QC Chemist (GC) Jobs in Neuland Laboratories Ltd - Hyderabad, Telangana

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QC Chemist (GC) Jobs in Neuland Laboratories Ltd - Hyderabad, Telangana

work outline icon3 - 7 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Neuland Laboratories Ltd

time outline iconHyderabad, Telangana, India

Posted on 30-05-2026

1 Vacancy

Description

  • Job Title: QC Chemist (GC)
  • Qualification: MSc Chemistry
  • Location: Neuland Laboratories Ltd - Hyderabad, Telangana
  • Work Experience: 3 to 7 Years

Job Description

  • Perform chemical and instrumental analysis of raw materials, intermediates, and finished products.
  • Conduct tests using instruments such as HPLC, GC, UV, IR, and titration methods.
  • Follow GLP (Good Laboratory Practices) and GMP (Good Manufacturing Practices) guidelines.
  • Prepare and maintain analytical reports and documentation.
  • Ensure proper calibration and maintenance of laboratory instruments.
  • Identify deviations, out-of-specification (OOS) results, and report to seniors.
  • Assist in method development and validation activities.

Take this opportunity to join Neuland Laboratories Ltd - Hyderabad, Telangana as a QC Chemist (GC) in Hyderabad, Telangana and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.

Category

Pharmaceuticals

Functional Area

Pharma Quality Control (QC)

Preferred Education

MSc Chemistry

Key Skills

Communication SkillsTeamworkAttention to DetailProblem Solving Skills

About Organization

Neuland Laboratories Ltd is a pharmaceutical company focused on the development and manufacturing of active pharmaceutical ingredients (APIs), specialty chemicals, and healthcare solutions with an emphasis on innovation, quality, and regulatory compliance. The role involves working in a professional pharmaceutical manufacturing environment to support production, quality assurance, research and development, regulatory affairs, and operational activities. Responsibilities include maintaining GMP compliance, handling technical and quality documentation, coordinating with cross-functional teams, monitoring manufacturing processes, and supporting efficient operational performance. The role also requires strong analytical skills, teamwork, adherence to regulatory standards, and commitment to delivering high-quality pharmaceutical products and services.

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