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Consulting / General Services

Senior SQA Engineer

Lake Forest, Illinois, United StatesOnsiteContractSenior$48–$48 /hrPosted 2 months ago

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Role summary

Seeking a Senior SQA Engineer for a 12-month contract role in Lake Forest, IL. The position requires 7-12 years of SDLC experience in the Pharmaceutical and Medical Device industries, with a strong focus on Software Quality Assurance and Computer System Validation (7+ years). Responsibilities include leading and executing software validation activities, authoring and reviewing deliverables like validation plans, FMEA, IQ/OQ/PQ, and traceability matrices. The role demands a deep understanding of GxP regulations, validation principles, and risk management. Experience with automated testing tools (JIRA, Confluence, HP ALM, Tosca, etc.) is essential. Familiarity with AWS, Databricks, or GitHub is a plus. This is an onsite role requiring strong communication and collaboration skills.

Job Title: Senior SQA Engineer - 26-01466
Job Location: Lake Forest, IL - 60045 (Onsite)
Locals
DL & LinkedIn must
Contract Duration: 12 Months of Contract role
Pay rate: $48.00/hr on W2
USC, GC
Skill Matrix
Candidate should be local and with in 30-40 miles radius. Max 45 miles
7-12 years of SDLC experience in the Pharmaceutical and Medical Device industries.
7+ years of Software Quality Assurance and Computer System Validation experience.
Hands on experience in validation plans, FMEA, requirements, IQ/OQ/PQ, traceability matrices, system releases.
Experience reviewing and approving validation documentation, CAPAs, change controls, and defect management processes.
Strong knowledge of GxP regulations, validation principles, risk management methodologies.
Experience with automated testing tools and platforms (JIRA, Confluence, HP ALM, Tosca, QTest, M-Files or similar systems).
Experience with AWS, Databricks, GitHub, or CI/CD tools is preferred.
Position Type:
Onsite
Required
7+ years of experience in Software Quality Assurance and Computer System Validation within regulated environments.
Hands-on experience authoring and executing SDLC validation deliverables (e.g., validation plans, FMEA, requirements, IQ/OQ/PQ, traceability matrices, system releases).
Strong knowledge of GxP regulations, validation principles, risk management methodologies, and industry best practices.
Demonstrated experience reviewing and approving validation documentation, CAPAs, change controls, and defect management processes.
Familiarity with both Waterfall and Agile software development methodologies.
Experience with automated testing tools and platforms; proficiency with tools such as JIRA, Confluence, HP ALM, Tosca, QTest, M-Files, or similar systems (experience with AWS, Databricks, GitHub, or CI/CD tools is a plus).
Strong communication and interpersonal skills with the ability to effectively influence stakeholders, provide regulatory guidance, and operate independently in a cross-functional environment.
Responsibilities:
Lead and execute software validation activities across the SDLC, including development, review, and approval of deliverables such as validation plans, FMEA/risk assessments, requirements, IQ/OQ/PQ, traceability matrices, and system releases.
Perform independent SQA review and approval of SDLC documentation to ensure compliance with GxP regulations, internal procedures, and industry standards.
Ensure all IT validation packages are inspection-ready and maintain a continuous state of audit compliance.
Collaborate cross-functionally with IT, development teams, and business SMEs to support validation efforts and ensure alignment with business and regulatory requirements.
Review and provide quality oversight for CAPAs, change controls, and software defects, ensuring appropriate validation impact assessment and resolution.
Contribute to validation strategy development and continuous improvement initiatives for regulated IT systems and processes.
Support implementation and validation of automated testing frameworks and tools to enhance efficiency and quality of software validation activities.

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