Intellectt Inc

Requirement Tools Engineer

⭐ - Featured Role | Apply direct with Data Freelance Hub
This role is for a Requirements Tools Engineer in Pleasanton, CA, on a W2 contract. Requires a Bachelor's in Engineering or related field, 5+ years with requirements management tools, and experience in medical device design controls.
🌎 - Country
United States
💱 - Currency
$ USD
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💰 - Day rate
Unknown
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🗓️ - Date
June 26, 2026
🕒 - Duration
Unknown
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🏝️ - Location
On-site
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📄 - Contract
W2 Contractor
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🔒 - Security
Unknown
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📍 - Location detailed
Pleasanton, CA
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🧠 - Skills detailed
#Data Integrity #Automation #Scala #Computer Science #Database Maintenance #Compliance #Jira #Migration
Role description
Hiring: Requirements Tools Engineer Location: Pleasanton, CA (Onsite) Employment Type: W2 Contract We are seeking an experienced Requirements Tools Engineer to support medical device product development by administering and optimizing enterprise requirements management tools in a regulated environment. Key Responsibilities: • Administer, configure, and maintain enterprise requirements management tools (Codebeamer, DOORS, Jama, or similar) • Plan and execute migration of requirements and design control data from legacy systems while ensuring traceability and data integrity • Develop and maintain requirements management plans, templates, workflows, versioning, and baselines • Establish scalable requirements structures and traceability frameworks aligned with quality and regulatory standards • Support tool integrations, automation, and database maintenance • Provide training and ongoing support to engineering teams on requirements management best practices Required Qualifications: • Bachelor's degree in Engineering, Computer Science, Biomedical Engineering, or a related field • 5+ years of hands-on experience administering or configuring enterprise requirements management tools • Experience migrating requirements from tools such as DOORS, Jama, Excel, or Jira • Strong understanding of medical device design controls and quality systems • Excellent communication and collaboration skills Preferred Qualifications: • Experience with FDA 21 CFR Part 820 and regulated medical device environments • Experience defining requirements management frameworks for large or multi-team programs • Knowledge of software-driven or connected medical devices • Experience with requirements traceability, governance, and compliance