tyForvis Mazars is hiring experienced professionals for a leading pharmaceutical client engaged in Metered Dose Inhaler (MDI) manufacturing. We are looking for validation professionals with robust expertise in pharmaceutical equipment qualification, utility validation, HVAC systems, and GMP-compliant validation practice
s.This role offers an opportunity to work on state-of-the-art pharmaceutical manufacturing facilities while ensuring compliance with global regulatory standard
s.
Key Responsibilit
iesEquipment Qualificat
ionExecute Equipment Qualification activities including IQ, OQ, PQ, and requalificati
on.Prepare, review, and execute Validation Protocols and Repor
ts.Perform qualification of manufacturing and packaging equipment used in MDI producti
on.Support Factory Acceptance Testing (FAT) and Site Acceptance Testing (SA
T).Coordinate with Engineering, Production, QA, and Maintenance teams during qualification activiti
es.Utility Validat
ionQualification and validation of pharmaceutical utilities includi
ng:Compressed
AirNitrogen Syst
emsVacuum Syst
emsPurified Water Syst
emsSteam Syst
emsChilled Wa
terProcess Ga
sesPrepare risk assessments and impact assessments for utiliti