Capa Lead jobs at Boston Scientific in Israel

Software Lead

As a Software Lead, you'll be responsible for overseeing the technical direction of software development projects, managing development teams, and ensuring deliverables meet quality standards and business requirements.

Main Duties:

• Lead and mentor a team of software engineers, providing technical guidance
• Review code, conduct design reviews, and implement best practices for development
• Resolve complex technical challenges
• Communicate project status and technical considerations to both technical and non-technical stakeholders
• Responsible to design, develop and implement software applications running under Windows in multidisciplinary systems
• Responsibility for products software engineering process while maintaining the required standards (Medical device)
• Analyzing and enhancing efficiency, stability and scalability of software resources

Requirements:

• BSC in Computer Science or related technical field
• 7+ years industry experience
• Proven experience in leading software projects or small teams
• Expert level developing in MS Visual Studio C# using WPF and .NET framework.
• Deep understanding of the SW development t lifecycle
• Experience with C++/C# interoperability (C++ CLI or controlling P/Invoke)
• Experience with design patterns, and GUI design patterns)MVVM/MVC(
• Strong understanding of multithreading and object-oriented programming
• Ability to document requirements and specifications throughout the software development life cycle
• Strong familiarity with Agile methodologies
• Experience working in multidisciplinary environment

Key Responsibilities:

• Coordinate and present information for CAPA and NCEP meetings.
• Support corrective and preventive action processes as a CAPA Mentor.
• Collaborate with project teams to create timelines, identify root causes, and develop solutions.
• Partner with CAPA owners to complete phases promptly.
• Analyze data to ensure CAPA and NCEP metrics are met.
• Monitor CAPA implementation and identify site improvement opportunities.
• Engage in preventive activities and represent the site in Boston Scientific Communities of Practice.
• Build relationships with other functional areas and departments.
• Gather data with cross-functional experts to support corporate and site objectives.
• Promote a culture of continuous improvement and compliance within the Quality group.
• Develop strong relationships with site and divisional management.
• Champion continuous improvement activities.
• Support Quality System processes like audits, management review, and document control.

Requirements:

• Bachelor's degree, preferably in Engineering.
• At least 5 years of experience as a CAPA/QMS/Operations Quality Engineer (mandatory).
• Experience in the Medical Devices/Pharmaceutical industry (mandatory).
• Proven written and verbal communication skills for a wide variety of internal and external stakeholders.
• Proficient in English, both verbal and written.
• Proficient in the MS Office suite (Word, Excel, PowerPoint).