Ophthalmic Medical Safety & Vigilance Lead

Ophthalmic Medical Safety & Vigilance Lead

Full-Time 40000 - 50000 Β£ / year (est.) No working from home possible
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At a Glance

  • Tasks: Provide expert ophthalmic assessments and manage clinical safety evaluations.
  • Company: Global medical device client with a focus on innovation and compliance.
  • Benefits: Competitive salary, professional development, and a chance to impact patient safety.
  • Other info: Opportunity to work in a dynamic environment with global impact.
  • Why this job: Join a leading company and ensure the safety of innovative contact lens products.
  • Qualifications: Licensed Ophthalmologist with experience in clinical safety and regulatory compliance.

The predicted salary is between 40000 - 50000 Β£ per year.

Lenn Tech Search is partnering with a global medical device client seeking a licensed Ophthalmologist.

This role involves providing expert ophthalmic assessments of adverse events and supporting compliance for UK/EU/global vigilance obligations.

The successful candidate will manage clinical safety evaluations and enhance clinical evidence related to the product portfolio of diverse contact lenses while ensuring the safety and integrity of trials and regulatory compliance.

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Ophthalmic Medical Safety & Vigilance Lead employer: LennTech Search

Join a dynamic and innovative medical device company that prioritises quality and compliance, offering a collaborative work culture where your expertise as a Quality Systems Specialist will be valued. With a strong focus on employee development, you will have access to continuous training opportunities and the chance to make a significant impact in a fast-paced environment. Located in a thriving area, this role not only provides competitive benefits but also fosters a sense of community and purpose in improving healthcare outcomes.

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Contact Details:

LennTech Search Recruitment Team

We think you need these skills to ace Ophthalmic Medical Safety & Vigilance Lead

Ophthalmic Assessments
Clinical Safety Evaluations
Regulatory Compliance
Adverse Event Management
Clinical Evidence Enhancement
Product Portfolio Management
Trial Safety and Integrity