Regulatory Affairs & Medical Devices Expert

Stevanato Group; Padova; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading medical device company in Italy is seeking a Regulatory & Scientific Affairs Specialist. The candidate will manage regulatory processes, prepare documentation, and ensure compliance with standards in the healthcare industry. Candidates should have 2-5 years of experience in regulatory affairs or quality assurance in pharmaceuticals or medical devices, along with a Technical Master Degree. Join a dynamic team dedicated to excellence.

Competenze

• 2-5 years of experience within pharmaceutical or medical device industries.
• Knowledge of ISO, cGMPs, FDA regulations.
• Familiarity with methodologies for risk management.

Mansioni

• Execute regulatory affairs strategy and provide feedback.
• Prepare required documents for regulatory submissions.
• Maintain regulatory files ensuring compliance with standards.

Conoscenze

Regulatory affairs knowledge

Risk management knowledge

Project management skills

Formazione

Technical Master Degree

Descrizione del lavoro

A leading medical device company in Italy is seeking a Regulatory & Scientific Affairs Specialist. The candidate will manage regulatory processes, prepare documentation, and ensure compliance with standards in the healthcare industry. Candidates should have 2-5 years of experience in regulatory affairs or quality assurance in pharmaceuticals or medical devices, along with a Technical Master Degree. Join a dynamic team dedicated to excellence.