India's DMPLOI - Jobs & Networking AppNeuland Laboratories Limited, one of India’s leading API pharmaceutical manufacturers, has announced a Walk-In Interview Drive for experienced professionals in Production, Quality Control (QC), and Quality Assurance (QA). This recruitment drive is an excellent opportunity for candidates with API pharmaceutical experience who are looking to advance their careers with a reputed pharmaceutical organization.
The company is seeking talented professionals for multiple roles at its Unit-3 facility located in Gaddapotharam, Hyderabad. Candidates with relevant experience in API manufacturing, analytical testing, automation systems, and quality management are encouraged to attend the interview.
Available Positions
Production Department
Roles:
Intermediate & Cleanroom Operations
Production DCS (Automation)
Designation: Chemist / Officer
Experience: 3–6 Years
Qualification: B.Sc., M.Sc., or B.Tech (Chemical)
Quality Control Department
Role:
HPLC, GC, Wet Analysis & LCMS
Designation: Officer
Experience: 4–6 Years
Qualification: B.Sc., M.Sc., or B.Pharmacy
Quality Assurance Department
Role:
AQA
Designation: Officer / Executive
Experience: 5–8 Years
Qualification: B.Sc., M.Sc., or B.Pharmacy
Job Location
Neuland Laboratories Limited – Unit-3, Gaddapotharam, Hyderabad
Important: API Pharma experience is mandatory for all positions.
Walk-In Interview Details
Date: 13th June 2026 (Saturday)
Time: 10:00 AM to 4:00 PM
Venue
Talent Acquisition Centre
Bhagyaradhi Degree College, 1st Floor, Near IDPL X Roads, Hyderabad
Additional Benefits
Competitive salary package
Joining bonus for eligible early joiners
Career growth opportunities in a leading API pharmaceutical company
Exposure to advanced manufacturing and quality systems
Documents Required
Candidates should carry:
Updated Resume/CV
Last two months’ salary slips
Latest increment letter
Educational and experience documents
Technical FAQs
1. What is the purpose of DCS (Distributed Control System) in pharmaceutical production?
DCS is an automation system used to monitor and control manufacturing processes. It helps maintain process consistency, improves operational efficiency, reduces human error, and ensures compliance with GMP requirements.
2. Why is HPLC widely used in Quality Control laboratories?
HPLC (High Performance Liquid Chromatography) is used for the identification, quantification, and purity analysis of pharmaceutical compounds. It provides high accuracy, precision, and reproducibility for API and finished product testing.
3. What is the role of LCMS in pharmaceutical analysis?
LCMS (Liquid Chromatography-Mass Spectrometry) combines chromatographic separation with mass detection. It is used for impurity profiling, trace-level analysis, degradation studies, and structure confirmation of pharmaceutical compounds.
4. What are the key responsibilities of Quality Assurance in API manufacturing?
Quality Assurance ensures compliance with GMP guidelines, reviews manufacturing and laboratory records, manages deviations, conducts audits, handles change controls, and ensures product quality throughout the manufacturing process.
5. What are cleanroom operations and why are they important?
Cleanroom operations involve manufacturing activities performed in controlled environments with regulated particulate and microbial levels. They help prevent contamination, maintain product quality, and ensure regulatory compliance.
Candidates with relevant API pharmaceutical experience are encouraged to attend the Neuland Laboratories Walk-In Interview and explore exciting career opportunities in Production, Quality Control, and Quality Assurance.
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