Senior Systems Engineer

  • Full-time
  • Salary Min: 109500
  • Salary Max: 208500
  • Workday Global Grade: 18
  • Compensation: USD 109500 - USD 208500 - yearly

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on XFacebookInstagramYouTubeLinkedIn and Tik Tok.

Job Description

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.

Responsibilities

  • 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)

Qualifications

  • 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.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time ofthis posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future. ​

  • 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. ​

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of anybonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's soleand absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. 

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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