QA Officer (API) Jobs in BDR Pharmaceuticals Internationals Pvt Ltd - Vadodara, Gujarat

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QA Officer (API) Jobs in BDR Pharmaceuticals Internationals Pvt Ltd - Vadodara, Gujarat

work outline icon2 - 6 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

BDR Pharmaceuticals Internationals Pvt Ltd

time outline iconVadodara, Gujarat, India

Posted on 16-04-2026

1 Vacancy

Description

  • Job Title: QA Officer (API)
  • Location: BDR Pharmaceuticals Internationals Pvt Ltd - Vadodara, Gujarat
  • Work Experience: 2 to 6 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.

Take this opportunity to join BDR Pharmaceuticals Internationals Pvt Ltd - Vadodara, Gujarat as a QA Officer (API) in Vadodara, Gujarat 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)

Key Skills

DocumentationProblem Solving SkillsCoordination SkillsAttention to Detail

About Organization

BDR Pharmaceuticals Internationals Pvt Ltd is a pharmaceutical organization engaged in the manufacturing of active pharmaceutical ingredients (APIs) and formulations, with a strong focus on oncology, critical care, and specialty medicines. 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, 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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