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Strong employer brand, metro location, and broad product leadership requirements increase candidate competition.
High — requires ophthalmic device, regulatory, and ECP workflow expertise, limiting cross-industry transfer.
High — explicit 7–10 years, domain-specific ophthalmic device experience and regulatory expertise required.
Define and own multi-year consultation software strategy focused on device-agnostic, measurement-driven workflows guiding eye care professionals (ECPs).
Oversee product lifecycle from concept through launch and post-launch performance, ensuring regulatory compliance and seamless cross-functional coordination.
Lead and develop a team of Product Managers, manage stakeholder relationships including clinical, regulatory, marketing, and global leadership.
7-10 years of progressive product/category management experience in medical/ophthalmic devices or vision care.
Degree in Computer Science, Biomedical Engineering, or related technical/scientific field; MBA or equivalent is advantageous.
Experience managing global international product launches across multiple regions (EMEA, APAC, Americas) preferred.
Not explicitly mentioned in the JD: notice period or strict location requirements.
Experienced in defining digital workflow solutions for clinical or commercial decision support, especially device-agnostic consultation software in healthcare or retail.
Proficient in regulatory pathways including FDA 510(k), EU MDR, ISO 13485 relevant to ophthalmic devices.
Demonstrated ability to influence senior stakeholders and operate effectively in a global matrix organization with cross-cultural team leadership.