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 solid 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