Description

• Drive SOP/WI updates or creation of new processes based upon upcoming standards or process improvements.
• Collaborate with project/program teams to ensure work products comply with procedures, acceptable qualitative        and quantitative criteria, and global standards, regulations, and guidance.
• Generate documentation at the project level including risk assessment per ISO14971, DFMEA, PFMEA
• Perform and lead CAPA projects and activities.
• Work and review incoming inspection report
• Support and provide guidance on Validations

Bachelor’s Degree required in Pharmaceutical Science.