At a Glance
- Tasks: Lead global regulatory compliance for medical devices and collaborate with cross-functional teams.
- Company: Join KARL STORZ, a mission-driven leader in MedTech innovation.
- Benefits: Enjoy a hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Gain exposure to FDA, EU MDR, and international submissions in a dynamic environment.
- Why this job: Make a real impact on product safety and compliance in the medical device industry.
- Qualifications: Experience in regulatory affairs and strong collaboration skills are essential.
The predicted salary is between 63000 - 77000 £ per year.
KARL STORZ seeks a Regulatory Intelligence Manager to lead global regulatory compliance across the medical device lifecycle.
You’ll partner with Engineering, Quality, Product Management and Regulatory Affairs to ensure safe, compliant products from concept to commercialization.
This hybrid role blends hands-on regulatory work with cross-functional collaboration, offering exposure to FDA, EU MDR, ISO 13485, and international submissions in a global, mission-driven Med Tech environment.
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Hybrid Regulatory Intelligence Lead for Medical Devices in Charlton employer: カールストルツ・エンドスコピー・ジャパン（株）
KARL STORZ is an exceptional employer that fosters a collaborative and innovative work culture, where employees are empowered to make meaningful contributions to medical technology. With a commitment to employee growth and development, the company offers opportunities for professional advancement while maintaining a strong focus on safety and quality. Located in Charlton, MA, the hybrid work model allows for flexibility, ensuring a healthy work-life balance as you join a family-owned business dedicated to improving patient care worldwide.
