- Independent review of an existing BEP (ISO
- Identification of gaps, risks, or over-testing
- Alignment with EU MDR and Notified Body expectations
- Practical recommendations to strengthen CE readiness
- Support during Notified Body review, including responses to questions and deficiencies
- Experience with a) Dermal fillers (ideal) b) Long-term implantable or injectable medical devices (strong preference) c) Experience with polymer-based implants, dental implants, or resorbable membranes (also relevant).
- Experience reviewing or challenging third-party BEPs is a strong advantage.
- Prior direct interaction with Notified Bodies on biocompatibility/ toxicology topics under EU MDR (MDD-only experience is insufficient)
- Hands-on ownership of toxicology strategy (not academic review only) including assessment of degradation products, residual cross-linkers, impurities, and exposure routes
- External consultant
- Hourly, flexible, execution-focused
-
We are seeking an experienced Toxicology expert to join our team in Europe. This is a great opportunity to join a consultancy with strong track record of advising clients in the chemical sector. · Support clients with product registrations, toxicological evaluations, exposure ass ...
Milan A tempo pieno1 mese fa
-
We are seeking an experienced Regulatory Toxicology Crop Protection expert to join our team in Europe. · ...
Milan1 mese fa
- Lavorare in azienda
Regulatory Affairs Project Manager – Plant Protection
Solo per membri registrati
ERM seeks an experienced Plant Protection Regulatory Affairs professional to join as Project Manager in Southern Europe. · Manage all aspects of the regulatory process for active substances and formulations with a focus on biological control registrations. · ...
Milan1 mese fa
Biocompatibility & Toxicology Consultant (BEP Review | EU MDR | Dermal Fillers) - monza - Glyance
Descrizione
Glyance is seeking a senior Biocompatibility & Toxicology Consultant to provide an independent, critical review of an existing Biological Evaluation Plan (BEP) for dermal filler products, as part of an active CE submission under EU MDR.
This is a consulting engagement (hourly / project-based) — not an employment role.
Scope of support includes:
Highly relevant experience includes:
Engagement type:
If you have practical MDR experience and have supported CE submissions for fillers or similar products, we'd be happy to connect.
-
Managing Technical Consultant
A tempo pieno Solo per membri registrati Milan
-
Regulatory Toxicologist Crop Protection
Solo per membri registrati Milan
-
Regulatory Affairs Project Manager – Plant Protection
Solo per membri registrati Milan
