Plan and execute verification testing for injection devices and related components
Develop protocols, test methods, acceptance criteria, and summary reports
Analyze test data and evaluate whether design outputs meet requirements
Support device characterization, failure analysis, and troubleshooting activities
Support design reviews, risk assessments, and requirements traceability
Identify gaps in verification strategy and recommend technical solutions
Contribute to technical documentation, change control, and design history file content
Support test method development, equipment setup, and laboratory readiness
Ensure verification activities are performed in compliance with safety, quality, and regulatory requirements (e.g. 21 CFR 820 / Design Controls)
Bachelor's Degree in Mechanical or Biomedical Engineering or other related scientific discipline and typically 12 years of experience, Master's Degree or equivalent education and typically 8-10 years of experience.
Experience in the medical device, combination product, or other related scientific fields with specific focus on lab-based activities.
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
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Dental insuranceVision insurance401(k)Paid time offPerformance bonus
Additional Information
AbbVie is seeking a Senior Verification Engineer to join the PDS&T Injection Device group. In this role, you will lead and support verification activities for injection devices and related combination products, helping ensure that design outputs meet user needs, performance requirements, and regulatory expectations.
You will work closely with cross-functional partners to plan, execute, analyze, and document verification testing across the product development lifecycle. The ideal candidate brings strong technical rigor, attention to detail, and experience supporting regulated device development.
Abbvie · Tempe, AZ