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Senior Design Verification Engineer

Job in North Chicago, Lake County, Illinois, 60086, USA
Listing for: Allergan
Full Time position
Listed on 2026-07-13
Job specializations:
  • Business
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 120000 - 180000 USD Yearly USD 120000.00 180000.00 YEAR
Job Description & How to Apply Below
Position: Senior Design Verification Engineer I

Responsibilities

  • Serve as Subject Matter Expert (SME) on lab capabilities, including GMP and non-GMP equipment, software, and data acquisition systems for Design Verification testing.
  • Responsible for equipment and software qualification, SOPs and work instructions, resolving issues, training operators, and representing combination product development on cross-functionally validated systems.
  • Lead lab verification activities, including design verification protocol development, test method development, test execution, data analysis and documentation, and report writing. Support investigations and issue resolutions. Present results to cross-functional teams.
  • Utilize volumetric accuracy equipment and force testing machine. Familiarity with Zwick, viscometers, climate chambers, etc. is a plus.
  • Support data analysis using statistics, experience with Mini Tab is a plus.
  • Develop, validate, and transfer test methods.
  • Utilize machine shop equipment, Solid Works, and 3D printers to design and verify test method fixtures.
  • Experience with Solid Works, Electronic Lab Notebook (ELN) software and electronic DHF tools such as Polarian are preferred.
  • Work in an independent manner under the guidance of a supervisor or technical lead.
  • Comply with applicable policies and procedures, regulatory and safety requirements.
  • Work on cross-functional teams including Quality, Regulatory Affairs, Clinical Team, and global partners.
Qualifications
  • Bachelor’s Degree or equivalent education and typically 10+ years of experience, Master’s Degree or equivalent education and typically 8+ years of experience, PhD and no industry experience necessary.
  • 3+ years of experience in medical device or combination products.
  • Experience with design control, risk management, and regulatory standards including ISO compliance, FDA and ASTM standards, and regulatory knowledge.
  • Knowledge of Good Manufacturing Practices (GMP), Design Controls, Good Documentation Practices (GDP), and FDA regulations.
  • Possess thorough theoretical and practical understanding of own scientific discipline.
Benefits
  • 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 of this 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 any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employer remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.

Abb Vie 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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Position Requirements
10+ Years work experience
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