India's DMPLOI - Jobs & Networking AppIpca Laboratories Limited (Bio-Manufacturing), Pithampur, Madhya Pradesh, has announced a Walk-In Interview Drive for experienced professionals in DP Manufacturing and Engineering & Maintenance departments. This recruitment drive offers excellent opportunities for skilled technicians with experience in aseptic manufacturing, autoclave operations, and engineering maintenance within pharmaceutical and biotechnology industries.
The walk-in interview is scheduled to be conducted in Indore on 14th June 2026 (Sunday).
Walk-In Interview Details
Particulars Details
Company
Ipca Laboratories Limited (Bio-Manufacturing)
Location
Pithampur, Madhya Pradesh
Interview Date
14th June 2026 (Sunday)
Interview Time
10:00 AM to 4:00 PM
Venue
Hotel Papaya Tree, Rau Circle, Indore
Open Positions
1. DP Manufacturing – Aseptic Technician
Qualification: ITI / Diploma or Equivalent
Experience Required: 2–6 Years
Key Responsibilities:
Operation of aseptic area equipment such as filling machines, capping machines, tray loaders, FIT, BIT, and filtration vessels.
Media Fill (Process Simulation) activities.
Airflow visualization studies and smoke studies.
Aseptic filtration and sterile product handling.
Batch execution and documentation.
Qualification and validation activities.
Equipment and area cleaning documentation.
2. DP Manufacturing – Autoclave Technician
Qualification: ITI / Diploma or Equivalent
Experience Required: 2–6 Years
Key Responsibilities:
Preparation of disinfectant solutions.
Autoclave loading and sterilization activities.
Operation and documentation of de-bagging equipment.
Garment lifecycle management and sterilization processes.
Component washing, drying, inspection, wrapping, and assembly.
Qualification and validation support.
Equipment and area management.
3. Engineering & Maintenance – Technician
Qualification: ITI / Diploma
Experience Required: 1–8 Years
Key Responsibilities:
Preventive and breakdown maintenance of pharmaceutical equipment.
Troubleshooting rotating and static equipment.
Maintenance of filling machines, autoclaves, cold rooms, and bioreactors.
CIP/SIP system operation and maintenance.
Equipment installation, commissioning, and qualification.
Maintenance documentation and logbook management.
Documents Required
Candidates attending the walk-in interview should carry:
Updated Resume
Passport Size Photographs
Aadhaar Card / Passport
Birth Certificate
10th Pass Certificate
Educational Qualification Certificates
Current Company Appointment Letter
Current Company CTC Proof
Last 3 Months Salary Slips
Relieving/Experience Letters from Previous Employers
PAN Card
UAN Details
Why Join Ipca Laboratories?
Ipca Laboratories is one of India’s leading pharmaceutical organizations with a strong presence in manufacturing, research, and global healthcare markets. Working in the company’s bio-manufacturing division provides exposure to advanced aseptic processing technologies, validation practices, and GMP-compliant manufacturing environments.
Professionals joining Ipca can gain valuable experience in sterile manufacturing operations, engineering excellence, and regulatory-compliant pharmaceutical production systems.
Technical FAQs
1. What is Media Fill Validation in aseptic manufacturing?
Media Fill Validation is a process simulation study performed using microbiological growth media instead of the actual product to verify that aseptic filling operations can consistently produce sterile products without contamination.
2. What is the purpose of a Smoke Study in sterile manufacturing?
A Smoke Study (Airflow Visualization Test) is conducted to evaluate airflow patterns within cleanrooms and aseptic areas, ensuring that unidirectional airflow adequately protects critical product exposure zones.
3. What is the difference between CIP and SIP systems?
CIP (Clean-In-Place) cleans equipment using automated cleaning solutions without dismantling equipment, while SIP (Sterilize-In-Place) sterilizes equipment using steam or other sterilizing agents before production.
4. Why is autoclave validation important in pharmaceutical manufacturing?
Autoclave validation ensures that sterilization cycles consistently achieve the required temperature, pressure, and exposure time necessary to eliminate microbial contamination and maintain product quality.
5. What are critical interventions during aseptic filling operations?
Critical interventions include activities such as component replenishment, equipment adjustments, and sterile assembly operations performed during production. These interventions must be validated and executed using strict aseptic techniques to minimize contamination risks.
Final Note
Ipca Laboratories has clearly stated that it does not charge any fee for recruitment and has not authorized any agency or individual to collect money on its behalf. Candidates are advised to attend the interview directly with all required documents and beware of fraudulent recruitment offers.
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