Validation process documents and technical reports
Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients
Job Summary
Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients.
In this role, you will evaluate, review, and approve validation master plans, protocols, and reports, ensuring compliance with regulatory requirements and company policies.
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
Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients.
Skills & Requirements
Must-have
validation master plans, protocols, and reports
statistical analysis of testing results
validation process documents and technical reports
Good Manufacturing Practices (cGMP) procedures
regulatory requirements and company policies
equipment qualification and calibration
Nice-to-have
AI tools for problem solving
responsible AI practices
continuous learning and professional development
interpersonal skills and collaboration
adaptability and flexibility
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
4 years of relevant experience
6 years of relevant experience
2-3 years of experience in Quality assurance and / Validation function