Software QARA Consultant in Slough

Software QARA Consultant in Slough

Slough Full-Time 50000 - 60000 € / year (est.) No home office possible
Computer Futures

At a Glance

  • Tasks: Lead quality and regulatory activities for innovative medical software projects.
  • Company: Join a forward-thinking company focused on SaMD and AIaMD solutions.
  • Benefits: Flexible remote work, competitive pay, and the chance to shape healthcare technology.
  • Other info: Short-term contract with potential for future opportunities in a dynamic field.
  • Why this job: Make a real difference in healthcare by ensuring software meets high standards.
  • Qualifications: Experience with CE marked & FDA-authorised products and knowledge of ISO 13485.

The predicted salary is between 50000 - 60000 € per year.

We're seeking an experienced QARA Consultant to work on multiple SaMD and AIaMD projects on quality and regulatory activities. You'll own end-to-end regulatory submissions (CE & FDA), support QMS implementation.

Key requirements:

  • Proven experience with CE marked & FDA-authorised SaMD/AIaMD products
  • Strong knowledge of ISO 13485

Software QARA Consultant in Slough employer: Computer Futures

As a leading player in the Software as Medical Device sector, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to excel. With a strong focus on professional development, we offer numerous growth opportunities and the flexibility of remote work, allowing you to balance your career with personal commitments while contributing to impactful projects in the healthcare technology space.

Computer Futures

Contact Detail:

Computer Futures Recruiting Team

StudySmarter Expert Advice🤫

We think this is how you could land Software QARA Consultant in Slough

Tip Number 1

Network like a pro! Reach out to your connections in the medical device field and let them know you're on the lookout for opportunities. You never know who might have a lead on a QARA Consultant role that’s perfect for you.

Tip Number 2

Get your online presence sorted! Make sure your LinkedIn profile is up-to-date and showcases your experience with CE marked and FDA-authorised products. Join relevant groups and engage in discussions to get noticed by potential employers.

Tip Number 3

Prepare for interviews by brushing up on your knowledge of ISO 13485 and regulatory submissions. Be ready to discuss your past projects and how you've successfully navigated quality and regulatory activities in the SaMD space.

Tip Number 4

Don’t forget to apply through our website! We’ve got loads of opportunities that might just be the right fit for you. Plus, applying directly can sometimes give you an edge over other candidates.

We think you need these skills to ace Software QARA Consultant in Slough

Quality Assurance
Regulatory Affairs
ISO 13485
CE Marking
FDA Regulations
QMS Implementation
Experience with SaMD

Some tips for your application 🫡

Tailor Your CV:Make sure your CV highlights your experience with CE marked and FDA-authorised SaMD/AIaMD products. We want to see how your skills align with the role, so don’t be shy about showcasing relevant projects you've worked on!

Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for our QARA Consultant role. Share specific examples of your work in quality and regulatory activities that relate to the job description.

Showcase Your Knowledge:We’re looking for someone with strong knowledge of ISO 13485 and other relevant standards. Make sure to mention any certifications or training you have in these areas, as it’ll help us see your expertise right away.

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 to do!

How to prepare for a job interview at Computer Futures

Know Your Regulations

Make sure you brush up on the specifics of CE marking and FDA authorisation processes. Familiarise yourself with ISO 13485 and any other relevant standards, as this will show your depth of knowledge and commitment to quality in the SaMD and AIaMD space.

Showcase Your Experience

Prepare to discuss your previous projects in detail, especially those involving regulatory submissions. Be ready to share specific examples of challenges you faced and how you overcame them, as this will demonstrate your problem-solving skills and hands-on experience.

Understand the Company’s Focus

Research the company’s recent projects and their approach to QARA in the context of SaMD and AIaMD. This will help you tailor your answers to align with their goals and show that you’re genuinely interested in contributing to their success.

Ask Insightful Questions

Prepare thoughtful questions about the company’s quality management systems and regulatory strategies. This not only shows your interest but also gives you a chance to assess if their working style aligns with your own.