This position is responsible for leading Quality Assurance and Quality Engineering activities throughout the Software Development Lifecycle for new product development initiatives and for automated data processing systems used as part of the quality system.
Requirements
- Lead Design Control and Software Development initiatives to develop appropriate Design History File documents for FDA Class II and Class III medical devices, mobile applications, cloud-based systems, and cybersecurity.
- Ensures compliance to IEC 62304, and FDA Guidance on Software Contained in a 510(k) Submission.
- Support efforts for cybersecurity risk management for both US and Rest of World (ROW) requirements.
- Support development teams on the validation of software tools.
- Provide guidance for the generation, review, and approval of design control documentation with primary focus on software development deliverables.
- Collaborate with Project Management to support the Design Control process and Continuous Improvement initiatives to optimize our SW Development processes.
- Serve as the Design Control expert to software development organization.
- Develop and deliver Design Control training for the software development organization.
- Provide expertise in establishing good software requirements, specifications, detailed design, verification and validation protocols and planning documentation.
- Review requirements, specifications, product design documents, validation protocols, test plans, test cases, and other documentation as required and provide timely feedback.
- Support creation of necessary documentation to comply with regulatory requirements and industry best practices.
- Support execution of Risk Management Activities for complex systems in compliance with ISO14971 and software risk requirements in IEC 62304
Benefits
- Medical, dental, and vision insurance
- 401(k) with company match
- Paid time off (PTO)
- And additional employee wellness programs