Senior Software DQA Engineer

4 weeks ago

Acton, Massachusetts, United States Insulet Corporation Full time
Job Description

Insulet Corporation is seeking a highly motivated and experienced Senior Software DQA Engineer to join our team. As a key member of our software development team, you will be 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.

This role will interface with other Insulet departments (e.g. Sr. Management, Operations, and Information Technology, Engineering, New Business Development and Regulatory Affairs) as well as other external parties on issues related to product development, launched product support, and software used for automation of the quality system.

The ability to effectively communicate software and design and development regulations, optimize the development process, and ensure ambiguities and conflicting requirements are resolved are critical to the success of the position.

Responsibilities:
  • 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.
  • Ensure 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.
  • 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 and optimize the Design Control and SW Development Processes.
  • Serve as the Design Control expert to software development organization.
  • Develop and deliver Design Control training for the software development organization.
  • Support development teams on the validation of software tools.
  • Work with software, hardware, user experience, marketing, manufacturing, and quality assurance on generation, documentation, verification and validation of requirements.
  • Assist with the execution of validation testing for computerized systems that are used as part of production processes or in the quality system.
  • Lead creation of necessary documentation to comply with regulatory requirements and industry best practices.
  • Lead Risk Management Activities for complex systems in compliance with ISO14971 and software risk requirements in IEC 62304.
  • Establish and maintain software quality assurance programs, processes, procedures and controls to ensure compliance with FDA regulations and established standards such as IEC 62304
  • Provide expertise in establishing good software requirements, specifications, detailed design, verification and validation protocols and planning documentation
  • Provide guidance on, and participate in software development activities including design and code reviews, requirements analysis and tracing, defect tracking and configuration management
  • Review requirements, specifications, product design documents, validation protocols, test plans, test cases, and other documentation as required and provide timely feedback.
  • Applies a good working knowledge of Software Development Life Cycle (IEC 62304), Design Controls (ISO and other regulatory requirements and agencies as it relates to Quality Assurance activities in software development.
  • Maintain effective communication with the project software engineers to make sure that user needs, requirements, plans, verification and validation documents, risk assessments, and other documentation is complete.
Minimum Requirements:
  • ASQ, CSQE or other software quality certificates are beneficial.
  • BS degree, in an engineering/scientific/computer systems or quality management curriculum or equivalent experience. Master's degree preferred.
  • Experience with medical device software development.
  • Experience with a risk-based approach to validate computerized systems, Commercial off the Shelf (COTS) software and SW Tools.
  • Experience with software mobile applications, cloud-based systems, and cybersecurity.
  • A minimum of 5 years' work experience in Software Quality Engineering within an FDA, ISO or other regulated environment and/or equivalent combination of education and experience.
  • Experience in the development and implementation of effective Design Control Systems.
  • Working knowledge of the Quality System Regulation (FDA 21 CFR Part 820) and ISO 13485 quality system standards.
  • Working knowledge of IEC 62304, ISO 14971, IEC 62366, IEC 60601, and FDA guidance documents on software development, cybersecurity, and submission requirements for PMA and 510(k).
  • Demonstrated experience organizing and maintaining large documentation sets.
  • Experience with structured phase-gate product development processes.
  • Familiarity with GAMP 5 guidance.
  • Experience with software design V&V, computerized systems validations, and process validations.
  • Familiarity with various software development tools (e.g. configuration management, issue/defect tracking, requirements analysis, etc.).
  • Experience with software development lifecycles with emphasis on the software quality engineering aspects.
Skills/Competencies:
  • Effective verbal and written communication skills.
  • Experience collaborating and communicate with individuals at multiple levels in an organization.
  • Ability to prioritize and manage critical project timelines in a fast-paced environment. Must be able to handle multiple responsibilities concurrently.
  • Strong analytical and problem-solving skills.
  • Able to work effectively in a high-stress, high-energy environment.
  • Ability to manage people and projects in a fast-moving environment.

At Insulet Corporation, we are committed to providing a work environment that is inclusive, respectful, and free from discrimination. We are an equal opportunity employer and welcome applications from diverse candidates.

Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits.

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