Pharma QA Auditor — On-Site Spokane | Impact & Growth

Jubilant HollisterStier LLC; Spokane (WA); On-site; USD 40,000 - 54,000; Full time

Benefits offered by this job

Medical coverage

Dental coverage

Vision coverage

FSA/HSA

Life Insurance

AD&D Insurance

Disability Insurance

Employee Assistance Program

Job summary

Jubilant HollisterStier LLC in Spokane, WA is hiring a QA Auditor to provide QA inspection and auditing of manufacturing operations ensuring labeling, dating, and packaging meet SOPs and cGMP.

The role involves reviewing product records, keeping lines clean, performing visual vial inspections, and driving corrective actions. Requires a high school diploma, 1 year of related experience, and LMS/MIS familiarity.

Qualifications

• High school diploma or equivalent.
• Minimum 1 year related experience (no degree).
• Electronic documentation management system and/or LMS experience.
• cGMP and pharmaceutical manufacturing knowledge.
• Recognize deficiencies in product quality and report to supervisor.
• Thorough understanding of QA and manufacturing systems related to testing and packaging operation and batch records.
• Working knowledge of Microsoft Office.

Responsibilities

• Process final container samples; inspect per SOP/Protocol/client memo.
• Review and approve product records for completeness and accuracy.
• Ensure labeling/packaging lines are clean and free of materials from previous lots; perform visual inspection of vials and packaging.
• Audit that cGMPs are followed in manufacturing and finished product packaging areas.
• Document deficiencies and coordinate corrective actions with department supervisors.
• Conduct annual retention sample inspections.
• Other tasks as assigned.

Skills

MS Office

QA auditing

cGMP knowledge

Documentation Mgmt Systems

Problem recognition

Education

High school diploma or equivalent

Job description

Jubilant HollisterStier LLC in Spokane, WA is hiring a QA Auditor to provide QA inspection and auditing of manufacturing operations ensuring labeling, dating, and packaging meet SOPs and cGMP.

The role involves reviewing product records, keeping lines clean, performing visual vial inspections, and driving corrective actions. Requires a high school diploma, 1 year of related experience, and LMS/MIS familiarity.