Staff Engineer Regulatory & Quality
Job title: Staff Engineer Regulatory & Quality in San Francisco, CA at Hinge Health
Company: Hinge Health
Job description: Job Description:About the RoleThe Staff Engineer Regulatory & Quality role at Hinge Health is a high-impact position that ensures our cutting-edge medical devices meet global regulatory and quality standards. In this dynamic role, you will spearhead the development, implementation, and maintenance of robust quality assurance programs. You will also manage regulatory submissions and audits, working closely with both internal teams and external regulatory bodies to support product development and lifecycle management. This includes direct collaboration with regulatory agencies. The ideal candidate will possess excellent project management skills and thrive in a collaborative environment, driving innovation and compliance to deliver top-tier medical solutions.What You’ll AccomplishRegulatory Affairs:
Expected salary: $144000 - 216000 per year
Location: San Francisco, CA
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Company: Hinge Health
Job description: Job Description:About the RoleThe Staff Engineer Regulatory & Quality role at Hinge Health is a high-impact position that ensures our cutting-edge medical devices meet global regulatory and quality standards. In this dynamic role, you will spearhead the development, implementation, and maintenance of robust quality assurance programs. You will also manage regulatory submissions and audits, working closely with both internal teams and external regulatory bodies to support product development and lifecycle management. This includes direct collaboration with regulatory agencies. The ideal candidate will possess excellent project management skills and thrive in a collaborative environment, driving innovation and compliance to deliver top-tier medical solutions.What You’ll AccomplishRegulatory Affairs:
- Develop and implement regulatory strategies to achieve timely product approvals in target markets (e.g., FDA, MDR, etc.)
- Prepare, review, and submit regulatory documentation including 510(k), CE marking, and other global submissions
- Maintain up-to-date knowledge of regulatory requirements for medical devices
- Interface with regulatory authorities during audits, inspections, and inquiries
- Collaborate with R&D, engineering, and manufacturing teams to ensure product designs meet regulatory requirements
- Develop, implement, and maintain Quality Management System (QMS) compliant with ISO 13485and other relevant standards
- Oversee internal and external audits to ensure compliance
- Manage CAPA (Corrective and Preventive Actions) processes to resolve product quality issues
- Establish and maintain document control procedures to manage records effectively
- Develop training programs to ensure staff understanding of quality and regulatory requirements
- Bachelor’s degree (or equivalent) in Engineering, Life Sciences or related field
- 8+ years of professional experience in regulatory affairs and/or quality assurance
- Professional experience with FDA, EU MDR, ISO 13485 or other international medical device regulations
- RAC (Regulatory Affairs Certification) or similar credential.
- Proficient technical writing and documentation skills
Expected salary: $144000 - 216000 per year
Location: San Francisco, CA
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