QuidelOrtho logo

Senior Software Verification and Validation Engineer (Lead)

QuidelOrtho

Rochester, NY
Full Time
Senior
95k-110k
10 days ago

Job Description

About the Role

The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most - home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. As a Senior Software Verification and Validation Engineer (Lead), you will be responsible for leading verification and validation activities of complex medical devices under FDA regulations, managing a collaborative engineering team, and ensuring regulatory compliance and product quality in a highly regulated environment. This role is based onsite at 100 Indigo Creek Drive (CNP location).

Key Responsibilities

  • Manage V&V resources with testing and debugging system software, serving as a technical bridge between software Development and V&V.
  • Ensure rigorous adherence to design control documentation and internal procedures for post-launch activities, maintaining regulatory compliance and product quality standards.
  • Develop requirements-based manual test procedures.
  • Compile and analyze test results.
  • Document and manage system software defects.
  • Lead in regular scheduling, planning, resourcing, and team meetings.
  • Participate in regular off-hour meetings with the business partner.
  • Understand project goals and timelines, and provide technical leadership to ensure product launch success.
  • Ensure optimal resource allocation and timely project completion while maintaining quality standards.
  • Provide critical oversight in resolving field issues and maintaining product integrity throughout the lifecycle.
  • Mentor and develop team members to help them grow professionally.
  • Perform other work-related duties as assigned.

Requirements

  • B.S. or M.S. Degree in Computer Science, Chemistry, Biochemistry, Biology, Engineering, or a related discipline.
  • 10+ years of experience, preferably leading in a medical device environment.
  • Strong knowledge of software configuration management tools, defect tracking tools, and peer review.
  • Strong understanding of Instrument V&V Theory & Application.
  • Knowledge of IEC 62304 (Medical Device Software - Lifecycle process), ISO 13485, ISO / EN ISO 14971, and FDA QSR experience or equivalent FDA software development requirements.
  • Strong analytical and problem-solving skills.
  • Strong organizational skills and the ability to manage multiple tasks.
  • Experience in product development and experimental design.
  • Ability to work within cross-functional teams.
  • Strong communication skills, written and verbal.
  • Ability to participate in planning and managing projects.
  • Strong working knowledge of product development tools and processes (e.g., Design Input, Design Output, Verification and Validation, Product Risk Management).
  • Knowledge of related quality systems regulations and processes.
  • Computer skills including e-mail, word processing, statistical, spreadsheet, and graphing software.
  • Knowledge of Application lifecycle management (Agile method preferred).
  • Ability to write test plans, test cases, and test reports.
  • Willingness to travel approximately 10%, including airplane, automobile travel, and overnight hotel stays.

Nice to Have

  • Additional skills or experience that are preferred but not required.

Qualifications

  • Educational background as specified in requirements (B.S. or M.S. in relevant disciplines).

Benefits & Perks

  • Salary range of $95,000 to $110,000, bonus eligible.
  • Comprehensive benefits including medical, dental, vision, life, and disability insurance.
  • 401(k) plan, employee assistance program, Employee Stock Purchase Plan.
  • Paid time off including sick time and holidays.
  • Flexible work hours to meet project deadlines.

Working at QuidelOrtho

Our culture puts our team members first and prioritizes actions that support happiness, inspiration, and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked.

Apply Now

Job Details

Posted AtJul 17, 2025
Job CategoryQA Engineering
Salary95k-110k
Job TypeFull Time
Work ModeOnsite
ExperienceSenior

Job Skills

AI Insights

Key skills identified from this job posting

Sign upto access all insights for this job

About QuidelOrtho

Website

quidelortho.com

Company Size

501-1000 employees

Location

Rochester, NY

Industry

Pharmaceutical and Medicine Manufacturing

Get job alerts

Set up personalized alerts for your job search and get tailored job digests for close matches