Micro Labs Limited -Walk-in Drive for Multiple Departments on 9 Nov 2025@Goa
Date: 09th November 2025 (Sunday)
Time: 9:00 AM to 5:00 PM
Venue: Goa Woodlands Hotel, Rua Miguel de Loyola Furtado, Opposite City Bus Stand, Margao, Goa – 403601.
The walk-in is being conducted for the following roles, with a specific note that only male candidates are eligible to apply.
1. Sterile Production
This department has openings for leadership,executive, and technical roles focused on the manufacturing of sterile formulations like eye drops and injections.
Assistant Manager / Deputy Manager / Manager
Qualification: B.Pharm / M.Pharm / M.Sc
Experience: 8-12 years in handling regulatory audits, QMS documentation, manpower, and production planning for sterile formulations.
Officer to Senior Executive
Qualification: B.Pharm / M.Pharm / M.Sc
Experience: 2-8 years in batch manufacturing and filling activities (3 Piece, BFS, injectables) within a sterile area.
Technical Staff
Qualification: ITI / Diploma in Pharmacy / Diploma in Engineering
Experience: 2-5 years in operating machinery like ampoule/vial washers, filling machines (ROTA, Groniger, BFS), and autoclaves
2. Microbiology
Assistant Manager / Manager
Qualification: B.Sc / M.Sc in Microbiology or Biotechnology
Experience: 9-14 years in a sterile facility, with responsibilities in QMS, microbial limit testing (MLT), stability, and environmental monitoring.
3. Information Technology (IT)
Assistant Manager / Deputy Manager / Manager
Qualification: Diploma, B.Sc/M.Sc, BE, BCA, or MCA
Experience: 8-12 years in a pharmaceutical plant, with proficiency in installing and qualifying QC & Production software and handling IT audit compliance.
4. Project (Civil Engineering)
Civil Engineer
Qualification: Diploma/B.E./B.Tech in Civil Engineering
Experience: 4-5 years in executing civil works for pharma facilities, with knowledge of AutoCAD and MS Project.
Senior Civil Engineer
Qualification: Diploma/B.E./B.Tech in Civil Engineering
Experience: 10+ years in leading civil design, execution, and coordination for pharma projects, ensuring GMP and safety compliance.