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ANGELO DI PERNA

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Last update: 26.08.2019

Regulatory Affairs, Quality Assurance, Sterility Assurance Consultant Medical Device industry

Graduation: Engineer
Hourly-/Daily rates: show
Languages: English (Full Professional) | Italian (Native or Bilingual)

Attachments

cv-eng.pdf

Skills

Engineer with more than 15 years of work experience within the medical device industry, working in international environments and dealing with a variety of devices.
Highly versatile, thanks to the extensive background in RA, QA/QM, Sterilization, Validation and Production, able to manage complex projects and timelines also in complex matrix organizations.
Reliable and meticulous hands-on professional, with solid technical skills and a very cross-functional approach; able to effectively manage time and resources but also to work independently with a minimum control.

Project history

QUALITY ENGINEERING RISK MANAGEMENT CONTRACTOR - Beckton & Dickinson (legacy BARD Angiomed) - Ettlingen (DE)
MANAGER REGULATORY AFFAIRS EMEA - Baxter Healthcare Ltd – Marsa (MT)
REGULATORY AFFAIRS CE MARKING - Baxter Deutschland GmbH – Unterschleissheim (DE)
INTERIM STERILIZATION MANAGER - Optimed GmbH – Ettlingen (DE)
REGULATORY AFFAIRS / QUALITY and STERILIZATION MANAGER - IMeSI – Catania (IT)
STERILIZATION SPECIALIST - IMeSI – Catania (IT)
QA/RA SPECIALIST & VALIDATION ENGINEER - IMeSI – Catania (IT)

Local Availability

Only available in these countries: Malta
Available to travel for medium periods.
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