Staff Process Engineer/ Quality Systems Engineer - Remote
Job Description
Overview
Staff Process Engineer / Quality Systems Engineer - Remote
Location: San Diego, CA
Duration: 12 Months Total Hours/week: 40 1st Shift
Client: Medical Devices Company Job Category: Professional Level of Experience: Senior Level Employment Type: Contract on W2 (US Citizens, GC Holders, GC EAD, OPT, EAD, or CPT eligible)
Note: This is a hybrid position. Remote work may be considered on a case-by-case basis.
Responsibilities- Define and implement software design and development processes and design control deliverables that adhere to regulatory standards within the medical device industry.
- Lead software process definition and remediation of design documentation to ensure end-to-end traceability and compliance with regulatory requirements (e.g., FDA guidance, IEC 62304, IEEE standards).
- Remediate design control documentation for accuracy, completeness, and clear upstream/downstream traceability from software-centric design control elements.
- Lead continuous improvement efforts, collaborate with multi-disciplinary teams, and provide technical expertise to ensure successful project outcomes.
- Translate business and regulatory requirements into comprehensive software development processes; communicate status and concepts to stakeholders at varying levels of technical ability.
- Facilitate cross-functional collaboration across Systems, Hardware, Test, Quality, and other departments to resolve alignment or feasibility issues.
- Apply best practices from methodologies such as DFSS and Critical Parameter Management to projects; review and remediate software design control documentation.
- Software Process Definition: Develop and implement software processes that comply with industry standards and regulations (e.g., IEC 62304, FDA guidance, IEEE standards) across the full software development lifecycle.
- Software Design Documentation Remediation: Create or modify software design documentation templates within the Quality Management System; ensure end-to-end traceability and remediate gaps and errors as needed.
- Leadership: Transform regulatory requirements into comprehensive software development processes; maintain clear communication with team members and leaders; identify risks and implement mitigations.
- Cross-Functional Collaboration: Enable knowledge sharing across departments to resolve alignment or feasibility issues; communicate project status and design details to stakeholders.
- Continuous Improvement: Identify opportunities to improve software engineering processes for efficiency, quality, and compliance.
- Technical Expertise: Provide guidance on process and documentation; apply DFSS and related practices to projects; review and remediate software design control documentation.
- Bachelors degree in Science or Engineering required; postgraduate degree preferred
- Minimum 5 years of related work experience in software engineering, medical device development, or similar; experience with regulatory standards (IEC 62304, FDA guidance, IEEE) in a regulated industry highly preferred
- Demonstrated ability to lead multi-disciplinary engineering teams and serve as a technical leader
- Positive attitude with critical thinking; willingness to learn and adapt
- Strong organizational skills; ability to work independently and in a team; ability to handle multiple tasks and prioritize
- Strong background in software engineering, testing, and requirements management
- Experience in software product development: needs assessment, system analysis, architectural design, integration and testing, reliability engineering, project management, and FMEA
- Experience creating and maintaining design and development documentation; knowledge of DFSS or statistical test design is preferred
- Experience in Quality engineering and design control management is a plus
- Experience with ALM/PLM tools is a plus
- Excellent communication skills and attention to detail; ability to work in an agile environment is a plus
- Must be legally authorized to work in the United States without sponsorship now or in the future
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