With innovative products for coloproctology, urology and urogynecology, we improve medical care worldwide. To strengthen our team at the A.M.I. headquarters in Feldkirch, we are looking for a motivated personality in the field of Regulatory Affairs / International Product Approval.
Responsibilities
Preparation and submission of marketing authorisation dossiers to European authorities
Coordination and management of international approval processes
Contact person for regulatory authorities and international distributors
Analysis of country-specific regulatory requirements and derivation of appropriate measures
Ensuring regulatory compliance of products, labels, and documentation
Qualifications
University degree in medical technology, natural sciences or similar
Care and accuracy in texts and documents
Ability to prioritize tasks independently
Very good written and spoken English skills
Ideally, professional experience in the areas of regulatory affairs, international approval procedures, quality management or a comparable field.
Benefits
Company canteen
In-house childcare
Varied area of responsibility with great creative freedom
#J-18808-Ljbffr
Responsibilities
Preparation and submission of marketing authorisation dossiers to European authorities
Coordination and management of international approval processes
Contact person for regulatory authorities and international distributors
Analysis of country-specific regulatory requirements and derivation of appropriate measures
Ensuring regulatory compliance of products, labels, and documentation
Qualifications
University degree in medical technology, natural sciences or similar
Care and accuracy in texts and documents
Ability to prioritize tasks independently
Very good written and spoken English skills
Ideally, professional experience in the areas of regulatory affairs, international approval procedures, quality management or a comparable field.
Benefits
Company canteen
In-house childcare
Varied area of responsibility with great creative freedom
#J-18808-Ljbffr
