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Post Market R&D team is seeking a highly skilled, experienced, and versatile Software Engineer to maintain and enhance released products and developing innovative, high-quality solutions addressing field, regulatory, cybersecurity, and market needs.
The primary focus of this role is Windows Desktop software development, including applications, tools, services, installers, and utilities for medical products and medical applications.
The ideal candidate brings a strong and broad software engineering background, with a proven ability to contribute across multiple software domains such Web, Cloud , DevOps and CI/CD.
As part of Global company, we provide solutions that helps our patients alleviate pain, restore health, and extend life.
Responsibilities may include the following and other duties may be assigned:
Windows Desktop Software Development: Design, develop, maintain, and enhance Windows-based desktop applications, tools, services, installers, and utilities.
Debugging & Troubleshooting: Diagnose and resolve issues in products and applications.
Cross-Functional Collaboration: Work closely with Hardware, System, QA, and Product teams to meet project goals. Act as the primary technical contact for inquiries and provide ongoing support.
Documentation Management: Create and maintain comprehensive Software Development Lifecycle Documentation, including design and verification documents, complying medical standards.
Security & Compliance: Conduct security assessments and ensure adherence to medical software standards. Maintain SBOMs (Software Bill of Materials)
DevOps & CI/CD: Contribute to DevOps activities, CI/CD pipelines, automation and utilities. Develop automation tools and scripts using Python and PowerShell.

As a Quality Engineer in Manufacturing, you will play a key role in ensuring that products are manufactured in compliance with internal quality standards, regulatory requirements, and our companys commitment to patient safety and product excellence. This position partners closely with Manufacturing, Operations, R&D, and Supply Chain to drive quality improvements and support continuous improvement initiatives on the production floor.
Responsibilities may include the following and other duties may be assigned:
Provide quality engineering support for manufacturing operations and engineering.
Support production, engineering, validation activities including training, reviewing and approving documentation, work instructions, SOPs , supporting risk assessments, to ensure compliance with regulatory and quality system requirements.
Lead and support investigations of nonconformances, deviations, and CAPAs, including root cause analysis and implementation of corrective and preventive actions.
Collaborate with cross-functional teams to identify, assess, and mitigate quality risks in manufacturing processes.
Support internal and external audits, including preparation, participation, and follow-up on audit findings.
Drive continuous improvement initiatives using quality and lean methodologies.
Ensure effective implementation and monitoring of process controls and quality metrics.
Support change management activities ensuring requirements are identified and executed when applicable.
Participate in Management Review and Quality Metrics reporting.