Exciting pharma jobs in API manufacturing! Neuland Laboratories Limited is conducting a walk-in interview on March 6 & 7, 2026, for Chemist/Officer roles in Production (Intermediate, Cleanroom, Hydrogenation, DCS Automation) and Quality Control (HPLC, GC, Wet) at its Unit-3 facility in Gaddapotharam, Hyderabad.
Mandatory API pharma experience required—join a global CDMO leader offering best-in-industry salary and joining bonus for early joiners in pharmaceutical careers in India.
About the Company
Neuland Laboratories Limited, founded in 1984 and headquartered in Hyderabad, Telangana, is a leading global API Contract Development and Manufacturing Organization (CDMO). As a pure-play API manufacturer, it specializes in complex small molecules, peptides, and custom synthesis services for pharmaceutical and biotechnology companies worldwide.
With over 40 years of expertise, Neuland supports clients from clinical trials to commercial scale, boasting 988+ global filings, 300+ API processes developed, and 204+ patents filed. Its facilities hold approvals from major regulators including USFDA, EDQM, TGA, and others, ensuring top-tier quality, compliance, and innovation.
Neuland operates multiple units, including Unit-3 at Gaddapotharam (acquired in 2017), a multi-product site for advanced intermediates and APIs with strong capabilities in development, analytical labs, and pilot plants.
Job Details
- Company Name: Neuland Laboratories Limited
- Experience: 3–6 years (mandatory API pharma experience)
- Qualification: B.Sc. / M.Sc. / B.Tech. (Chemical) / B.Pharm
- Location: Unit-3, Gaddapotharam, Hyderabad, Telangana
- Work Type: On-site (API Manufacturing Facility)
Job Description
Neuland is hiring experienced professionals for its API-focused Unit-3 in Gaddapotharam, emphasizing specialized production techniques and analytical expertise in a regulated environment. These Chemist/Officer roles support intermediate, cleanroom, hydrogenation, automation, and QC operations for high-quality API manufacturing.
Production – Chemist/Officer (Intermediate, Cleanroom & Hydrogenation, Production DCS Automation)
- Department: Production
- Role: API production operations including intermediates, cleanroom, hydrogenation, and DCS automation
- Experience: 3–6 years
- Education/Qualification: B.Sc. / B.Tech. (Chemical) / M.Sc.
Quality Control – Officer (HPLC, GC & Wet)
- Department: Quality Control
- Role: Analytical testing using HPLC, GC, and wet chemistry methods
- Experience: 4–6 years
- Education/Qualification: B.Sc. / M.Sc. / B.Pharm
Skills / Qualifications
- Mandatory experience in API pharmaceutical manufacturing
- Hands-on expertise in hydrogenation, cleanroom operations, and intermediate synthesis
- Proficiency with Production DCS (Distributed Control System) for automation
- Strong knowledge of HPLC, GC, and wet analysis techniques
- Familiarity with GMP, quality standards, and analytical documentation
- Good communication and problem-solving skills
- Ability to work in a regulated, multi-product API environment
Key Responsibilities
- Operate and manage hydrogenation, cleanroom, and intermediate production processes
- Handle DCS automation for production control and monitoring
- Perform HPLC, GC, and wet lab analysis for raw materials, in-process, and finished APIs
- Ensure compliance with GMP, safety, and quality protocols
- Maintain accurate records, calibration, and documentation
- Support troubleshooting and process optimization in API manufacturing
- Contribute to audit readiness and regulatory compliance
Benefits / Perks
- Best-in-industry salary packages
- Joining bonus for early joiners
- Career growth in a global API CDMO leader
- Exposure to advanced API technologies and international regulations
- Opportunities for professional development in a quality-focused environment
How to Apply
Attend the walk-in interview with:
- Updated CV
- Last 2 months’ pay slips
- Increment letter
- Relevant educational and experience documents
If unable to attend, email your resume to [email protected]. For more pharma jobs in Hyderabad, API roles, and CDMO opportunities, visit trusted platforms like Pharma Recruiter.
Walk-in Interview Details
- Date: March 6 & 7, 2026 (Friday & Saturday)
- Time: 10:00 A.M. to 3:00 P.M.
- Venue: Hotel City Inn, City Center, Sahakar Chowk, Above Baramati Bank, Daund, Maharashtra – 413801
Why You Should Join Neuland Laboratories
Neuland offers a collaborative, innovation-driven culture with a strong emphasis on quality, transparency, and agility. As a preferred CDMO partner for global pharma, it provides long-term stability, exposure to complex API development, and the chance to contribute to life-changing medicines.
With a proven track record of regulatory excellence and growth, Neuland is an ideal choice for API professionals seeking rewarding careers in a respected, patient-focused organization.
FAQs
Who is eligible for the Neuland Laboratories walk-in interview?
Candidates with 3–6 years of mandatory API pharma experience; qualifications in B.Sc./M.Sc./B.Tech (Chemical)/B.Pharm.
What documents are required for the walk-in?
Updated CV, last 2 months’ pay slips, increment letter, and educational/experience proofs.
Is email application accepted?
Yes—send resumes to [email protected] if you can’t attend the interview.
What perks does Neuland offer?
Competitive salary, joining bonus for early joiners, and excellent growth in a global CDMO with USFDA-approved facilities.
