Engineer - Degreed IV

Engineer - Degreed IV#26-14148 $57.18-$60.24 per hour Pleasanton, CA All On-site Job Description Our Client, a Medical Device and Healthcare company, is looking for a Engineer - Degreed IV for their Pleasanton, CA location.

Responsibilities:

Plan and execute migration of requirements and related data from legacy tools (e.g., DOORS, Jama, Excel, Jira) into new platforms, ensuring data integrity, traceability, and compliance. Administer, configure, and maintain enterprise requirements management tools, including hierarchies, templates, workflows, versioning, and baselining in alignment with the quality system. Develop and maintain a requirements management plan in collaboration with cross functional teams, defining the overall requirements structure and links to associated design control documents. Create and maintain standardized requirements templates, traceability frameworks, and governance models based on quality and regulatory requirements. Maintain the requirements database, develop scripts or automation as needed, and support integrations or add in tools to improve usability and efficiency. Provide training, documentation, and ongoing support to engineers, serving as the primary functional expert for requirements tools and best practices.

Requirements:

Bachelor's degree in Engineering, Computer Science, Biomedical Engineering, or a related discipline for requirements management. A minimum of 5 years with hands on experience administering or configuring enterprise requirements management tools to support regulated development environments (e.g., Codebeamer, DOORS, Jama, or comparable platforms). Ability to quickly learn and adopt new tools is expected. Hands on experience with requirements migration from legacy tools. Strong understanding of medical device product development and design control principles. Excellent verbal and written communication skills, with the ability to train and support engineers at all levels. Ability to work effectively in a collaborative environment. Experience acting as a tool administrator, configuration owner, or advanced power user in a regulated development environment. Experience defining or scaling requirements management frameworks for large or multi team programs. Familiarity with medical device development (FDA 21 CFR Part 820) with the ability to configure tools to support compliant workflows. Experience supporting software driven, connected, or mobile medical devices. Experience with different requirements management or lifecycle tools is valued; strong foundational understanding of requirements structures and traceability is more important than experience with a specific platform. Client Heart Failure division is seeking a Requirements Tools Engineer to support medical device development by enabling and maintaining enterprise requirements management infrastructure. The role focuses on administering, configuring, and optimizing requirements tools, migrating data from legacy systems (e.g., DOORS, Jama, Excel, Jira), and ensuring data integrity, traceability, and regulatory compliance. The engineer collaborates with cross functional teams to define scalable requirements structures, templates, workflows, versioning, and baselining aligned with quality systems. Responsibilities also include developing requirements management plans, maintaining databases, supporting integrations or automation, and acting as the functional expert through training and ongoing support. The role requires 5+ years of hands on experience with enterprise requirements tools in regulated environments, strong knowledge of medical device design controls, and excellent communication skills. Experience with

FDA 21 CFR

Part 820, large scale programs, and software driven medical devices is preferred. Enterprise requirements management tooling: Ability to administer, configure, and maintain tools such as Code beamer, DOORS, or Jama, including hierarchies, workflows, versioning, and baselining. Skill in migrating requirements and related artifacts from legacy tools (e.g., DOORS, Excel, Jira) while preserving traceability and compliance. Design control & regulatory compliance: Strong understanding of medical device design controls and quality systems, including configuring tools to support compliant development processes. ICONMA is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to any status protected by applicable law.