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MSN Laboratories Announces Walk-In Interviews for Multiple Departments
MSN Laboratories, a distinguished pharmaceutical company certified as a “Great Place to Work” (July 2025 – July 2026, India), has announced a major walk-in interview drive for multiple positions across various departments. This recruitment initiative underscores the company’s continued expansion and its commitment to attracting and nurturing talented professionals in the pharmaceutical sector.
Interview Details at a Glance
Date of Interview: 01st November 2025
Interview Location: Maithri Laboratories Pvt Ltd, Gaddapotharam
This walk-in drive presents a direct opportunity for qualified candidates to engage with the hiring team and explore rewarding career paths within a certified great workplace.
Open Positions and Eligibility Criteria
The company is seeking experienced candidates for the following key departments:
Department Experience Required Key Eligibility
Production 2-8 years Experience in pharmaceutical manufacturing processes.
Research & Development (R&D) 1-6 years BSc/MSc with relevant API (Active Pharmaceutical Ingredient) experience.
Engineering Services 2-6 years ITI Fitter certification required.
Technical Services Dept. (TSD) 3-7 years B.Tech in Chemical Engineering with relevant experience.
Essential Documents for Candidates
Aspiring applicants are requested to come prepared with the following documents to ensure a smooth interview process:
· Updated Resume
· Passport-size Photographs
· Photo Copies of Educational Certificates
· Latest Increment Letter
· Pay Slips from the last three months
· Bank Statements from the last six months
· Copy of Aadhar Card
FAQ:
1. What are the key parameters monitored during API (Active Pharmaceutical Ingredient) manufacturing?
Answer:
In API manufacturing, critical parameters include temperature, pressure, pH, solvent recovery efficiency, reaction time, and yield percentage. Maintaining these within validated limits ensures process reproducibility and product quality. Additionally, in-process controls (IPCs) like TLC, HPLC purity, and loss on drying (LOD) are closely monitored.
2. How is validation different from qualification in pharmaceutical manufacturing?
Answer:
Qualification refers to verifying that equipment, systems, and utilities are installed and operating correctly (IQ, OQ, PQ).
Validation ensures that a process consistently produces results meeting predetermined quality criteria (process, cleaning, and analytical validation).
Both are essential for regulatory compliance (GMP/GDP standards).
3. What are the common utilities used in Engineering Services for pharmaceutical plants?
Answer:
Key utilities include:
Purified Water (PW) and Water for Injection (WFI) systems
Clean Steam and Compressed Air systems
HVAC systems for controlled environments
Effluent Treatment Plants (ETP/STP)
Chillers, Boilers, and Vacuum Systems
Maintenance and calibration of these utilities are crucial for GMP compliance and smooth operations.
4. What are the common analytical used in R&D for API characterization?
Answer:
In R&D, APIs are analyzed using advanced techniques such as:
HPLC/UPLC – for purity and impurity profiling
GC – for residual solvents
FTIR and NMR – for structural confirmation
DSC and TGA – for thermal stability studies
These analyses support process optimization, stability studies, and regulatory filings.
5. What is the role of Technical Services (TSD) in a pharmaceutical organization like MSN Laboratories?
Answer:
The Technical Services Department (TSD) bridges R&D and Manufacturing, ensuring smooth technology transfer and process optimization. Responsibilities include:
Scale-up of lab processes to plant level
Troubleshooting during commercial production
Conducting process validation and optimization studies
Preparing technical documentation for regulatory audits
