QA Officer Jobs in Siflon Drugs & Pharmaceuticals Pvt Ltd - Hyderabad, Telangana

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QA Officer Jobs in Siflon Drugs & Pharmaceuticals Pvt Ltd - Hyderabad, Telangana

work outline icon1 - 2 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Siflon Drugs & Pharmaceuticals Pvt Ltd

time outline iconHyderabad, Telangana, India

Posted on 21-04-2026

1 Vacancy

Description

  • Job Title: QA Officer
  • Qualification: BPharm/MPharm
  • Location: Siflon Drugs & Pharmaceuticals Pvt Ltd - Hyderabad, Telangana
  • Work Experience: 1 to 2 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 Siflon Drugs & Pharmaceuticals Pvt Ltd - Hyderabad, Telangana as a QA Officer 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 SkillsTeamwork

About Organization

Siflon Drugs & Pharmaceuticals Pvt Ltd is a pharmaceutical organization engaged in the manufacturing of veterinary formulations and animal healthcare products with a strong focus on product quality, regulatory compliance, and efficient production processes. The role involves working in a manufacturing or operational environment to support production activities and ensure adherence to industry standards. Responsibilities include assisting in production processes, 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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