QA Validation Specialist — Day-One Benefits, Onsite Spokane

Jubilant Pharma Limited; Spokane (WA); On-site; USD 82,000 - 131,000; 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 seeks a QA Validation Specialist to provide technical expertise through document review and approval, including protocols, acceptance reports, SOPs and specifications. You will support projects as a quality representative across production, engineering, maintenance, IT, and technical services to ensure compliant processes and systems.

You will track validation activities, review transfer protocols, write SOPs, and provide QA SME support for change

Qualifications

• Bachelor of Science or 5 year(s) experience in lieu of degree required.
• 2-5 years related validation experience in FDA regulated industry.
• Pharmaceutical manufacturing, SAP experience, project management desired.
• MS Word, Excel and PowerPoint required.

Responsibilities

• Work with production, engineering, maintenance, IT, and technical services to ensure required documentation is developed to support processes.
• Track and provide technical direction for validation of processes and equipment to ensure compliance with policies and current standards.
• Review product transfer protocols and reports, assess impact to product quality and determine actions.
• Create and write required SOPs pertaining to documentation and QA Validation.
• Review and approve validation protocols, acceptance reports, SOPs and specifications.
• Provide QA SME support for change control and system improvement.

Skills

cGMP knowledge

Education

Bachelor of Science or 5 year(s) experience in lieu of degree

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

Jubilant HollisterStier LLC in Spokane, WA seeks a QA Validation Specialist to provide technical expertise through document review and approval, including protocols, acceptance reports, SOPs and specifications. You will support projects as a quality representative across production, engineering, maintenance, IT, and technical services to ensure compliant processes and systems.

You will track validation activities, review transfer protocols, write SOPs, and provide QA SME support for change