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

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

work outline icon1 - 6 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-QA
  • Qualification: BPharm/MPharm
  • Location: Hetero Drugs Limited - Jadcherla, Telangana
  • Work Experience: 1 to 6 Years

Job Description

  • Review and approve Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
  • Ensure compliance with GMP, SOPs, and regulatory requirements.
  • Perform in-process quality checks (IPQA) and line clearance activities.
  • Handle deviations, CAPA, change controls, and incident investigations.
  • Support internal audits and regulatory inspections.
  • Maintain QA documentation and ensure data integrity practices.
  • Coordinate with Production, QC, and Warehouse teams for quality issues.
  • Monitor implementation of quality systems and continuous improvement activities.

Take this opportunity to join Hetero Drugs Limited - Jadcherla, Telangana as a Jr. Executive/Executive-QA 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 Assurance (QA)

Preferred Education

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

Key Skills

Attention to DetailTeam working SkillsProblem Solving SkillsCommunication Skills

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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