Job Details

ID #50057694
Estado Illinois
Ciudad Cary
Full-time
Salario USD TBD TBD
Fuente Actalent
Showed 2023-06-08
Fecha 2023-06-08
Fecha tope 2023-08-07
Categoría Etcétera
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Regulatory Affairs Specialist ( Medical Device)

Illinois, Cary, 60013 Cary USA

Vacancy caducado!

Seeking a Medical Device Regulatory Affairs Specialist

Co-ordinates and prepares document packages for regulatory submissions from all areas of the organization.

Collects all materials required in submissions, license renewal, and annual registrations.

Keeps abreast of regulatory procedures and changes.

May interact with regulatory agencies.

Works on problems of complex scope where data analysis requires evaluation of specific factors.

Utilizes independent judgment within broad parameters to determine an appropriate solution.

May determine methods and procedures on new projects and may provide guidance to other lower-level staff.

This is an individual contributor role that requires the use of judgement in applying professional expertise and is expected to work independently with minimal supervision.

Experience Level:Expert LevelAbout Actalent: Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Vacancy caducado!

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