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. Join Our Team as a system architect at DRS RADA Technologies! Technical Characterization and system Design:
* Spearhead the technical characterization, system design, and architecture of radar-based electronic systems.
* Drive innovation and efficiency in system design processes, ensuring optimal performance and reliability. Leadership in Field and Lab Experiments:
* Lead field and lab experiments to validate and optimize system functionalities.
* Collaborate with cross-functional teams to plan system tests layout, ensuring comprehensive and insightful results. Performance data Analysis:
* Analyse system performance data to derive meaningful insights and recommendations.
* Implement data -driven improvements and optimizations to enhance overall system efficiency.

Rapid Medical is a fast-growing medical device company focused on developing, manufacturing, and selling innovative devices for endovascular interventional procedures. We are seeking a talented QA/RA Engineer to join our quality and regulatory team, playing a dual role that ensures our products meet the highest quality standards while navigating complex global regulatory requirements.
SCOPE & RESPONSIBILITIES Quality Assurance • Manage ECOs: conduct risk assessments, update relevant DMR documents and carry out necessary IQ, OQ, PQ activities if required, finalization of implementation tasks. • Manage DCOs in the PLM system: write and update QA procedures to ensure compliance with quality standards and regulatory requirements. • Manage NCR and CAPA processes: lead, write and supervise the NCR and CAPA processes, ensuring timely and effective resolutions. • Manage QA production activities: provide quality support to production operations, addressing deviations and non-conformities to maintain high product quality. • Ensure timely resolution of quality issues: promptly address all identified or assigned quality issues to prevent delays and maintain efficient operations. • Participate in internal and external audits, such as FDA inspections and notified body audits based on ISO 13485, EU MDR, and MDSAP requirements. • Supplier Quality Management: manage supplier qualification and performance monitoring, including SCAR management, and support supplier audits.
Regulatory Affairs • Prepare, coordinate, track, and follow up on submissions for medical devices across various international markets. • Prepare and manage EU MDR technical documentation submissions. • Oversee CER, PMS, and PMCF activities, including customer complaints, vigilance, and recall. • Participate in regulatory inspections and audits. • Prepare regulatory assessments for design changes. • Develop labeling according to applicable regulatory requirements. • Evaluate and communicate regulatory impact of ECOs and design changes across QA and RA domains.

Lead the Product Management function across multidisciplinary development teams, driving best-in-class product ownership methodologies from concept to launch. Act as the strategic commercial bridge between global field teams and R&D, evaluating business needs for ROI and strictly enforcing R&D intake phase-gates to manage WIP limits. Own and author the Product Requirements Document (PRD) & Marketing Requirements Document (MRD), seamlessly translating complex clinical and business workflows into definitive technical product specifications. Drive usability engineering and human factors testing (IEC 62366-1) specifically tailored for complex medical aesthetics devices Cross-Functional Collaboration with system Engineering, Hardware, Software, V&V, Clinical and Regulatory teams to ensure product vision is executed without scope & feature creep. Play a pivotal role in shaping innovative, broad, and technologically advanced medical products. Ensure alignment between product management and regulatory/clinical/quality requirements. Recruit, mentor, and manage a high-performing team of Product Managers / Product Owners as the department scales Standardize product management frameworks, methodologies (for PRDs/MRDs), and lifecycle processes within the R&D division