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Alcon

Principal, Software Engineer

Posted Yesterday
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In-Office
Lake Forest, CA, USA
128K-166K Annually
Senior level
In-Office
Lake Forest, CA, USA
128K-166K Annually
Senior level
Develops, maintains, tests, and supports software for on-market ophthalmic medical devices and imaging platforms. The role troubleshoots anomalies, evaluates hardware and software changes, manages configuration and change control, supports cybersecurity and regulatory compliance, and coordinates software releases. It collaborates with development, verification and validation, field service, manufacturing, clinical, and customer-facing teams. The position is onsite in Lake Forest, California, with 10–20% travel.
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At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us?


The Principal Software Engineer, Medical Device Systems is responsible for maintaining, enhancing, and supporting software for Alcon's on-market ophthalmic medical devices and imaging platforms. This role requires a strong background in C++, C#, hardware/software interfaces, and medical device or instrumentation systems, with highly desired experience in MATLAB, camera integration, imaging technologies, firmware interaction, FPGA-based systems, LabVIEW, and RTOS environments. The engineer will investigate software anomalies, assess the impact of hardware and component changes, support cybersecurity and compliance initiatives, and implement robust software solutions that ensure product performance, reliability, and patient safety throughout the product lifecycle.


The role serves as a key liaison between engineering, customer-facing teams, product security, verification and validation, and global software development organizations. It ensures that software changes are properly assessed, documented, tested, and released in accordance with quality system requirements and medical device regulations.


The Principal Software Engineer collaborates closely with onshore and offshore development and V&V teams throughout the software development lifecycle, providing technical inputs for testing, validating software modifications, supporting troubleshooting activities, and maintaining software configuration management. The role enables successful delivery of software updates while ensuring adherence to company policies, regulatory requirements, and product quality standards.


 This is an onsite position located at our main campus in Lake Forest, California.


In this role, a typical day will include:

  • Primary function is to code and/or software updates for on-market medical device systems.
  • Collaborate closely with the software development teams, Technical Support, Field Service, Manufacturing, Clinical and other operation organizations to support necessary software changes initiated by reported anomalies, changes in use cases, material or hardware changes that impact software, cybersecurity, regulatory updates, and other.
  • Troubleshoot, and define solutions to meet expectations, and incorporate changes according to defined processes and procedures, in line with industry standards and regulations.
  • Maintain configuration management and change control according to the associated product Configuration Management Plan and Change Control procedures.
  • Document and execute change-related unit and integration tests. Provide inputs for scope, impact, and effective test methodologies for testing.
  • Assure compliance to software release procedures for post-Market changes to on-market products.
  • Travel required, est. 10-20%

WHAT YOU’LL BRING TO ALCON:


  • Bachelor’s Degree or Equivalent years of directly related experience (or high school +13 yrs. Assoc.+9 yrs.; M.S.+2 yrs.; PhD+0 yrs.)
  • The ability to fluently read, write, understand, and communicate in English
  • 5 Years of Relevant Experience

Preferred Qualifications:  


  • Technical Development Methodology for Medical Devices (21 CFR 820.30, ISO 13485)
  • Systems Engineering or Risk Management for Medical Device (ISO 14971)
  • Medical Device Software – Software Life Cycle Processes (IEC 62304)
  • Regulations and Guidelines associated with software development for medical device
  • Microsoft Office suite (i.e., Word, Excel, Visio)
  • Must have C++, C# development experience.
  • Must have a background with hardware/software interfaces within RTOS and Windows environments.
  • Highly desired skills: MatLAB, LabView, FPGA, Firmware, and experience with camera interactions and interfaces.
  • Familiar with object-oriented software design and large software architecture.
  • 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 and internal customers.
  • Solid understanding of Window operating environments (Win11, Win10, etc.)
  • Experience with one or more software configuration management systems and related tools, such as: AWS DevOps,
  • Jira, Git, ADO, GitHub, TFS
  • Knowledge of networking and cybersecurity concepts are a plus.
  • Experience with Microsoft Visual Studios or other integrated development environment (IDE) tools
  •  Prior experience creating and executing software testing at unit, sub-system, integration, and system levels.
  • Familiar with FDA/ISO regulations for software development and/or EUMDR, prefer including IEC 62304
  • Understanding of Software Development Lifecycle Management (SDLC) – (Agile/Scrum, iterative)
  • Good interpersonal & Communication skills to build positive departmental and inter-departmental relationships in a
  • virtual, remote, and asynchronous environment.
  • Medical device experience is preferred

HOW YOU CAN THRIVE AT ALCON:

  • Manage your own workload and schedule while hitting your set targets.
  • Build positive working relationships to achieve positive goals and business objectives.
  • Balance experiencing new environments and working autonomously in a remote sales environment.
  • Alcon provides robust benefits package including health, life, retirement, flexible time off for exempt associates, and much more!

Alcon Careers  

See your impact at alcon.com/careers  


  

ATTENTION: Current Alcon Employee/Contingent Worker

If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.

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Compensation and Benefits

Alcon’s Total Rewards programs are designed to align incentives with business objectives, support our values, and deliver long‑term value. Our compensation approach includes a combination of fixed and variable pay, with short‑term and long‑term incentive opportunities for eligible roles. Our benefits offerings are designed to support associates and their families across key life events, including programs that promote health and well‑being, provide financial security, and support retirement planning.

The salary range posted represents the anticipated hiring range for this role. Actual compensation may vary based on factors such as experience, skills, location, and internal equity, and may fall outside the posted range.

  

Pay Range

$128,350.00 - $166,100.00

  

Pay Frequency

Annual

  

Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to [email protected] and let us know the nature of your request and your contact information.

Alcon Irvine, California, USA Office

15800 Alton Pkwy, Irvine, CA, United States, 92618

Alcon Lake Forest, California, USA Office

20511 Lake Forest Dr, Lake Forest, CA, United States, 92630

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