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Regulatory consultant

The successful candidate will be responsible for:

  • Consultancy in the biomedical regulatory field (MDR 2017/745, FDA Guidance), pharmaceutical, substance-based medical devices, diagnostics and cosmetics

The ideal candidate has the following requisites:

  • Scientific degree, preferably: CTF, Pharmacy, Medical/Pharmaceutical Biotechnology, Biology, Biomedical Engineering

  • Knowledge of CE marking

  • Ability to draw up BEP and BER Plans, Toxicological Assessments, Gap Analysis, Justifying Rationales, Technical Files, Risk Analysis, Clinical Evaluation, Post Market Surveillance, Data Analysis and Data Mining

  • Knowledge of English (good written and spoken level)

  • Experience: minimum 1 year, preferably 2 years

The profile is completed by:

  • Specialization in Toxicology

  • Plus: registration in the register

Location and working hours:

Zola Predosa (BO)
Full Time

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