Medical Device Quality Assurance Intern

4 weeks ago


Pleasanton, California, United States AbbVie Full time
Job Opportunity

AbbVie is seeking a highly motivated and detail-oriented Medical Device Quality Assurance Intern to join our team. As a member of our Pharmacovigilance, Patient Safety, Epidemiology, and Quality (PSEQ) organization, you will have the opportunity to work collaboratively with colleagues across the product lifecycle to identify, evaluate, understand, and communicate the safety profile and ensure quality standards of AbbVie products.

The Medical Device Combo Product Research and Development Quality Assurance (MDCP RDQA) organization is responsible for ensuring products are designed to be safe and effective, while also ensuring development efforts comply with applicable standards and regulations. As an intern, you will support a team of R&D QA development partners around the globe, collaborating with Quality Engineers and Managers at the site to:

  • Facilitate the successful execution of the Design Control Process for complex electromechanical medical devices containing hardware, software, electrical and mechanical components.
  • Create Quality Engineering deliverables required within the product development process.
  • Support Design Verification and Validation activities, including review of verification & validation protocols and reports.
  • Assist in the analysis of product requirements and specifications. Participate in product design reviews and team meetings.
  • Provide subject expertise and input in the following areas: Biocompatibility strategy, including requirements, protocol, and report; Shelf-Life Studies strategy, including accelerated and real-time; Cleaning Validation.
  • Ensure that technical information is accurate and in compliance with quality and regulatory requirements.
  • Review Design Changes post design transfer.
  • Work on process improvements globally or at the site level.
  • Prepare information for communication and knowledge sharing using various methods (e.g., presentations, written messages, training, etc.).
  • Learn about R&D QA quality systems in a regulated environment.

Qualifications:

  • Currently enrolled in university, pursuing a Bachelor's degree in Bioengineering, Biomedical Engineering, Mechanical Engineering, or other related scientific/engineering degree.
  • Must be enrolled in university for at least one semester following the internship.
  • Expected graduation date between December 2025 – June 2026.

Preferred Qualifications:

  • Medical device or project management experience.
  • Interest in compliance.

Benefits and Amenities:

  • Competitive pay.
  • Relocation support for eligible students.
  • Select wellness benefits and paid holiday / sick time.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.



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