At a Glance
- Tasks: Ensure quality and regulatory compliance for medical devices while maintaining ISO 13485 standards.
- Company: Join X4 Life Sciences, a leader in the medical device industry.
- Benefits: Permanent position with opportunities for professional growth and development.
- Other info: Autonomous role with minimal supervision in a dynamic team environment.
- Why this job: Make a difference in healthcare by ensuring the safety and quality of medical devices.
- Qualifications: 3-4+ years in medical device QA/regulatory roles with strong CAPA/NCR experience.
The predicted salary is between 35000 - 42000 £ per year.
X4 Life Sciences in the United Kingdom is seeking a Quality and Regulatory Co-Ordinator to join their medical device team on a permanent basis. This hands-on, autonomous role focuses on maintaining the ISO 13485 QMS and ensuring regulatory compliance across MDR/UKCA activities.
The ideal candidate has 3–4+ years in a medical device QA/regulatory role, strong CAPA/NCR experience, and proven ability to manage documents, audits, and training records with minimal supervision.
#J-18808-LjbffrMedical Device Quality & Regulatory Specialist in Essex employer: X4 Life Sciences
X4 Life Sciences is an exceptional employer, offering a dynamic work environment where creativity and collaboration thrive. With a strong focus on employee growth, the company provides ample opportunities for professional development within the healthcare communications sector, alongside a competitive benefits package that includes a pension and annual bonus. Located in a vibrant area, the hybrid working arrangements allow for a balanced work-life experience, making it an ideal place for those seeking meaningful and rewarding employment.
