QA Officer Jobs in Ipca Laboratories - Daman, Dadra & Nagar Haveli and Daman & Diu

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QA Officer Jobs in Ipca Laboratories - Daman, Dadra & Nagar Haveli and Daman & Diu

work outline icon2 - 4 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Ipca Laboratories Limited

time outline iconDaman, Dadra & Nagar Haveli and Daman & Diu, India

Posted on 07-04-2026

1 Vacancy

Description

  • Job Title: QA Officer
  • Qualification: BPharm
  • Location: Ipca Laboratories - Daman, Dadra & Nagar Haveli and Daman & Diu
  • Work Experience: 2 to 4 Years

Job Description

  • Ensure compliance with GMP and quality assurance standards.
  • Review batch manufacturing records and quality documents.
  • Monitor production processes for quality compliance.
  • Handle deviations, CAPA, and change control documentation.
  • Conduct internal audits and quality inspections.
  • Coordinate with QC and production teams for quality issues.
  • Maintain QA documentation and quality records.
  • Support regulatory audits and quality improvement activities.

Take this opportunity to join Ipca Laboratories - Daman, Dadra & Nagar Haveli and Daman & Diu as a QA Officer in Daman, Dadra & Nagar Haveli and Daman & Diu 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

DocumentationProblem Solving SkillsCoordination SkillsAttention to Detail

About Organization

Ipca Laboratories is a well-established pharmaceutical organization engaged in the manufacturing of high-quality formulations with a strong focus on regulatory compliance, product quality, and efficient production operations. The role involves working in a manufacturing or operational environment to support production processes and ensure adherence to industry standards. Responsibilities include assisting in production activities, following Good Manufacturing Practices (GMP), maintaining accurate batch records and documentation, monitoring equipment and process performance, and ensuring compliance with safety and hygiene protocols. The role also requires coordination with quality assurance and quality control teams, adherence to regulatory guidelines, and maintaining consistency in product quality and operational efficiency.

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