QA Executive (Validations) Jobs in Aurobindo Pharma Limited - Jadcherla, Telangana

institute logo

QA Executive (Validations) Jobs in Aurobindo Pharma Limited - Jadcherla, Telangana

work outline icon3 - 8 Years of Experiencerupess outline iconNot disclosed time outline iconPart Time

Aurobindo Pharma Limited

time outline iconJadcherla, Telangana, India

Posted on 27-04-2026

1 Vacancy

Description

  • Job Title: QA Executive (Validations)
  • Qualification: BPharm/MPharm
  • Location: Aurobindo Pharma Limited - Jadcherla, Telangana
  • Work Experience: 3 to 8 Years

Job Description

  • Review and approve batch manufacturing records (BMR), batch packing records (BPR), and other GMP documents.
  • Ensure implementation and compliance of Quality Management Systems (QMS) across departments.
  • Handle and review deviations, change controls, CAPA, and incident investigations.
  • Conduct internal audits, self-inspections, and support regulatory inspections.
  • Ensure data integrity and compliance with GMP, GDP, and regulatory guidelines.

Take this opportunity to join Aurobindo Pharma Limited - Jadcherla, Telangana as a QA Executive (Validations) 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

Problem Solving SkillsAnalytical SkillsDocumentationAttention to Detail

About Organization

Aurobindo Pharma Limited is a leading pharmaceutical company engaged in the manufacturing and development of high-quality medicines and formulations for global markets. The company operates advanced production facilities and follows strict regulatory and quality standards. The role involves supporting tablet compression production activities and ensuring smooth manufacturing operations. Responsibilities include operating and monitoring compression machines, maintaining batch records, and following SOP and GMP guidelines. The position focuses on efficient production processes, product quality, and maintaining pharmaceutical compliance standards.

Aggregated job.

Learn more