QA Executive (IPQA) Jobs in Eugia Pharma Specialties Limited - Hyderabad, Telangana

QA Executive (IPQA) Jobs in Eugia Pharma Specialties Limited - Hyderabad, Telangana

work outline icon1 - 3 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Eugia Pharma Specialties Limited

time outline iconHyderabad, Telangana, India

Posted on 16-04-2026

1 Vacancy

Description

  • Job Title: QA Executive (IPQA)
  • Qualification: BPharm/MPharm
  • Location: Eugia Pharma Specialties Limited - Hyderabad, Telangana
  • Work Experience: 1 to 3 Years

Job Description

  • Implement and maintain Quality Management Systems (QMS).
  • Prepare, review, and control quality documents (SOPs, BMR, BPR).
  • Ensure compliance with GMP, GLP, and regulatory guidelines.
  • Handle deviations, CAPA (Corrective and Preventive Actions), and change control.
  • Conduct internal audits and support external/regulatory inspections.
  • Review batch records and ensure proper documentation.
  • Monitor production and quality processes for compliance.

Take this opportunity to join Eugia Pharma Specialties Limited - Hyderabad, Telangana as a QA Executive (IPQA) 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 Assurance (QA)

Preferred Education

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

Key Skills

Attention to DetailDocumentationAnalytical SkillsProblem Solving Skills

About Organization

Eugia Pharma Specialties Limited is a pharmaceutical organization engaged in the development and manufacturing of high-quality formulations, particularly injectables and specialty medicines, with a strong focus on innovation, regulatory compliance, and global standards. The role involves working in a manufacturing or operational environment to support production processes and ensure adherence to industry regulations. Responsibilities include assisting in production activities, monitoring process parameters, maintaining accurate batch records and documentation, and ensuring compliance with safety, hygiene, and environmental guidelines. The role also requires coordination with quality assurance and quality control teams, following Good Manufacturing Practices (GMP), and contributing to consistent product quality and operational efficiency.

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