Quality Systems Associate - Entry-Level QA & Compliance

AbbVie

Illinois

On-site

USD 60,000 - 85,000

Full time

14 days+

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Benefits offered by this job

PTO/Time off
Health insurance
401(k)

Job summary

AbbVie seeks an Associate Specialist Quality Systems to provide quality assurance support across manufacturing processes, ensuring compliance with corporate and governmental regulations. The role covers document control, device QA, labeling, validation, training and CAPA. Collaboration with project teams to review quality docs is essential.

The candidate should have a technical degree and 0-2 years in QA, with strong communication and interpersonal skills to deliver tactical quality outcomes.

Qualifications

  • Bachelor’s Degree in a technical/scientific field; experience preferred.
  • 0-2 years’ experience in quality assurance or related area.
  • Knowledge of pharmaceutical, biologics, medical device quality systems preferred.
  • Strong oral and written communication skills.
  • Excellent interpersonal skills a plus.
  • Delivers tactical results to support the quality system.

Responsibilities

  • Provide QA support for manufacturing processes including drug, biologics, device or combination products.
  • Review quality system changes and specifications for products.
  • Process change requests creation, maintenance and implementation.
  • Support project teams with quality documentation activities.
  • Collect and compile key quality metric data.
  • Participate in training and education programs for QA aspects.

Skills

Communication
Interpersonal skills
Quality mindset
Documentation/records

Education

Bachelor’s Degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering or related technical field
0-2 years QA/quality oversight experience

Job description

AbbVie seeks an Associate Specialist Quality Systems to provide quality assurance support across manufacturing processes, ensuring compliance with corporate and governmental regulations. The role covers document control, device QA, labeling, validation, training and CAPA. Collaboration with project teams to review quality docs is essential.

The candidate should have a technical degree and 0-2 years in QA, with strong communication and interpersonal skills to deliver tactical quality outcomes.

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