Jobs at Eitan Medical

Leads global clinical operations for a medical device company, overseeing clinical teams, education, training, implementation, quality improvement, patient safety, regulatory compliance, budgets, KPIs, and clinical project management. Partners with executives, sales, marketing, regulatory, quality, and customers to support product adoption and accurate clinical translation. Provides strategic direction, team development, and industry representation across infusion therapy markets.

Leads regulated medical device manufacturing operations, manages production team leaders and staffing, oversees production and final testing processes, and ensures quality, compliance, and procedural adherence. The role drives Lean and continuous improvement initiatives, collaborates with Quality and Engineering, supports employee recruitment and development, and manages manufacturing documentation and operational performance using SAP ERP and Microsoft Office.

Develops healthcare business across Southeast England by growing market share, retaining strategic NHS accounts, pursuing tenders, identifying market opportunities, shaping infusion solutions, engaging senior stakeholders, and increasing revenue. Focus areas include palliative care, acute pain, oncology, and hospital-at-home services. The role requires strong NHS market knowledge, complex stakeholder management, consultative selling, pricing, negotiation, account strategy, and customer relationship development.

Manage end-to-end bookkeeping through trial balance, including VAT and tax reporting, supplier and customer transactions, intercompany reconciliations, multi-currency accounting, month-end close, fixed assets, collections, expense reimbursements, and audit support. The role requires maintaining accurate financial controls in a global environment and reporting to the Company Controller.

Leads mechanical design and development of multidisciplinary medical devices, primarily infusion pumps and accessories, from concept through production. Responsibilities include mechanism development, compact electro-mechanical packaging, engineering documentation, hands-on assembly and testing, and ongoing product support. Requires extensive electro-mechanical product design experience, precision drive mechanism expertise, proficiency with SolidWorks and PDM, and familiarity with medical device regulations.

Manage and optimize Azure cloud-native SaaS platforms, primarily AKS-based Kubernetes environments. Responsibilities include infrastructure automation, IaC, CI/CD and GitOps improvements, monitoring, reliability, security, troubleshooting, release management, and developer productivity tooling. The role supports production and non-production environments and requires collaboration with development, architecture, and operations teams.

Manages supplier quality processes, including supplier approval, SCARs, audits, scorecards, agreements, and performance trending. Serves as CAPA Coordinator and subject matter expert, overseeing CAPA development, risk assessment, execution, verification, and closure. Generates quality metrics for management reviews, maintains quality-system documentation, and ensures compliance with procedures and international standards.