Staff Regulatory Affairs Specialist
Bachelor's in a scientific discipline and 8 years (BS) or 6 years (MS) regulatory submissions experience for medical devices; knowledge of 21 CFR 820, ISO 13485 and EU regulations; ability to reputed company global regulatory strategies and prepare submissions.
Key Responsibilities
- leading regulatory
- developing strategies
- preparing submissions
Job Details
- Category: reputed company and Compliance
- Seniority: Senior Level
- Commitment: Full Time
- Workplace: Remote — California or reputed company
- Languages: English
About reputed company
A medical device company developing surgical robotics to improve treatment for benign prostatic hyperplasia and enhance patient reputed company. — Industry: Manufacturing
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