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Sequel Med Tech is seeking a Staff Validation Engineer to support our growing portfolio of Enterprise systems. The Staff Validation Engineer is responsible for developing, executing, and maintaining validation deliverables to ensure compliance with regulatory requirements. This role focuses on ensuring systems and processes meet operational and regulatory standards. It involves collaboration with cross-functional teams to support validation activities throughout the system lifecycle. You will also serve as the subject matter expert to support our team of full-stack engineers in developing their automated tests and will review and approve delivered features to ensure testing completeness. The ideal candidate for this role will have experience with both manual and automated testing strategies and will know how to communicate effectively with engineers, product leaders, and quality stakeholders.
Job Responsibility:
Oversee day-to-day validation activities of the Enterprise Systems
Develop, execute, and maintain validation deliverables, including validation plans, specifications, protocols, summary reports, and SOPs
Conduct Computer System Validation (CSV) activities in compliance with FDA 21 CFR Part 11, and ISO guidelines
Perform / Support risk assessments, gap analyses, and remediation for validation projects
Collaborate with cross-functional teams to support change management processes and assess the impact on validated systems
Participate in internal and external audits and regulatory inspections, addressing validation-related queries
Support lifecycle management of validated systems, including implementation, maintenance, and decommissioning
Contribute to the development and improvement of validation policies and procedures
Ensure the validation team is well-trained and equipped to support GxP Operations
Design and implement test cases for functional and automated testing, ensuring comprehensive coverage of requirements
Stay current with evolving regulatory expectations (CSA, GxP, SaMD) and technological advancements in validation and testing
Requirements:
BS in Computer Science, Software Engineering, or a related field, or equivalent professional experience
6+ years’ experience in software industry
Medical device or other regulated industry experience required
3+ years’ experience with automated and technical verification
Ability to create and maintain validation deliverables such as validation plans, test plans, test cases, and test protocols
Effectively communicate the status and needs of the validation to engineers, product manager, and Quality partners
Broad experience with a range of test approaches and principles, what types of tests to use, when, and a general understanding of how
Familiarity with validating or hands-on experience with systems like Veeva Vault QualityDocs, Veeva QMS, Arena, ERP, Salesforce, AWS, Azure, GitHub, MuleSoft or similar tools
Familiarity with frontend and backend development principles
Familiarity with CI/CD pipelines and DevSecOps processes
Experience with test case development, automated & functional testing according to requirements and test plans with attention to detail
Experience with test automation tools and frameworks
Ability to design, develop and maintain automated test suites
What we offer:
401k plan with a 6% company match and 100% immediate vesting
Capped out-of-pocket insulin costs and GLP-1 coverage across all plans
Variety of Meritain health insurance plans
Flexible Spending Accounts (FSAs) or Health Savings Account (HSA)
Vision and dental coverage
Voluntary options such as long-term disability, accident, critical illness, hospital indemnity, and pet care discounts
Employer-paid short-term disability and life insurance