Required QA Engineer
Responsibilities:
Be responsible for the quality of a consumer healthcare platform and connected medical devices used globally.
Design, execute, and maintain test plans and test cases for new and existing features.
Investigate complex issues, perform root cause analysis, and work closely with R&D teams to drive resolution.
Collaborate with Product, R&D, Clinical, and Support teams to ensure high-quality product releases.
Validate end-to-end workflows across cloud, mobile, web, and device components.
Contribute to defining effective testing approaches for a variety of system features and use cases.
Continuously identify opportunities to improve product quality, testing coverage, and QA processes.
Gain exposure to innovative medical technologies and help shape products that impact patients and healthcare providers worldwide.

We are looking for a Software Automation Engineer to join our QA team and to take part in the testing process from planning to execution.
Responsibilities:
Responsible for QA processes, testing and release to production of multiple SaaS products.
Build the test plan for the products.
Identify the risks and appropriate test coverage to validate new features as well as regression and develop test plans and cases.
Lead the test execution and preparation for release.
Execute test cases, manually or in an automated fashion, capture and analyze the results, document issues and prepare test reports.
Work with the R&D and Product to deliver high-quality tested SaaS products.
Write test automation for APIs, UI and stress-testing, as an integrated member of an agile R&D team, building a robust application.
Take responsibility for the quality delivery of product releases.
Participate in defining and optimizing the R&D work processes.

Required QA Specialist
Description
An international Medical Device company that develops and manufactures innovative medical equipment. Specifically, we develop infusion pumps and their related accessory products.
Job Description:
supplier approval/disapproval including supplier maintenance and issuance of the Approved Supplier List.
Leading the SCARS process including SCAR initiation, SCAR follow up, Supplier investigation approval including root cause analysis and SCAR closure.
Leading the supplier audits process (including initial and surveillance audits) for critical suppliers, service centers, laboratories etc. by conducting on site / remote audits. Issuance and execution of the supplier audits plan including supplier audits follow up and supplier non-conformance follow up and response approval.
Support the execution of service agreements, quality agreements with suppliers and service centers.
Leading the supplier score card process, including trending.
Serve as Medicals CAPA Coordinator and Subject Matter Expert
Responsible and accountable for CAPA ownership, timely execution, and effectiveness of CAPAs. This includes creation, collaboration with functional teams on Problem Statement writing/Scope identification/Risk Assessment/Containment/Correction/CAPA plans/Verification of local and global compliance to CAPA procedures to ensure timely effective closure of CAPAs
Generate data and key quality trending information for use in periodic reviews like Quality Metric Reviews and Management Review for CAPA and supplier processes.
Work within, and ensure adherence to Quality System procedures, work instructions and other Quality System requirements.
Write, update, release, and sign quality documentation within the Quality management system
Direct manager: QA Compliance Manager

A fast-growing global medical device company that develops and manufactures innovative drug-delivery and infusion solutions across the continuum of care, from hospital to home. We are looking for an experienced V&V Manager to lead our V&V function and team within the R&D
Job Description:
Lead the V&V function and define the verification and validation strategy for new products and design changes.
Manage, develop, and provide technical leadership to a multidisciplinary team of V&V engineers, including goal setting, workload allocation, mentoring, and performance development.
Ensure complete, risk-based test coverage and traceability from product and system requirements through test evidence and final reports.
Review and approve V&V plans, protocols, reports, deviations, and supporting technical documentation.
Oversee system-level hardware, software, mechanical, and disposable-set testing in the R&D laboratory and at external laboratories and subcontractors.
Lead experimental design, data analysis, structured problem-solving, and root-cause investigations.
Plan resources, equipment, schedules, and priorities, and monitor execution against project milestones and quality objectives.
Partner with Systems, R&D, Quality, Regulatory, Clinical, and Project Management teams, and provide V&V support during audits and regulatory submissions.
Reports to: R&D Director.

We are looking for a talented QA Engineer, to join our team. Its a great opportunity to join an innovative, interesting, and fast-growing startup that will change the world of risk assessments.
As a QA Engineer, you will ensure our product meets the highest standards of quality, reliability and performance.
Responsibilities:
Lead and execute comprehensive testing strategies for our complex software solutions.
Design and establish daily quality control procedures and ensure consistent application across all stages of product development.
You will do manual tests, and automation tests as well.
Executing quality strategy, defining, and measuring metrics.
Collaborate with the development team to troubleshoot and resolve issues.
Define quality metrics and make data-driven decisions to improve product excellence.