Production, QA, QC & Microbiology - Sterile Formulation

Roles & Responsibilities
• Handle batch manufacturing and filling activities in sterile area (Injectables, BFS, Eye drops)
• Operate ampoule/vial washing (Macofar), Rota filling, BFS machines and Autoclave
• Conduct media fill studies and equipment qualification
• Lead qualification studies in sterile manufacturing (QA senior roles)
• Perform QC testing for finished products and stability samples
• Conduct analytical method validation and method transfer
• Handle QMS documentation and compliance activities
• Perform microbiological testing including sterility testing, MLT, environmental monitoring
• Ensure adherence to regulatory and GMP guidelines

Qualification
• B.Pharm / M.Pharm

Experience
• Freshers (QC – male candidates only)
• 0–12 years depending on role
• Production: 2–8 years
• QA: 3–10 years
• QC: 0–6 years
• Microbiology: 6–12 years

Skills
• Sterile manufacturing exposure
• Media fill & validation knowledge
• Equipment qualification handling
• Analytical testing & stability studies
• QMS & regulatory documentation
• Environmental monitoring
• GMP & compliance awareness

About The Company
Micro Labs Limited is a leading Indian pharmaceutical company specializing in sterile formulations including injectables and ophthalmic products. The organization operates in regulated markets and provides strong exposure to quality systems, GMP compliance, and large-scale pharmaceutical manufacturing.