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NATCO Pharma, a trusted name in the pharmaceutical industry, is conducting a walk-in recruitment drive for its Formulation Division in Hyderabad. Scheduled for Saturday, 18th October 2025, this event offers a valuable opportunity for professionals and fresh graduates to join a leading pharmaceutical manufacturer at their Kothur facility.
Available Positions & Eligibility
NATCO is hiring for two core departments:
1. Operators & Supervisors – OSD Production & Packing
Experience: 0–8 years (Freshers from 2024/25 batches are eligible)
Qualification: I.T.I / Diploma / B. Pharmacy
Key Skills:
· Operation of equipment in Granulation, Compression, Coating, Capsule Filling, and Packing lines
· Supervisory roles in production and packing processes
· Good verbal and written English communication
2. Operators & Supervisors – Production (Injectables)
Experience: 3–8 years
Qualification: I.T.I / Diploma / B.Sc. / B. Pharmacy
Key Skills:
· Hands-on experience with Washing and Depyrogenation Tunnel systems
· Supervision of Manufacturing and Aseptic Filling lines
· Knowledge of Quality Management Systems (QMS) and regulatory compliance
Interview Details
Date: 18th October 2025 (Saturday)
Time: 9:00 AM to 2:00 PM
Venue:
NATCO House, Road No. 2, Banjara Hills,
Hyderabad – 34
(Opposite A.P. Productivity Council of Hyderabad)
· Only candidates with relevant Formulation experience and Regulatory exposure will be considered.
· Male candidates are encouraged to apply due to rotational shifts in production areas.
· Candidates must register using the QR code provided in the original advertisement before attending.
Why Join NATCO Pharma?
NATCO Pharma is known for its high standards in pharmaceutical manufacturing and offers a dynamic work environment with opportunities for growth. This walk-in is a direct pathway to becoming part of a team that values quality, innovation, and professional development.
FAQ:
1. What are the key stages in Oral Solid Dosage (OSD) manufacturing?
Answer:
The OSD manufacturing process includes:
Dispensing: Accurate weighing of raw materials.
Granulation: Wet or dry granulation to improve flow properties.
Drying: Removal of moisture using Fluid Bed Dryer (FBD) or Tray Dryer.
Compression: Tablet formation using rotary compression machines.
Coating: Film or sugar coating for protection and aesthetics.
Packing: Blister or bottle packaging with proper labeling and coding.
2. What parameters are critical during tablet compression?
Answer:
Important parameters include:
Tablet weight variation
Hardness and thickness control
Disintegration time
Compression force
Lubrication level
Speed of the press
Operators should regularly check these during in-process checks (IPCs) to ensure consistent product quality.
3. What is the function of a Depyrogenation Tunnel in Injectable production?
Answer:
The Depyrogenation Tunnel is used to sterilize and remove pyrogens (endotoxins) from glass vials before aseptic filling.
It typically operates at 250°C to 300°C for a defined time.
Ensures sterility assurance level (SAL) before vials enter the aseptic area.
Key parameters include temperature, belt speed, and airflow pattern validation.
4. What are key elements of Good Manufacturing Practice (GMP) in production areas?
Answer:
Cleanroom classification (ISO 5 to 8, depending on the operation).
Proper gowning and personnel hygiene.
Line clearance before starting a new batch.
In-process quality checks and documentation.
Equipment cleaning and validation.
Data integrity and traceability in BMR (Batch Manufacturing Record).
5. What is Quality Management System (QMS) and why is it important in injectables?
Answer:
QMS is a structured system of policies and procedures to ensure consistent product quality.
In injectables, QMS covers:
Deviation management
Change control
CAPA (Corrective and Preventive Actions)
Training records
Environmental monitoring and sterility assurance
It ensures compliance with regulatory standards like USFDA, MHRA, and WHO-GMP.
