GSK
QAValidationSpecialist1(1YearContract)
“QA Validation Specialist 1 (1-Year Contract) at GSK. Skills: Validation, Quality assurance, Regulatory guidance. Provide QA oversight for validation projects. Lead cleaning validation strategy”
Industry & Context.
Problem solvers
What They're Looking For.
Must Have
Bachelor's degree in science, 5 years' experience in QA, Practical knowledge of cGMP, Experience authoring validation documents, Experience assessing impact of changes, Communication skills with stakeholders
Nice to Have
Experience with computerized system validation, Validation strategy experience, Project management experience, Familiarity with continuous process verification
What You'll Do.
Provide QA oversight for validation projects
Lead cleaning validation strategy
Author validation plans
Review validation protocols
Approve validation reports
Assess validation impact for changes
Assess validation impact for deviations
Assess validation impact for investigations
Act as QA approver for deviations
Act as QA approver for CAPAs
Act as QA approver for change controls
Act as QA approver for SOPs
Approve engineering activities
Provide subject-matter expertise on validation
Support preparing validation documentation
Respond to technical queries
Apply regulatory guidance
How You'll Work.
Team & Collaboration
Cross-functional teams; Manufacturing teams
Process & Methodology
Project management
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