Valtera Group is partnering with an early-stage medical device company to appoint an independent Regulatory Adviser. This is a focused advisory retainer, not a full-time role, suitable for a specialist who can contribute alongside other work.
You’ll confirm design inputs against IEC 60601-1 and related standards, review V&V plans, advise on usability and clinical study protocols, and help with ISO 14971 risk management and ISO 13485 audits. Regular on-site time in the South East is expected.
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Regulatory Advisor (Medical Devices) — 2 Days/Month, Remote in England employer: Consult
At Consult, we pride ourselves on being an exceptional employer that fosters a dynamic and inclusive work culture. Our North America team is dedicated to professional growth, offering robust training and development opportunities while working in a fast-paced, innovative environment. Join us to be part of a collaborative team that values your contributions and supports your career aspirations in the exciting MedTech sector.
