directly can sometimes give you an edge. Let’s get you that Validation Engineer role!
We think you need these skills to ace Validation Engineer - Oxford - Medical Devices
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Validation Engineer role. Highlight your hands-on experience in Process or Product Validation, especially if it’s from the Medical Devices or Biotech sectors. We want to see how your skills match what we’re looking for!
Showcase Relevant Experience: If you’ve got experience writing Master Validation Plans, don’t hold back! Even if it’s not essential, it’s a great way to stand out. Be sure to detail any relevant projects or roles that demonstrate your ability to develop and maintain validation plans.
Highlight Your Qualifications: If you hold a Six Sigma Green Belt or similar qualification, make it known! This can really boost your application. Also, mention any knowledge of ISO 13485 as it’s highly desirable for this position.
Apply Early!: Given the level of interest expected for this role, we encourage you to apply as soon as possible through our website. The sooner you get your application in, the better your chances of standing out!
How to prepare for a job interview at Newton Colmore
✨Know Your Validation Basics
Make sure you brush up on your knowledge of Process and Product Validation. Be ready to discuss specific examples from your past experience, especially if they relate to the Medical Devices or Biotech sectors. This will show that you understand the industry's standards and can hit the ground running.
✨Familiarise Yourself with ISO 13485
Since knowledge of ISO 13485 is highly desirable for this role, take some time to review its key principles and how they apply to validation processes. Being able to reference this during your interview will demonstrate your commitment to quality and compliance.
✨Prepare for Cross-Functional Collaboration
This role involves working closely with Quality Assurance, R&D, and Supply Chain teams. Think about how you've successfully collaborated in the past and be prepared to share those experiences. Highlighting your teamwork skills will show that you're a good fit for their collaborative culture.
✨Show Enthusiasm for Career Development
The company offers excellent opportunities for career growth, so express your eagerness to develop within the role. Discuss any relevant qualifications, like a Six Sigma Green Belt, and how they have helped you in your career. This will convey that you're not just looking for a job, but a place to grow.