QA Officer Jobs in AXA Parenterals Ltd - Roorkee, Uttarakhand

QA Officer Jobs in AXA Parenterals Ltd - Roorkee, Uttarakhand

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

AXA Parenterals Ltd.

time outline iconRoorkee, Uttarakhand, India

Posted on 23-04-2026

1 Vacancy

Description

  • Job Title: QA Officer
  • Qualification: BPharm/MPharm
  • Location: AXA Parenterals Ltd - Roorkee, Uttarakhand
  • Work Experience: 1 to 4 Years

Job Description

  • Ensure all manufacturing activities comply with Good Manufacturing Practice (GMP) guidelines and internal quality standards.
  • Review and maintain quality documents such as SOPs, BMR (Batch Manufacturing Record), and BPR (Batch Packaging Record).
  • Monitor production processes to ensure product quality and regulatory compliance.
  • Handle quality-related documentation including deviations, change controls, and Corrective and Preventive Action (CAPA) reports.
  • Conduct in-process quality checks and support validation activities.

Take this opportunity to join AXA Parenterals Ltd - Roorkee, Uttarakhand as a QA Officer in Roorkee, Uttarakhand 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

TeamworkAttention to DetailDocumentationAnalytical Skills

About Organization

AXA Parenterals Ltd is a pharmaceutical manufacturing organization engaged in the production of sterile parenteral preparations, intravenous fluids, and life-saving medicines with a strong focus on product quality, regulatory compliance, and advanced manufacturing technology. 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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