QA Auditor: Pharma Packaging Quality On-Site

Jubilant Pharma Limited

Spokane (WA)

On-site

USD 67,000 - 91,000

Full time

4 days ago
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Benefits offered by this job

Medical coverage
Dental coverage
Vision coverage
FSA/HSA
Life & AD&D
Disability insurance
Employee Assistance Program

Job summary

Jubilant HollisterStier in Spokane, WA seeks a QA Auditor to perform QA inspection and auditing of manufacturing operations to ensure compliance with SOPs and cGMP. The role involves sampling, reviewing records, and ensuring proper labeling and packaging.

Requirements include a high school diploma, at least 1 year of related experience, LMS/EDMS familiarity, and strong cGMP knowledge. On-site, weekend shift, with competitive benefits starting day one.

Qualifications

  • Minimum 1 year related experience (with no degree) required.
  • Proficient with electronic documentation management systems (LMS) and data entry.
  • Knowledge of cGMP and pharmaceutical manufacturing processes.
  • Strong ability to recognize and report product quality deficiencies.
  • Solid understanding of QA and manufacturing systems related to testing and packaging.

Responsibilities

  • Process final container samples and inspect according to SOPs or client memo.
  • Review and approve product records for completeness and accuracy.
  • Ensure labeling/packaging lines are clean and free of prior lot materials.
  • Audit to verify cGMPs are followed in manufacturing and packaging areas.
  • Identify deficiencies and coordinate corrective actions with supervisors.
  • Conduct annual retention sample inspections.
  • Other tasks as assigned.

Skills

1 year related experience
LMS / electronic documentation
cGMP knowledge
Microsoft Office

Education

High school diploma or equivalent

Tools

Electronic documentation management system
LMS

Job description

Jubilant HollisterStier in Spokane, WA seeks a QA Auditor to perform QA inspection and auditing of manufacturing operations to ensure compliance with SOPs and cGMP. The role involves sampling, reviewing records, and ensuring proper labeling and packaging.

Requirements include a high school diploma, at least 1 year of related experience, LMS/EDMS familiarity, and strong cGMP knowledge. On-site, weekend shift, with competitive benefits starting day one.

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