Evaluate, review, and approve validation master plans, protocols, and reports, ensuring compliance with regulatory requirements and company policies
Job Summary
Evaluate, review, and approve validation master plans, protocols, and reports, ensuring compliance with regulatory requirements and company policies.
Contribute to project tasks and milestones, organizing work to meet deadlines and applying basic team effectiveness skills within the immediate Work Team.
Work effectively as a member of the Quality Operations (QO) cGMP training team, collaborating with Business Area Training Leads, Coordinators, and SMEs to support cGMP and site training initiatives.
Matching Summary
Evaluate, review, and approve validation master plans, protocols, and reports, ensuring compliance with regulatory requirements and company policies.
Skills & Requirements
Must-have
validation master plans
validation process documents
cGMP procedures
Microsoft Office, particularly Excel
validation principles and practices
Nice-to-have
AI tools, including generative technologies
pharmaceutical manufacturing
regulatory queries and responses
dynamic work environment
continuous learning
Key Requirements
bachelor's degree with any years of experience
Associate's degree with 4 years of relevant experience
high school diploma with 6 years of relevant experience
2-3 years of experience in Quality assurance and / Validation function