Night Quality Assurance Specialist - CGMP & Compliance

Cardinal Health

Colton (CA)

On-site

USD 77,000 - 99,000

Full time

4 days ago
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Benefits offered by this job

Medical coverage
Dental coverage
Vision coverage
401k savings plan
HSA

Job summary

Cardinal Health in Colton, CA is seeking a Senior Specialist - Quality Assurance for night shift. The role involves CGMP documentation review for product release, facilities and equipment, and production controls.

You will report quality issues per CGMP and support a safe, compliant manufacturing environment. Qualifications include a BS in Chemistry or Biology and 1–2 years of QA/reregulated experience; English communication skills are essential.

Qualifications

  • Bachelor’s of Science in Chemistry or Biology degree preferred.
  • Effective written and verbal English communication skills required.
  • 1–2 years experience in QA and/or regulated environment highly preferred – cGMP.
  • Pharmaceutical or medical device experience a plus.
  • ISO experience a plus.
  • Quality Assurance background preferred.
  • Lifting: Frequent lifting between 50–75 lbs.

Responsibilities

  • Applies working knowledge of QA concepts to perform varied tasks.
  • Works on projects of moderate scope and complexity.
  • Identifies possible solutions to technical problems and takes action to resolve.
  • Applies judgment within defined parameters.
  • Receives general guidance; may receive more detailed instruction on new projects.
  • Work reviewed for sound reasoning and accuracy.
  • Engage with operations to drive quality system improvements.

Skills

QA experience
cgmp knowledge
ISO experience
English communication
Quality documentation

Education

Bachelor's of Science in Chemistry or Biology

Job description

Cardinal Health in Colton, CA is seeking a Senior Specialist - Quality Assurance for night shift. The role involves CGMP documentation review for product release, facilities and equipment, and production controls.

You will report quality issues per CGMP and support a safe, compliant manufacturing environment. Qualifications include a BS in Chemistry or Biology and 1–2 years of QA/reregulated experience; English communication skills are essential.

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