Neuland Laboratories Limited is a globally recognized pharmaceutical company specializing in Active Pharmaceutical Ingredients (APIs) manufacturing and development. With regulatory approvals from USFDA, EDQM, and other global agencies, Neuland is known for its expertise in complex chemistry, contract manufacturing, and high-quality API production, offering strong career opportunities in production, quality, and safety functions.

Founded in 1984, Neuland Labs is a globally recognised Contract Development and Manufacturing Organization (CDMO), offering comprehensive customised NCE development services. Our team comprises highly skilled scientists, engineers, and technicians who utilise their expertise and advanced technologies to address the complex and evolving requirements of our clients.

We collaborate with pharmaceutical and biotechnology companies to support all aspects of their chemistry needs, ranging from early development stages to commercial manufacturing, including process development, optimisation, analytical testing, and regulatory compliance. Neuland Labs possesses the capabilities and flexibility to manage both single-step processes and complete synthesis, handling projects from lab to commercial supply.

We provide quantities suitable for clinical trials as well as full commercial-scale production of new chemical entities (NCEs), key starting materials (KSMs), active pharmaceutical ingredients (APIs), and their intermediates, ensuring efficient tech transfer timelines.

DATE AND TIME:

• Date: 21 February 2026 (Saturday)
• Time: 10:00 AM – 3:00 PM

 Venue & Work Location

Neuland Laboratories Limited
Unit-1, Bonthapally,
Hyderabad, Telangana

 Resume Email: adivvani@neulandlabs.com

JOB DETAILS:

Open Positions

 Production – Intermediates / Clean Rooms

Roles & Experience

• Chemist – 3 to 4 Years
• Officer – 5 to 7 Years

Qualification

• B.Sc / M.Sc – Chemistry

Quality Control – HPLC / GC

Roles & Experience

• Officer – 5 to 7 Years
• Executive – 8 to 10 Years

Qualification

• M.Sc – Chemistry

Technical Skills

• HPLC & GC instrumentation
• Analytical testing
• API quality analysis

Quality Assurance – QMS / AQA

Roles & Experience

• Chemist – 3 to 4 Years
• Officer – 5 to 7 Years
• Executive – 8 to 10 Years

Qualification

• M.Sc – Chemistry

Exposure

• QMS documentation
• Audit & compliance
• Process quality systems

 Safety – Shift Safety Officer

Experience

• 5 to 7 Years

Qualification

• B.Tech / M.Tech – Chemical
  OR
• Diploma – Industrial Safety

 Note

• Mentioned qualifications are mandatory
• API Pharma experience required

 Documents

• Updated Resume
• Educational Certificates
• Experience Letters
• ID Proof
• Passport Photos

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