Nova Biomedical

Senior Software QA Engineer

Nova Biomedical$120K — $130K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 5-7 years of experience in software test engineering within medical devices or scientific instruments
  • Bachelor's degree in computer science, engineering, or equivalent experience
  • Hands-on experience with ISO 13485 compliance and FDA regulations
  • Proficient in Azure DevOps or similar project management tools
  • Knowledge of feature, regression, and integration testing methodologies
  • Understanding of Agile and waterfall development lifecycles
  • Experience with 21 CFR Part 11 requirements and third-party communication protocols

Responsibilities

  • Lead the design and execution of software quality assurance strategies
  • Collaborate with cross-functional teams to meet compliance standards
  • Conduct software validation following regulatory guidelines
  • Review and approve software quality documentation
  • Participate in quality audits and manage risk assessments
  • Monitor software quality metrics for continuous improvement
  • Provide training on software quality and validation processes

Benefits

  • Flexible medical, dental, and vision coverage
  • Competitive 401k company matching
  • Bonus program, generous PTO, and paid holidays
  • Tuition reimbursement for professional development
  • Hybrid and flexible work arrangements
  • Company-provided lunch options in select offices
  • Engagement activities and professional development events
Full Job Description
About the role

The Senior Software QA Engineer will be at the forefront of designing product quality into our next-generation clinical and biopharma Osmometer instruments from the start. Utilizing their experience in modern medical device development, this individual will work closely with our Regulatory Affairs / Quality Assurance and Engineering teams to develop overall test strategy for new products under development. This individual will actively propose and lead process improvements to reduce product development timelines while ensuring the quality and security of our solutions are market leading.

You will be accountable for ensuring proper test case coverage, execution, review, and traceability documentation for assigned projects.

What you'll do
  • Lead the development, review, and execution of software quality assurance processes and procedures for assigned projects
  • Collaborate with cross-functional teams to ensure software development and validation activities meet quality and compliance requirements
  • Perform risk assessments and develop mitigation strategies for software-related issues
  • Conduct software validation activities in accordance with regulatory standards (FDA, ISO 13485)
  • Review and approve software documentation, including validation plans, protocols, and reports
  • Participate in internal and external quality audits
  • Monitor and analyze software quality metrics to identify trends and areas for improvement
  • Provide training and support to team members on software quality and validation processes
  • Implement process and tool improvements to bring verification test case writing and approval concurrent with development for iterative development cycles
  • Actively participate as a member the development team, including reviewing work item acceptance criteria, providing inputs into work item estimation, and reporting of test status
  • Execute manual and automated test cases for verification of requirements and work items within a development iteration

What we are looking for in you
  • Proven track record of commercial software test engineering in a medical device, scientific instrument, or similar environment controlling hardware as part of an overall system
  • Bachelor's degree or higher in a relevant computer science, engineering subject, or equivalent commercial software engineering experience
  • Commercial experience testing and shipping medical devices under ISO 13485
  • Familiarity with current FDA requirements and guidance for cybersecurity
  • Familiarity with feature, regression, and integration testing
  • Experience utilizing Azure DevOps or similar systems for backlog, sprint boards, and test case management
  • Understanding and practice of working in, and testing solutions for, regulatory compliant environments
  • Skills in Setup and configuration of PC, server, cloud hosted, and hardware test environments
  • Understanding and experience with both business-oriented Agile and waterfall software development lifecycles
  • Knowledge with 21 CFR Part 11 requirements
  • Experience testing devices to published 3rd party communication protocols and APIs

Physical Requirements for this role include:
  • Ability to work at a computer for extended periods.
  • Ability to lift and carry up to [25-50] pounds as required
  • Ability to communicate effectively via phone, video, and written communication.
  • Ability to occasionally move about the office to access meetings or resources.

Why work for Nova Biomedical
  • Flexible Medical, Dental, & Vision Coverage
  • Competitive 401k company match
  • Bonus Program, Generous PTO and paid holidays
  • Generous Tuition reimbursement
  • Hybrid and flexible work arrangements
  • Professional development, engagement and events
  • Company marketplace for lunch and snacks in our Norwood, MA, Billerica, MA and Westbrook, ME offices
  • Company subsidized cafeteria in our Waltham, MA office

Work Location: Hybrid work schedule on-site in Norwood, 4 days/week on-site

Targeted Salary Range: $120,000- $130,000/year

Nova Biomedical believes in transparency and integrity throughout all we do, including compensation. The provided salary range for this role represents the expected base salary or hourly rate for this opening. Actual compensation will be commensurate with the candidate's experience and may vary based on individual factors such as location, skills, and education.

About Nova Biomedical

Nova Biomedical is a privately held medical device company based in Waltham, Massachusetts. The company develops, manufactures, and sells blood testing analyzers, and provides diagnostic testing solutions for hospitals, clinics, and laboratories worldwide. Nova Biomedical's products are used in critical care settings, emergency rooms, physician offices, and clinics. The company's products include point-of-care blood gas and electrolyte analyzers, as well as benchtop laboratory analyzers. Nova Biomedical was founded in 1976 by Robert C. Collins, and is still owned by the Collins family.
Learn more about Nova Biomedical
Size
1,200 employees
Industry
Founded
1976

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