Senior Software V&V Engineer, Imaging Systems

Cleerly$153K — $179K *
US-AnywhereRemote in United States
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 5+ years experience in the medical imaging industry focusing on product development or quality assurance.
  • Bachelor's or Master's degree in Computer Science, Information Technology or a related field.
  • Strong programming skills in Python, particularly in data science, statistical analysis, and machine learning.
  • Experience with software quality engineering under regulatory frameworks including ISO standards and CFR regulations.
  • Proficient with project management tools like JIRA and knowledgeable of the software development life cycle.

Responsibilities

  • Lead the development of the V&V plan in compliance with regulatory and quality requirements.
  • Define and implement test strategies and protocols for various performance measures.
  • Build and analyze complex data sets for testing purposes.
  • Conduct statistical analysis and exploratory data analysis.
  • Create and maintain comprehensive test master plans and schedules for multiple projects.
  • Support software development cycles, participating in SCRUMs and providing feedback on V&V deliverables.
  • Collaborate with cross-functional teams to develop detailed test plans and protocols.

Benefits

  • Eligibility for a 15% target annual bonus.
  • Opportunities for stock options and paid benefits.
  • Remote-first team environment promoting collaboration.
  • Emphasis on core values including humility, excellence, accountability, remarkable impact, and teamwork.
  • Commitment to diversifying the candidate pool and valuing all forms of experience.
Full Job Description
About the Opportunity

We are seeking a software verification and validation (V&V) engineer to ensure the quality of cutting-edge products to meet all defined system and subsystem level requirements and are safe, effective, and compliant for their intended clinical use. This role plays a critical part in supporting regulatory submissions and product releases by planning, executing, and documenting comprehensive V&V activities in accordance with FDA regulations, ISO 13485, IEC standards, and other applicable regulatory and quality system requirements.

Key Responsibilities
  • Develop and lead the Design Verification and Validation (V&V) plan in compliance with regulatory and quality system requirements (21 CFR Part 820, ISO 13485, ISO 14971).
  • Define test strategies, protocols, and acceptance criteria for mechanical, electrical, optical, and system-level performance.
  • Build complex data sets to be used in test
  • Statistical Analysis and Exploratory Data Analysis (e.g., descriptive statistics, regression, visualization)
  • Developed test methods and verification protocols for software product
  • Create and maintain test master plans, schedules, and resource allocation for multiple device programs.
  • Participate in software development sprint cycles by supporting the software development team through attending SCRUMs, design reviews, code reviews and providing feedback on software verification and validation deliverables.
  • Collaborate with cross-functional teams to understand requirements and translate them into comprehensive test plans and protocols
  • Data Governance, Access Controls, and PHI Data Handling


Responsibilities

Required Qualifications & Skills
  • 5+ years equivalent work experience in medical imaging industry(Product Development, Quality)
  • Bachelor's or Master's degree in Computer Science, Information Technology, or related field.
  • Experience with non-product software development
  • Strong programming skills in Python across data science, statistical analysis, big data and ML stack
  • Experience with quality engineering under quality system regulations, including but not limited to 21 CFR Part 820, ISO 14971, IEC 62304, QSR, ISO 13485, MDSAP and/or MDD/MDR
  • Expertise in issue tracking and project management tools like JIRA
  • Strong understanding of the software development life cycle and testing life cycle.
  • Excellent problem-solving, analytical, and critical thinking skills
  • Ability to work collaboratively in a remote-first team environment and to communicate effectively with Product Managers, Engineers, and other stakeholders
Impress us more
  • Prior experience in utilizing AWS Cloud Services or an equivalent enterprise cloud service provider
  • Experience in Class II or Class III medical devices is preferred
  • Experience in Cardiovascular imaging system is a major plus


Job duties, activities, and responsibilities are subject to change by our company.

The base salary range for this role varies by location and is aligned to market benchmarks.
  • Candidates located in higher-cost labor markets, including California, Washington, New York, New Jersey, Connecticut, Massachusetts, and Washington, DC represent the middle to high end of the range, while candidates located in all other U.S. locations represent the low to middle end of the range.
  • Final compensation is determined based on location, experience, skills, and internal equity.

This role is eligible for a 15% target annual bonus, resulting in the following base salary and Total Target Compensation (TTC) ranges:
  • Base Salary: $153,000 - $179000
  • TTC: $176,000 - $206,000

*Total Target Compensation (TTC): Total Cash Compensation (including base pay, variable pay, commission, bonuses, etc.) Additionally, stock options, paid benefits, and employee perks are part of your total rewards.

Working at Cleerly takes HEART. Discover our Core Values:
  • H: Humility- be a servant leader
  • E: Excellence- deliver world-changing results
  • A: Accountability- do what you say; expect the same from others
  • R: Remarkable- inspire & innovate with impact
  • T: Teamwork- together we win

Don't meet 100 percent of the qualifications? Apply anyway and help us diversify our candidate pool and workforce. We value experience, whether gained formally or informally on the job or through other experiences. Job duties, activities and responsibilities are subject to change by our company.

About Cleerly

Clearly is an online retailer of contact lenses, eyeglasses and sunglasses. The company was acquired by EssilorLuxottica Canada, and is headquartered in Vancouver, British Columbia. They are one of the largest online contact lens retailers in North America, and the largest seller of prescription eyeglasses online in the world. Founded in 2000 as Coastal Contacts by Roger Hardy and his sister Michaela Hardy, who bought the keyword "contact lens" from AltaVista, which meant that all searches for "contact lens" were accompanied with Coastal Contacts' banner ads. In the first day, they had 30 orders; within the first month, they had $68,000 in sales. In addition to their lower pricing, the firm provided same day fulfillment of online orders. In 2004, Coastal Contacts raised $6 million in an initial public offering, which they used to expand into the United Kingdom and parts of Europe. In late 2004, they acquired a mail order contact lens business in Europe, LensWay. In 2006, they acquired two more companies: one in the Netherlands and one in Japan. By 2009, the firm increased their revenue to $140 million. They moved into the eyeglasses market in 2008. They source parts for eyeglasses from independent manufactures across the globe, but maintains control over final assembly.
Learn more about Cleerly

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