Jr. Executive / Executive-QC Jobs in Hetero Drugs Limited - Jadcherla, Telangana

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Jr. Executive / Executive-QC Jobs in Hetero Drugs Limited - Jadcherla, Telangana

work outline icon2 - 9 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Hetero Drugs Limited

time outline iconJadcherla, Telangana, India

Posted on 11-03-2026

1 Vacancy

Description

  • Job Title: Jr. Executive / Executive-QC
  • Qualification: BPharm/MPharm
  • Location: Hetero Drugs Limited - Jadcherla, Telangana
  • Work Experience: 2 to 9 Years

Job Description

  • Perform routine quality control testing of raw materials, in-process samples, and finished products.
  • Conduct analytical testing using instruments such as HPLC, GC, UV, and other laboratory equipment.
  • Ensure all testing activities comply with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
  • Prepare and maintain laboratory documentation, test reports, and analytical records.
  • Review analytical data and ensure results meet quality specifications.
  • Assist in investigation of out-of-specification (OOS) results and deviations.

Take this opportunity to join Hetero Drugs Limited - Jadcherla, Telangana as a Jr. Executive / Executive-QC in Jadcherla, 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

MPharm (Master Of Pharmacy)BPharm (Bachelor Of Pharmacy)

Key Skills

DocumentationAnalytical SkillsProblem Solving SkillsAttention to Detail

About Organization

Hetero Drugs Limited is a leading pharmaceutical company known for manufacturing high-quality medicines and injectable formulations for global markets. The company operates advanced production facilities and follows strict regulatory and quality standards. The role involves operating and monitoring injectable production equipment in the manufacturing unit. Responsibilities include maintaining batch records, following SOP and GMP guidelines, and ensuring proper production processes. The position focuses on efficient manufacturing operations, product quality, and maintaining pharmaceutical safety standards.

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