EMPREGO PROJECT SPECIALIST REGULATORY AFFAIRS

Senior regulatory specialist, emea regulatory affairs (clinical investigation support)   boston scientific's hybrid workplace includes remote and onsite roles...

About the role:  under minimal supervision, the senior regulatory affairs specialist is responsible for planning, managing, and implementing regulatory submissions...

Job position open: - project manager & senior business developer of regulatory affairs main tasks: - management of regulatory and market access bootcamp project -...

regulatory affairs specialist - maternity cover (2 years)   as a regulatory affairs specialist you will act as the person responsible for regulatory compliance for...

Experience:       minimum 3 years of work experience in a regulatory affairs department within the healthcare sector or pharmaceutical sector...

Fte tipo de oferta: tempo inteiro localização: avepark – parque de ciência e tecnologia, guimarães, portugal... funções: verificação e garantia da conformidade...

We are currently seeking a senior regulatory affairs specialist to join our global regulatory affairs department –   regulatory science   team...  we are a global organisation but...

We are currently seeking a principal regulatory affairs specialist to join our global regulatory affairs department – regulatory science team...

With adequate supervision, the regulatory affairs specialist ii is responsible for planning, managing, and implementing regulatory submissions to the us fda, eu...

Experience: previous internship in regulatory affairs or clinical affairs in medical devices, pharmaceuticals, cosmetics, or other fields would be an advantage...

Support the quality regulatory department (qara), in audits and regulatory inspections... provide regulatory advice and guidance to project teams on regulatory...

With adequate supervision, the regulatory affairs specialist ii is responsible for ensuring continued compliance with regulatory agency approvals through change...

Review, establish and agree on project planning and project timelines... provide local expertise to sams and project team during initial and on-going project timeline...

- basic knowledge of regulatory affairs for medical devices... - communicating effectively with internal and external stakeholders to ensure alignment and timely...

Essential functions • acts as a regulatory team leader on more complex projects, which may include technical writing; • prepares and/or reviews regulatory documentation...

Enters own labeling-related tasks in the iqvia internal project management tool... do you meet the skills, experience, and educational requirements of the role?...

O     conducts searches within commercial regulatory intelligence databases to identify regulations and guidelines relevant for clinical regulatory intelligence...

Responsibilities: - lead and manage multi-regional team in the following areas - monitor new, revised or emerging regulatory requirements from a global to a local...

Job responsibilities gather new regulatory information through routine surveillance of agreed regulatory sources... conduct regular annual country review of regulatory...