Sentinel Diagnostics, leader in the Development and Production of Diagnostic Kits for Clinical Chemistry, Immunology, Molecular Biology, Chromatography and Rapid Test, in order to expand the Regulatory Affairs Team, is looking for a:
REGULATORY AFFAIRS SPECIALIST
Responsibilities

Definition of regulatory strategies for global market access of In Vitro Diagnostic medical devices, in accordance with the company priorities
Preparation and submission of the mandatory technical and legal documentation files for worldwide product registration approvals, including the European and US markets
Collaboration with distributors Regulatory Affairs functions
Monitoring of the new international applicable requirements in order to support the company business
Continuous maintenance of the products conformity to applicable laws, regulations, guidelines and international standards
Participation in corporate projects in order to provide regulatory guidance to cross-functional teams

Requirements

Scientific Degree
At least 3/4 years of experience in similar role within the Medical Device/IVD sector, possibly in an international context
Excellent knowledge of national and international regulatory regulations (ISO 13485, ISO 9001, MDSAP, IVDR 746/2017, US FDA 21 CFR)
Good knowledge of the regulatory management of In Vitro Diagnostic Medical Devices (IVD)
Any additional knowledge of the regulatory management of In Vitro Diagnostic Medical Devices (MDCG Guidelines, Anvisa, Health Canada, 510K) will be a preferential requirement
Ability to interact with the different teams in the organization
Capacity to meet deadlines and focus on priorities
Proactivity and autonomy
Motivation and enthusiasm

Seniority level

Entry level

Employment type

Full-time

Job function

Other

Industries

Medical Equipment Manufacturing, Pharmaceutical Manufacturing, and Measuring and Control Instrument Manufacturing

Referrals increase your chances of interviewing at Sentinel Diagnostics by 2x
#J-18808-Ljbffr