Review of SOP, SOI, SCI, PMP, as built drawing & guidelines. Review of process validation & cleaning validation protocols & reports.
Conducting Internal Audits and assisting vendor/customer audits.
Review of IQ, OQ & PQ protocols related to equipment
EDUCATION Required: M.Pharma
EXPERIENCE: At least 10 years of Experience in USFDA / MHRA approved INJECTABLE manufacturing facility.