Join Neuland Laboratories Limited, a leading global API Contract Development and Manufacturing Organization (CDMO) founded in 1984, headquartered in Hyderabad, Telangana. With a turnover of ₹1,600 Cr, three USFDA-approved facilities, and operations in 85+ countries, Neuland excels in manufacturing complex APIs and intermediates, supported by a 40,000 sq. ft. R&D center and 1,700+ employees.

Rated 4.0/5 on AmbitionBox for company culture (3.9/5), Neuland is hosting a walk-in interview on May 17, 2025, at Hyderabad for Production and Quality Control (QC) roles at its Unit-2 facility in Pashamylaram, targeting professionals with 3-8 years of experience in API manufacturing.

Event Details: Walk-In Interview

This walk-in drive seeks candidates for Production (Chemist, Officer) and Quality Control (Chemist) roles at Neuland’s Unit-2, a USFDA-compliant facility specializing in API production. Candidates with regulatory exposure are preferred.

Date and Time

Date: Saturday, May 17, 2025
Time: 10:00 AM – 4:00 PM IST

Interview Venue

Pharma Jobs, Talent Acquisition Centre
Bhagyaradhi Degree College, 1st Floor, Near IDPL X Roads, Hyderabad, Telangana

Work Location

Neuland Laboratories Limited
Unit-2, Plot No. 92-94, 257-259, IDA Pashamylaram, Patancheru Mandal, Sangareddy District, Telangana – 502307

Job Opportunities at Neuland Laboratories

We’re hiring for Production and Quality Control roles to support API manufacturing at Unit-2, adhering to cGMP standards. All positions require experience in API or bulk drug environments.

1. Production – Chemist / Officer

Qualification: B.Sc. (Chemistry)
Experience: 3-8 years in API production
Key Responsibilities:
- Conduct shift operations for API synthesis, hydrogenation, or intermediates
- Operate production equipment using DCS (Distributed Control Systems)
- Record process parameters in Batch Manufacturing Sheets (BMS) and Batch Production Records (BPR)
- Ensure compliance with cGMP, Good Documentation Practices (GDP), and safety norms
- Report deviations and coordinate with maintenance for equipment uptime
Key Skills:
- Expertise in shift operations and DCS-based equipment
- Knowledge of cGMP, GDP, and API manufacturing
- Proficiency in BMS/BPR documentation
- Strong troubleshooting and safety awareness
Openings: Multiple (likely 4-6 based on production needs)
Salary: ₹3.5–7.0 Lakhs/year (estimated based on industry standards)

2. Quality Control – Chemist

Qualification: B.Sc. or M.Sc. (Chemistry)
Experience: 3-5 years in QC for API manufacturing
Key Responsibilities:
- Perform testing of raw materials, in-process, and finished APIs using HPLC, GC, and wet analysis
- Conduct method validations and stability studies per ICH Q2(R1)
- Document results in LIMS and ensure GLP/GDP compliance
- Investigate OOS/OOT and support USFDA audits
- Calibrate instruments like HPLC, GC, and pH meters
Key Skills:
- Proficiency in HPLC, GC, and wet chemistry techniques
- Knowledge of GLP, GDP, and cGMP standards
- Experience with LIMS and method validation
- Strong analytical and audit-facing skills
Openings: Multiple (likely 3-5 based on QC lab needs)
Salary: ₹3.5–6.0 Lakhs/year (estimated based on industry standards)

Why Join Neuland Laboratories?

Neuland, with a 4.0/5 AmbitionBox rating, is praised for work-life balance (3.8/5) and supportive culture but faces criticism for moderate career growth (3.3/5). Our Unit-2 in Pashamylaram, one of three FDA-inspected facilities, produces 75+ APIs across 10 therapeutic areas, with 846+ DMFs filed globally.

Employees value regulatory exposure (3.9/5) and collaboration, though QC roles may involve high pressure. With a focus on complex chemistry and a no-compete policy with customers, Neuland offers a rewarding platform for API professionals.

Key Benefits

Work in a USFDA-approved API facility
Gain expertise in DCS, HPLC, and cGMP processes
Contribute to APIs for 85+ countries
Join a collaborative, innovation-driven team
Access Hyderabad’s pharma hub opportunities

How to Apply

Attend the walk-in interview on May 17, 2025, from 10:00 AM to 4:00 PM at Bhagyaradhi Degree College, Hyderabad. Bring:

Updated resume
Educational certificates (B.Sc., M.Sc.)
Experience letters and last 3 months’ payslips
Aadhar and PAN cards
Passport-size photographs (2)
Preparation:
- Production: Review DCS operations, cGMP, and BMS/BPR documentation
- QC: Study HPLC, GC, method validation, and GLP
- Be ready to discuss USFDA audit experience and deviation handling

Neuland Laboratories Limited Walk-In Interview for Production and Quality Control Roles on 17th May

Note: Candidates unable to attend can email CVs to kmdhinakar@neulandlabs.com or WhatsApp +91 8179538447 / +91 7995556802 by May 15, 2025, with subject “Position Name – Hyderabad”. Neuland does not charge recruitment fees; verify communications via @neulandlabs.com emails or listed contacts.

About Neuland Laboratories

Neuland operates three manufacturing units in Hyderabad (Unit-1: Bonthapally, Unit-2: Pashamylaram, Unit-3: Gaddapotharam), with 300+ R&D scientists and certifications from WHO, EMA, and PMDA. Listed on BSE/NSE, we focus on complex APIs and peptides, with zero 483 observations in recent USFDA audits. Our mission is to deliver end-to-end solutions through agility, transparency, and quality.

Our Mission

Advance drug development through complex chemistry
Maintain uncompromising quality and regulatory compliance
Foster a collaborative, employee-centric workplace

Attend the walk-in interview on May 17, 2025, in Hyderabad or email kmdhinakar@neulandlabs.com. Join Neuland’s Unit-2 and drive API innovation!