
Senior Associate
2 weeks ago
Location : Bangalore, Karnataka
Experience Level : Mid-Senior level
- Ensure SaMD product conformity in accordance with Wysa's QMS before release.
- Create and maintain technical documentation and declarations of conformity.
- Oversee and maintain post-market surveillance and vigilance reporting.
- Serve as the primary liaison with regulatory bodies on submissions, feedback, and incident notifications.
- Manage device labeling, advertising claims, and technical content for compliance.
- Drive regulatory strategy across EU MDR, UK MDR, and US FDA frameworks.
- Maintain compliance with international standards and their applicability.
- Own the effectiveness of internal and external quality processes.
- Lead clinical evaluation and post-market surveillance activities.
- Support SDLC process compliance in collaboration with product and tech teams.
- Implement and manage QMS, including audits (internal/external), CAPA processes, and non-conformances.
- Conduct company-wide training on regulatory procedures and track compliance coverage.
- Coordinate with external medical devices and allied consultants, notified bodies, and global teams.
- Establish dashboards and reporting metrics for senior management.
Qualifications & Skills:
- Minimum bachelor's qualification in any of engineering, science, law, medicine, pharmacy.
- 4 to 6 years of professional experience in regulatory affairs and in QMS of SaMD/AiaMD.
- At least managed one end-to-end QMS to medical device certification of an SaMD device.
- Experience with standards- ISO 13485, IEC 82304/62304, ISO 14971, Usability engineering, 21 CFR 820.
- Ability to learn quickly, work independently, and maintain professional skepticism.
- Ability to work in a fast paced or rapidly changing environment.
- Highly organized and detailed-oriented.
- Excellent collaborator and communicator.
- Excellent analytical and writing skills.
- Proficiency in MS Office and Google workspace.
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