Manufacturing Senior Associate_104865
Core
Managing the lifecycle of controlled GMP documents for manufacturing operations, ensuring accuracy and compliance across SOPs, protocols, and deviation records.
Role type
Senior Document Controller (Manufacturing)
Builds
Controlled document systems and compliance records for manufacturing processes
Domain
Pharmaceutical manufacturing / Biologics / GMP
Required skills
GMP documentation, Document lifecycle management, Deviation tracking, SOP authoring, Stakeholder coordination, Audit readiness, Workflow improvement, Revision scheduling, Compliance monitoring, Right-first-time approval
Preferred skills
Biologics manufacturing experience, Pharmaceutical industry experience
Technologies
GMP systems, Document control software
Responsibilities
Author, revise, and maintain controlled GMP documents; Manage document reviews, approvals, and lifecycle status; Coordinate with cross-functional teams to ensure process accuracy; Support deviation documentation and corrective actions; Monitor documentation metrics and audit readiness; Improve documentation workflows and compliance performance.
