Job TitleRegulatory Affairs Specialist Job Description Your role: Develop global regulatory strategies for software medical devices ensuring ongoing compliance throughout the product lifecycle. Prepare and manage regulatory submissions and approvals in the US, Europe, and Canada. Represent Regulatory
Company Overview Verathon is a global medical device company focused on supporting customers by being their trusted partner, delivering high-quality products that endure over time and ensure clinical and economic utility. Two areas where Verathon has significantly impacted
We are seeking a hands‑on HR Business Partner to join our European HR team, supporting a rapidly growing medical device organization with approximately 200+ employees across multiple countries. This role goes beyond traditional HR BP responsibilities — you