Medical Device Regulatory Coordinator
7 giorni fa
Regulatory Affairs Specialist Opportunity
Cosmo Intelligent Medical Devices is seeking an entry-level Regulatory Affairs Specialist to join our team. In this role, you will be responsible for ensuring compliance with applicable regulations, guidelines, and standards.
Responsibilities:
- Assess, prepare, and manage technical documentation to support certification and submission processes.
- Prepare and manage technical dossiers for submission in other countries according to local regulations and guidance documents.
- Collaborate with cross-functional teams to develop and maintain technical documentation.
Qualifications:
- Bachelor's degree in engineering, science, or related scientific discipline, or equivalent.
- English proficiency at a professional level.
- Knowledge of regulatory frameworks, such as EU Regulation 2017/745 and Title 21 CFR parts 800-898.
Why Join Us:
Cosmo Intelligent Medical Devices offers a dynamic and innovative work environment, competitive compensation, and opportunities for growth and development.
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