GSK
Biopharma
QualityValidationandCSVManager
“Quality Validation and CSV Manager at GSK. Skills: Quality Validation, CSV Management, Team Management. Manage validation activities planning. Execute validation activities”
What You'll Achieve.
Deliver safe, effective and compliant products; Accelerate improvements across cross-functional teams
Industry & Context.
Iterative problem solving
What They're Looking For.
Must Have
Degree in relevant Scientific, Technical or Engineering discipline (or equivalent experience), Relevant knowledge/experience within Validation and CSV, Leadership experience, Knowledge of current Good Manufacturing Practice (cGMP) requirements, Knowledge and application of Quality Management Systems (QMS), Knowledge of internal and external audit processes (eg; inspection readiness)
Nice to Have
experience gained working in a manufacturing facility within a highly-regulated industry
What You'll Do.
Manage validation activities planning
Execute validation activities
Maintain validation activities
Ensure compliance with regulatory expectations
Provide technical expertise
Collaborate with cross-functional teams
Develop validation protocols
Review validation protocols
Approve validation protocols
Manage validation lifecycle for computer systems
Represent validation activities for audits
Support adoption of new technologies
How You'll Work.
Team & Collaboration
Collaborate with cross-functional teams (including Engineering, Manufacturing, IT, and Quality teams)
Communication Scope
Effective written communication; Effective verbal communication; Excellent interpersonal skills
Process & Methodology
Align validation activities with project timelines, Align validation activities with business objectives
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