DescriptionMSPSis looking for a Corrections & Removals (C&R) Specialist to join the front-line team of our client PHILIPS Personal Health Greece & Cyprus collaborating with cross-functional teams and contribute to multiple projects that drive business success.
Are you passionate about quality compliance and making healthcare safer Join the QA Europe Region team and play a critical role in ensuring patient safety and regulatory excellence across medical devices in the market.
This is your opportunity to work at the intersection of Quality Regulatory Affairs and Post-Market Surveillance collaborating with cross-functional teams across Europe to drive corrective actions that truly matter.
Key Responsibilities
- Support the execution of Corrections & Removals strategies across the region
- Ensure timely reporting and closure of Field Safety Corrective Actions (FSCAs)
- Coordinate customer notifications and due diligence activities
- Maintain C&R documentation and regulatory records
- Monitor KPIs and escalate risks proactively
- Support responses to regulatory authority inquiries
- Contribute to continuous improvement of the C&R process
- Your work will directly contribute to product quality compliance with EU MDR regulations and customer trust.
Qualifications & Skills
- Bachelors degree in Business Administration Marketing Life Sciences or a related field
- Excellent written and verbal communication skills in Greek and English
- 1 year experience in Quality Regulatory Affairs or medical device industry
- Strong organizational and analytical skills with attention to detail
- Ability to manage multiple priorities and deadlines
- Knowledge of EU MDR (Regulation (EU) 2017/745) and ISO 13485 is a plus
- Reliability structure and accountability
- Team-oriented personality with strong communication skills
What We Offer
- A dynamic work environment in the growing medtech industry
- Continuous learning and professional development opportunities
- Collaboration with cross-functional teams
- Competitive compensation package
If you are motivated to grow within a commercial support role in the medical technology field we would be glad to receive your application.
Required Experience:
IC
DescriptionMSPSis looking for a Corrections & Removals (C&R) Specialist to join the front-line team of our client PHILIPS Personal Health Greece & Cyprus collaborating with cross-functional teams and contribute to multiple projects that drive business success.Are you passionate about quality compli...
DescriptionMSPSis looking for a Corrections & Removals (C&R) Specialist to join the front-line team of our client PHILIPS Personal Health Greece & Cyprus collaborating with cross-functional teams and contribute to multiple projects that drive business success.
Are you passionate about quality compliance and making healthcare safer Join the QA Europe Region team and play a critical role in ensuring patient safety and regulatory excellence across medical devices in the market.
This is your opportunity to work at the intersection of Quality Regulatory Affairs and Post-Market Surveillance collaborating with cross-functional teams across Europe to drive corrective actions that truly matter.
Key Responsibilities
- Support the execution of Corrections & Removals strategies across the region
- Ensure timely reporting and closure of Field Safety Corrective Actions (FSCAs)
- Coordinate customer notifications and due diligence activities
- Maintain C&R documentation and regulatory records
- Monitor KPIs and escalate risks proactively
- Support responses to regulatory authority inquiries
- Contribute to continuous improvement of the C&R process
- Your work will directly contribute to product quality compliance with EU MDR regulations and customer trust.
Qualifications & Skills
- Bachelors degree in Business Administration Marketing Life Sciences or a related field
- Excellent written and verbal communication skills in Greek and English
- 1 year experience in Quality Regulatory Affairs or medical device industry
- Strong organizational and analytical skills with attention to detail
- Ability to manage multiple priorities and deadlines
- Knowledge of EU MDR (Regulation (EU) 2017/745) and ISO 13485 is a plus
- Reliability structure and accountability
- Team-oriented personality with strong communication skills
What We Offer
- A dynamic work environment in the growing medtech industry
- Continuous learning and professional development opportunities
- Collaboration with cross-functional teams
- Competitive compensation package
If you are motivated to grow within a commercial support role in the medical technology field we would be glad to receive your application.
Required Experience:
IC
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