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Neuland Laboratories Announces Walk-In Drive for Production & Quality Control Professionals
Neuland Laboratories Limited, a globally recognized pharmaceutical company specializing in API manufacturing, has announced a walk-in recruitment drive for experienced professionals in Production and Quality Control departments. This hiring initiative presents an excellent opportunity for candidates looking to advance their careers in a reputed organization with strong industry presence.
Open Positions
1. Production Department
Roles: Intermediate / Clean Room, Production DCS (Automation), Peptide DCS (Automation)
Designation: Chemist / Officer
Experience: 3–6 Years
Qualification: B.Sc / B.Tech (Chemical) / M.Sc
2. Quality Control Department
Roles: HPLC, GC & Wet Analysis
Designation: Officer
Experience: 5–7 Years
Qualification: B.Sc / M.Sc / B.Pharmacy
Work Location
Neuland Laboratories Limited
Unit-1 (Bonthapally) & Unit-3 (Gaddapotharam), Hyderabad
Note: Candidates must have prior experience in API Pharma, which is mandatory for all roles.
Compensation & Benefits
Neuland offers competitive salaries aligned with industry standards. Additionally, a joining bonus may be provided for candidates who can join early.
Walk-In Interview Details
Dates: 4th & 5th April 2026 (Saturday & Sunday)
Time: 10:00 AM to 4:00 PM
Interview Venue
Quality Inn Ramachandra
#31-41/10/1, Revenue Ward No. 58
Duvvada Railway Station Road, Near Flyover
Duvvada, Visakhapatnam – 530046 (AP)
Documents Required
Candidates are requested to bring:
Updated CV
Last 2 months’ salary slips
Latest increment letter
Contact Information
Email: u3recruitment@neulandlabs.com
Phone: 8712228075
FAQ:
1. What analytical techniques are required for Quality Control roles at Neuland Laboratories?
Candidates should have hands-on experience in analytical instruments such as HPLC (High-Performance Liquid Chromatography), GC (Gas Chromatography), and Wet Analysis techniques. Knowledge of method development, validation, and troubleshooting is highly preferred.
2. What is the role of DCS (Distributed Control System) in Production operations?
DCS is used to automate and monitor production processes in API manufacturing. Candidates should understand process parameters, batch monitoring, alarm handling, and basic troubleshooting within DCS systems to ensure smooth and compliant operations.
3. What are the key GMP requirements in API manufacturing?
Good Manufacturing Practices (GMP) include maintaining proper documentation, adhering to SOPs, ensuring data integrity, cleanliness of equipment, and following safety protocols to meet regulatory standards such as USFDA, WHO, and EU guidelines.
4. What experience is expected in cleanroom and intermediate production areas?
Candidates should be familiar with cleanroom classifications, contamination control, gowning procedures, and handling of intermediates. Experience in reaction monitoring, filtration, drying, and maintaining batch records is essential.
5. What is the importance of method validation in Quality Control?
Method validation ensures that analytical methods are accurate, precise, specific, and reproducible. It is crucial for ensuring the quality and consistency of pharmaceutical products and for compliance with regulatory requirements.
