Executive/Sr. Executive-QA (IPQA) Jobs in Aurobindo Pharma Limited - Jadcherla, Telangana

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Executive/Sr. Executive-QA (IPQA) Jobs in Aurobindo Pharma Limited - Jadcherla, Telangana

work outline icon0 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Aurobindo Pharma Limited

time outline iconJadcherla, Telangana, India

Posted on 01-06-2026

1 Vacancy

Description

  • Job Title: Executive/Sr. Executive-QA (IPQA)
  • Qualification: BPharm (Bachelor Of Pharmacy)
  • Location: Aurobindo Pharma Limited - Jadcherla, Telangana
  • Work Experience: 0 to 5 Years

Job Description

  • Implement and maintain quality assurance systems as per company and regulatory standards.
  • Review and approve batch manufacturing records and quality documentation.
  • Conduct internal audits to ensure compliance with GMP and quality guidelines.
  • Monitor production and quality processes to ensure product quality and consistency.
  • Investigate deviations, non-conformances, and implement corrective and preventive actions (CAPA).
  • Coordinate with production, QC, and other departments for quality-related activities.

Take this opportunity to join Aurobindo Pharma Limited - Jadcherla, Telangana as a Executive/Sr. Executive-QA (IPQA) 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

BPharm (Bachelor Of Pharmacy)

Key Skills

Decision-Making SkillsLeadership SkillsSelf-motivationCommunications Skills

About Organization

Aurobindo Pharma Limited is a leading pharmaceutical manufacturing company focused on developing, manufacturing, and marketing high-quality generic medicines, active pharmaceutical ingredients (APIs), and specialty healthcare products with an emphasis on innovation, regulatory compliance, and global quality standards. The role involves working in a professional pharmaceutical manufacturing environment to support production, quality assurance, quality control, research and development, regulatory affairs, supply chain, and operational activities. Responsibilities include maintaining GMP compliance, handling technical and quality documentation, coordinating with cross-functional teams, monitoring manufacturing and quality processes, and supporting efficient plant operations. The role also requires strong analytical skills, teamwork, adherence to regulatory guidelines, and commitment to delivering safe, effective, and high-quality pharmaceutical products.

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