Sr Eng RD Soft Eng

Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position has the following responsibilities:

• Support the design, development and testing of Medical Device Software, including Software as a Medical Device (SaMD) products.
• Provide leadership, guidance and expertise on the software development process, procedures and practices
• Partner with R&D to refine requirements, and to ensure that architecture/ design documents are comprehensive.
• Facilitate the documentation and tracking of verification activities, including code review findings.
• Review test case execution results and manage defects.
• Facilitate software risk assessment sessions and own the development of risk documents.
• Support regulatory filings and registrations.
• Support internal and external audits or inspections of SaMD products and processes and own Non-conformances or CAPAs and drive root cause investigations.
• Provide technical support for audits of software suppliers and software consultants.
• Conduct training on Medical Device Software development processes and quality systems.
• Train and mentor new engineers and lower-level quality engineers.
• Provide expertise in applicable industry standards and regulations including, but not limited to as IEC 62304, FDA guidance, FDA Part 11, ISO13485, EU MDR, ISO14971, IEC 62366, ISO 27001, and HIPAA.
• Provide guidance to project teams, suppliers and other disciplines to ensure compliance with company policies and procedures, as well as medical device regulations.
• Ensure that patient's ePHI and PII data is protected and security requirements are met.
• Know, understand, incorporate and comply with all applicable laws and regulations relating to DePuy Synthes business activities and Policies and Procedures for Health Care Compliance Program and Code of Conduct.

Additionally: o Responsible for communicating business related issues or opportunities to next management level o Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable. o For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable o Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures o Performs other duties assigned as needed

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• Ability to work in a team and demonstrate good interpersonal, organizational, and verbal/written communications skills.
• Extensive use of the personal computer and associated work tools (Word, Excel, Power Point) is required.
• Medical device industry experience.
• ASQ Certification as a Software Quality Engineer, or equivalent, is preferred.

• This position reports to the Manager or Senior Manager of Quality Engineering · Potential internal interfaces that this role may encounter include:o Interfacing with other Quality Team memberso Working with Research & Development on product issueso Working with Product Owners on product requirementso Working with Program Management on product scheduleso Working with other product teams to support other products or platformso Working with other supporting teams such as Product Security, Regulatory Affairs, Medical Affairs, Medical Safety, Customer Support, Product Complaints, Privacy, Legal, Independent Reviewers, etc. for review and approval of design history file (DHF) documentation