Alcon
Sr. Software Engineer - LCM SW Lead
Alcon, Lake Forest, California, United States, 92630
At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. Join our team to help people #SeeBrilliantly!We foster an inclusive culture and are looking for diverse, talented people to join Alcon. We are hiring for a Sr. Software Engineer - LCM SW Lead in Lake Forest, CA.Responsibilities:
Manage activities associated with software changes for a variety of medical device systems.Coordinate updates performed by the development team and incorporate updates to software as needed.Manage multiple small-scale projects or a few larger projects simultaneously.Collaborate closely with software development teams (both on-shore and off-shore), Technical Support, Field Service, Manufacturing, Product Security, Clinical, and other organizations to implement necessary software changes.Troubleshoot and define solutions to meet expectations, incorporating changes according to defined processes and procedures in line with industry standards and regulations.Maintain configuration management and change control according to the product Configuration Management Plan and Change Control procedures.Ensure compliance with software release procedures for post-market changes to on-market products.Interact with outside vendors, write/modify/convey requirements, and hold outside vendors accountable for their deliverables.Monitor project activities and report status, including feedback on blockers, potential changes to project scope, and recommended solutions.On-site presence required on a regular basis (occasional remote work possible, per project demands).Experience:
BS in Computer Science or related discipline with 3 years’ experience; or 7 years of relevant experience.Experience leading software development change activities or proven leadership abilities.Understanding of software design control and familiarity with product-level design control.Prefer C++ and C# development experience, and familiarity with object-oriented software design.Ability to work cross-functionally with a variety of stakeholders.Ability to work independently, proactively identify issues, recommend and implement solutions, and deliver quality results on schedule while managing multiple tasks.Understanding of Windows operating environments (Win10, Win7, etc.).Experience with one or more software configuration management systems and related tools, such as Confluence, Jenkins, AWS DevOps, Jira, Git, GitHub, TFS.Knowledge of networking and cybersecurity concepts is a plus.Experience with Microsoft Visual Studio, ADO, or other integrated development environment (IDE) tools.Familiarity with FDA/ISO regulations for software development, including IEC 62304.Solid understanding of Software Development Lifecycle Management (SDLC) – Agile/Scrum, iterative.Excellent interpersonal and communication skills to build positive departmental and inter-departmental relationships in a virtual, remote, and asynchronous environment.Medical device experience is preferred.Key Requirements/Minimum Qualifications:
Associates Degree or equivalent years of directly related experience.The ability to fluently read, write, understand, and communicate in English.2 years of relevant experience.Work hours: M-F, standard.Travel Requirements: 0-5%.Relocation assistance: yes.Sponsorship available: yes.
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Manage activities associated with software changes for a variety of medical device systems.Coordinate updates performed by the development team and incorporate updates to software as needed.Manage multiple small-scale projects or a few larger projects simultaneously.Collaborate closely with software development teams (both on-shore and off-shore), Technical Support, Field Service, Manufacturing, Product Security, Clinical, and other organizations to implement necessary software changes.Troubleshoot and define solutions to meet expectations, incorporating changes according to defined processes and procedures in line with industry standards and regulations.Maintain configuration management and change control according to the product Configuration Management Plan and Change Control procedures.Ensure compliance with software release procedures for post-market changes to on-market products.Interact with outside vendors, write/modify/convey requirements, and hold outside vendors accountable for their deliverables.Monitor project activities and report status, including feedback on blockers, potential changes to project scope, and recommended solutions.On-site presence required on a regular basis (occasional remote work possible, per project demands).Experience:
BS in Computer Science or related discipline with 3 years’ experience; or 7 years of relevant experience.Experience leading software development change activities or proven leadership abilities.Understanding of software design control and familiarity with product-level design control.Prefer C++ and C# development experience, and familiarity with object-oriented software design.Ability to work cross-functionally with a variety of stakeholders.Ability to work independently, proactively identify issues, recommend and implement solutions, and deliver quality results on schedule while managing multiple tasks.Understanding of Windows operating environments (Win10, Win7, etc.).Experience with one or more software configuration management systems and related tools, such as Confluence, Jenkins, AWS DevOps, Jira, Git, GitHub, TFS.Knowledge of networking and cybersecurity concepts is a plus.Experience with Microsoft Visual Studio, ADO, or other integrated development environment (IDE) tools.Familiarity with FDA/ISO regulations for software development, including IEC 62304.Solid understanding of Software Development Lifecycle Management (SDLC) – Agile/Scrum, iterative.Excellent interpersonal and communication skills to build positive departmental and inter-departmental relationships in a virtual, remote, and asynchronous environment.Medical device experience is preferred.Key Requirements/Minimum Qualifications:
Associates Degree or equivalent years of directly related experience.The ability to fluently read, write, understand, and communicate in English.2 years of relevant experience.Work hours: M-F, standard.Travel Requirements: 0-5%.Relocation assistance: yes.Sponsorship available: yes.
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