Join Now
Neuland Laboratories Limited, a leading global API Contract Development and Manufacturing Organization (CDMO) established in 1984, invites talented professionals to join our team at our Unit-3 facility in Gaddapotharam, Hyderabad.
With a focus on innovation, quality, and sustainability, Neuland supports biotechnology and pharmaceutical companies worldwide in developing complex APIs. Join us to advance your career in a USFDA and EDQM-compliant environment with a strong emphasis on work-life balance and career growth (rated 4.1/5 on AmbitionBox).
Walk-In Interview Details
- Date: Sunday, July 6, 2025
- Time: 9:00 AM to 5:00 PM
- Venue: Quality Inn Ramachandra, #31-41/10/1, Revenue Ward No. 58, Duvvada Railway Station Road, Near Flyover, Duvvada, Visakhapatnam – 530046, Andhra Pradesh
- Job Location: Neuland Laboratories Unit-3, Survey No. 10, Plot No. 3-72, JDA Gaddapotharam, Jinnaram (Mandal), Sangareddy Dist., Hyderabad, Telangana – 502319
- Contact: Email CV to brohini@neulandlabs.com or call +91 8712228075 to confirm attendance.
Required Documents:
- Updated CV (2 copies)
- Last 2 months’ payslips
- Latest increment letter
- Educational certificates (B.Sc / M.Sc / B.Pharm / B.Tech)
- Aadhar card and PAN card
- Passport-size photographs (2)
Job Opportunities
Production
- Role: Intermediate / Clean Room / Production DCS (Auto Machine)
- Designation: Chemist / Officer
- Qualification: B.Sc / M.Sc (Chemistry)
- Experience: 3–6 years in API production
- Vacancies: Multiple (exact number TBD)
Responsibilities:
- Operate and monitor DCS (Distributed Control System) for automated production processes.
- Handle intermediate and clean room operations for API manufacturing.
- Ensure compliance with cGMP, SOPs, and EHS standards.
- Maintain Batch Manufacturing Records (BMR) and support audits.
Quality Assurance (QA)
- Role: Analytical Quality Assurance (AQA) & Quality Management Systems (QMS)
- Designation: Officer / Executive
- Qualification: B.Sc / B.Tech (Chemical) / M.Sc
- Experience: 3–8 years in QA for API manufacturing
- Vacancies: Multiple (exact number TBD)
Responsibilities:
- Perform line clearance, BMR/BPR review, and audit trail checks.
- Manage QMS activities, including CAPA, deviations, and OOS investigations.
- Support regulatory audits (USFDA, EDQM) and ensure cGMP compliance.
- Collaborate with production and QC teams for quality assurance.
Quality Control (QC)
- Role: HPLC, GC, LC-MS, and ICP-MS Analysis
- Designation: Officer / Executive
- Qualification: B.Sc / M.Sc / B.Pharm
- Experience: 4–8 years in QC for API manufacturing
- Vacancies: Multiple (exact number TBD)
Responsibilities:
- Conduct analytical testing using HPLC, GC, LC-MS, and ICP-MS.
- Perform method validation, stability studies, and raw material analysis.
- Maintain GLP-compliant documentation and laboratory records.
- Support regulatory inspections and ensure data integrity.
Plant Engineering
- Role: Mechanical Maintenance & Utility
- Designation: Officer / Executive
- Qualification: B.Tech (Mechanical)
- Experience: 5–8 years in API plant maintenance
- Vacancies: Multiple (exact number TBD)
Responsibilities:
- Perform maintenance of reactors, centrifuges, dryers, and utility systems (boilers, chillers, HVAC).
- Ensure equipment reliability and compliance with safety standards.
- Maintain documentation for preventive maintenance and regulatory audits.
- Troubleshoot mechanical issues to minimize downtime.
Projects Engineering (Peptides)
- Role: Mechanical, Electrical, Documentation, and Instrumentation
- Designation: Executive / Assistant Manager
- Qualification: B.Tech (Mechanical, Electrical, or Instrumentation)
- Experience: 5–9 years in API or peptide projects
- Vacancies: Multiple (exact number TBD)
Responsibilities:
- Manage project engineering for peptide manufacturing, including equipment installation and qualification.
- Oversee mechanical, electrical, and instrumentation activities.
- Prepare and maintain project documentation for regulatory compliance.
- Collaborate with vendors and cross-functional teams to meet project timelines.
Why Join Neuland Laboratories?
- Global Leader: Work with a leading API CDMO supporting biotech and pharmaceutical companies across the product lifecycle, with facilities inspected by USFDA, EDQM, and other global regulators.
- Innovative Environment: Join a team of over 1,700 professionals, with a state-of-the-art R&D center and a focus on complex APIs and peptides.
- Work-Life Balance: Rated 3.8/5 for work-life balance on AmbitionBox, Neuland fosters a supportive and collaborative culture.
- Career Growth: Benefit from opportunities for skill development and career advancement in a company with a 4.1/5 employee rating.
How to Apply
- Walk-In: Attend the interview on July 6, 2025, at the Visakhapatnam venue with all required documents.
- For Those Unable to Attend: Email your CV to brohini@neulandlabs.com, mentioning the specific role and department (e.g., “Production Chemist”) in the subject line. Include total experience, current CTC, expected CTC, and notice period.
Note: Candidates must have experience in API manufacturing and exposure to regulatory audits. Those interviewed at Neuland in the last 6 months are ineligible.
About Neuland Laboratories
Founded in 1984, Neuland Laboratories is a publicly listed company headquartered in Hyderabad, Telangana. As a leading API and CDMO provider, Neuland specializes in complex small molecules and peptides, offering end-to-end solutions from clinical development to commercial manufacturing.
With facilities in Bonthapally, Pashamylaram, and Gaddapotharam, Neuland is committed to quality, sustainability, and innovation. Learn more at www.neulandlabs.com.
Important Disclaimer
Neuland Laboratories does not charge any fees for recruitment or authorize agencies to collect payments. Report suspicious job offers or requests to brohini@neulandlabs.com.
Join Neuland Laboratories and contribute to a healthier world through innovative API manufacturing!