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Freelance Regulatory Affairs Consultant - IVD Expert

Freelance Regulatory Affairs Consultant - IVD Expert

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Freelance Regulatory Affairs Consultant - IVD Expert

  • Location:

    New York

  • Sector:

    Medical Device

  • Contact:

    Ryan Goodland

  • Salary:

    Up to US$999 per hour + COMEPTITIVE

  • Job type:

    Interim/Contract

  • Contact email:

    pharmajobs@msigroupltd.com

  • Job ref:

    REG IVD US 2_1601286423

  • Published:

    29 days ago

  • Duration:

    12 months

  • Startdate:

    ASAP

Freelance Regulatory Affairs Consultant - IVD Expert | Remote based (EMEA, APAC or US)

To work for a Medical Device consultancy, responsible for global operations. We are looking for a someone to provide Regulatory Affairs consulting services within the IVD space.

What will you be responsible for?
- Regulatory consulting
- IVDR transition and implementation
- Pre-submission and clinical strategy support
- Clinical Evaluation Plans
- Technical Documents
- Hosting conferences & delivering presentations

Experience?
- Laboratory and/or manufacturing background
- IVD expert (High consultant level)
- IVD Directive (IVDD) to IVD Regulation (IVDR) transition and implementation