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Micro Labs Limited Announces Major Walk-in Drive for Bangalore Positions, Interview in Goa
In a significant recruitment initiative, Micro Labs Limited, a leading name in the pharmaceutical industry renowned for its commitment that “Health is in small details,” has announced a walk-in interview for a wide range of positions destined for its Bangalore location. The drive is scheduled for Sunday, November 9, 2025, at the Goa Woodlands Hotel in Margao.
This event aims to recruit experienced professionals across several critical domains, including Sterile Production, Microbiology, Information Technology (IT), and Project Engineering (Civil). The company is seeking to bolster its team with skilled individuals who can contribute to its high standards of pharmaceutical manufacturing.
Interview Venue & Timing
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.
Open Positions and Eligibility
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.
Documents to Carry
Interested candidates must come prepared with copies of their:
· Updated Resume
· Educational Mark Sheets
· Experience Certificates
· Latest Salary Certificate
· Last Three Months’ Pay Slips
· One Recent Photograph
Alternative Application Method
Candidates who cannot attend the walk-in in person are requested to forward their resumes to Mr. Srinivasa M via email at naveenkumarp@microlabs.in.
For any further queries regarding the recruitment drive, candidates can contact the hiring team at 080-27839033, 34 & 38.
FAQ:
1. What types of sterile formulation products are handled in Micro Labs’ Sterile Production department?
Answer:
The Sterile Production department primarily handles the manufacturing of sterile dosage forms such as eye drops, injections, and BFS (Blow-Fill-Seal) formulations. Equipment used includes ampoule/vial washers, ROTA and Groniger filling machines, BFS lines, and autoclaves—ensuring compliance with aseptic manufacturing and regulatory requirements (like WHO-GMP, MHRA, and USFDA).
2. What kind of experience is required for candidates applying to the Microbiology department?
Answer:
Candidates should have hands-on experience in sterile facility microbiology operations, including Environmental Monitoring (EM), Water Analysis, Microbial Limit Test (MLT), and Sterility Testing. Familiarity with QMS documentation, media preparation, and data integrity in LIMS systems is essential, along with exposure to regulatory audits.
3. What technical skills are expected from candidates in the Information Technology (IT) department?
Answer:
IT professionals should have experience in pharma-plant automation and compliance, particularly with installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) of QC and Production software. Knowledge of 21 CFR Part 11 compliance, server/network configuration, data integrity protocols, and audit trail management is crucial.
4. What are the key technical responsibilities of a Civil Engineer in Project Engineering (Civil)?
Answer:
Civil Engineers are responsible for planning, design, and execution of pharmaceutical facility civil works, ensuring GMP layout compliance, HVAC and utility coordination, and cleanroom construction. Proficiency in AutoCAD, MS Project, BOQ preparation, vendor coordination, and safety norms is also expected. Senior engineers should manage project timelines and cross-department coordination.
5. What GMP and regulatory standards should candidates in production and quality departments be familiar with?
Answer:
Candidates should be knowledgeable about Good Manufacturing Practices (GMP) as per Schedule M, WHO, MHRA, EU-GMP, and USFDA. Understanding QMS elements like change control, deviation management, CAPA, batch manufacturing records (BMR), and aseptic process validation is mandatory for roles in Sterile Production and Microbiology.
