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# Senior Developer

- **Company:** HCL Technologies
- **Location:** Tampa, FL, United States
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Computer-Aided Design, Agile Methodology, Software Quality, Cyber Security, Software Design Documents, Failure Mode Effects Analysis, Internet Security, Scrum Methodology, Software Product Management, Systems Development Life Cycle, Software Engineering, Information Technology
- **Published:** October 31, 2026
- **Apply:** https://www.careerbuilder.com/job-details/senior-developer-tampa-fl--24106ebe-0c3b-40fd-87f1-782ebb62f221

## About the Role

Medical Equipment, Software Development Lifecycle (SDLC), Quality Management, Scrum Project Management and Software Development, Agile Programming Methodologies, Failure Mode and Effects Analysis (FMEA), Quality Engineering, Internet Security, Risk Analysis, Corrective and Preventative Action (CAPA) Systems, * 2-3years of product software experience in Medical devices domain

 * Experience in drafting Software based QMS procedures & work instructions (including third party softwares).
 * Strong knowledge of SDLC, software quality, and quality management systems.
 * Experience working in Agile/Scrum environments and knowledge of SDLC methodologies
 * Lead quality engineering activities, including Software risk assessments (RMF, FMEA, Cybersecurity) and Quality plan execution.
 * Manage CAPA investigations, root cause analysis, corrective actions, and effectiveness monitoring.
 * Review and approve requirements, design documents, test protocols, test results, and change requests.

Key Responsibilities

Role: Software Quality Engineer

 * 2-3years of product software experience in Medical devices domain
 * Experience in drafting Software based QMS procedures & work instructions (including third party softwares).
 * Strong knowledge of SDLC, software quality, and quality management systems.
 * Experience working in Agile/Scrum environments and knowledge of SDLC methodologies
 * Lead quality engineering activities, including Software risk assessments (RMF, FMEA, Cybersecurity) and Quality plan execution.
 * Manage CAPA investigations, root cause analysis, corrective actions, and effectiveness monitoring.
 * Review and approve requirements, design documents, test protocols, test results, and change requests.

Skill Requirements

 * 2-3years of product software experience in Medical devices domain
 * Experience in drafting Software based QMS procedures & work instructions (including third party softwares).
 * Strong knowledge of SDLC, software quality, and quality management systems.
 * Experience working in Agile/Scrum environments and knowledge of SDLC methodologies
 * Lead quality engineering activities, including Software risk assessments (RMF, FMEA, Cybersecurity) and Quality plan execution.
 * Manage CAPA investigations, root cause analysis, corrective actions, and effectiveness monitoring.
 * Review and approve requirements, design documents, test protocols, test results, and change requests.

Other Requirements

Bachelor's degree in Computer science, Software Engineering or related field