Requirements Tools Engineer

Position Title: Requirements Tools Engineer

Work Location: Pleasanton, CA (Onsite)

Assignment Duration: 12 months (possibility of extension)

Position Summary:

The Requirements Tools Engineer will be responsible for enabling and supporting requirements management infrastructure for medical device product development programs. This role is focused on administering and configuring enterprise requirements management platforms, supporting data migration activities, and enabling engineering teams through processes, and training.

Working in Pleasanton, CA, this individual will collaborate with cross-functional engineering teams to establish scalable structures and best practices that allow engineers to efficiently create and manage requirements and other design control documents in the management tool.

Key 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.

Qualification & Experience:

* 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).

* 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.

Additional Information:

Only one interview - Video conference (Onsite if candidate is local)