Join Neuland Laboratories’ walk-in interview on July 6, 2025, in Visakhapatnam for Production, QA, QC, and Engineering roles. USFDA-approved API manufacturing jobs in Hyderabad. Apply today!
Neuland Laboratories Walk-In Interview for Production, QA, QC, and Engineering Roles – July 6, 2025
Neuland Laboratories Limited, a global leader in API Contract Development and Manufacturing Organization (CDMO) services, is inviting experienced professionals to attend a walk-in interview for various technical and quality-focused roles. With a heritage dating back to 1984, Neuland is known for its excellence in complex API development and regulatory-compliant manufacturing.
🚩 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 District, Hyderabad, Telangana – 502319
📧 Contact: Send your resume to brohini@neulandlabs.com or call +91 8712228075 to confirm your attendance.
📄 Required Documents
- Two copies of your updated CV
- Last 2 months’ salary slips
- Latest increment letter
- Educational certificates (B.Sc / M.Sc / B.Pharm / B.Tech)
- Aadhar and PAN cards
- Two passport-size photographs
💼 Job Opportunities at Neuland Laboratories
1. Production
- Designation: Chemist / Officer
- Role: Intermediate / Clean Room / Production DCS (Auto Machine)
- Qualification: B.Sc / M.Sc in Chemistry
- Experience: 3–6 years in API production
Key Responsibilities:
- Operate and monitor DCS systems for automated processes
- Conduct cleanroom and intermediate operations for APIs
- Maintain BMRs, follow cGMP and EHS protocols
- Assist in regulatory audit readiness
2. Quality Assurance (QA)
- Designation: Officer / Executive
- Role: Analytical Quality Assurance (AQA) and QMS
- Qualification: B.Sc / M.Sc / B.Tech (Chemical)
- Experience: 3–8 years in API QA
Key Responsibilities:
- Review BMR/BPR, manage deviations and audit trails
- Handle CAPA, OOS investigations, and QMS activities
- Support USFDA/EDQM audits
- Collaborate with QA/QC teams to ensure compliance
3. Quality Control (QC)
- Designation: Officer / Executive
- Role: HPLC, GC, LC-MS, and ICP-MS Analyst
- Qualification: B.Sc / M.Sc / B.Pharm
- Experience: 4–8 years
Key Responsibilities:
- Analytical testing of raw materials and APIs
- Method validation and stability studies
- Use of HPLC, GC, LC-MS, and ICP-MS
- Maintain GLP-compliant lab practices
4. Plant Engineering
- Designation: Officer / Executive
- Role: Mechanical Maintenance & Utility
- Qualification: B.Tech (Mechanical)
- Experience: 5–8 years
Key Responsibilities:
- Maintain critical plant equipment including reactors and centrifuges
- Ensure compliance with preventive maintenance schedules
- Maintain GMP and safety documentation
5. Projects Engineering (Peptides)
- Designation: Executive / Assistant Manager
- Role: Mechanical, Electrical, Documentation, Instrumentation
- Qualification: B.Tech (Mechanical, Electrical, Instrumentation)
- Experience: 5–9 years in peptides or API projects
Key Responsibilities:
- Execute engineering projects for peptide manufacturing
- Oversee installation, validation, and documentation
- Work with multidisciplinary teams and external vendors
🌟 Why Join Neuland Laboratories?
- Regulatory Excellence: Work in USFDA and EDQM-approved facilities
- Cutting-Edge Innovation: Specializing in complex APIs and peptides
- Career Growth: Over 1,700 professionals with strong internal mobility and mentorship
- Work-Life Balance: Rated 3.8/5 by employees for a healthy work culture (AmbitionBox)
- Global Impact: Partnering with major biotech and pharma companies worldwide
📌 How to Apply
Option 1: Walk-In Interview
- Attend on July 6, 2025, with all the required documents at the Visakhapatnam venue.
Option 2: Email Application
- Send your CV to brohini@neulandlabs.com
- Use subject line: “Application for [Role Name] – [Department]” (e.g., “Production Chemist – API Unit”)
- Mention total experience, current & expected CTC, and notice period.
Note: Candidates with API manufacturing experience and regulatory audit exposure preferred. Applicants interviewed within the last 6 months are not eligible.
🏢 About Neuland Laboratories
Founded in 1984 and headquartered in Hyderabad, Neuland Laboratories is a publicly listed company offering CDMO and API services. The company operates multiple GMP-compliant manufacturing facilities, including those in Bonthapally, Pashamylaram, and Gaddapotharam. Neuland’s focus areas include peptides, oncology APIs, and custom synthesis for global markets.
Learn more at 🌐 www.neulandlabs.com
⚠️ Important Disclaimer
Neuland Laboratories does not charge any fees at any stage of recruitment. If someone demands payment or job guarantees, please report to brohini@neulandlabs.com immediately.
🚀 Build Your Future with Neuland Laboratories Advance your career with a trusted API leader and make a difference in global healthcare innovation. Don’t miss this walk-in opportunity!
