QA Trainee Jobs in Viyash Scientific Ltd - Nalgonda, TelanganaExecutive qu

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QA Trainee Jobs in Viyash Scientific Ltd - Nalgonda, TelanganaExecutive qu

work outline icon0 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Viyash Scientific Ltd

time outline iconNalgonda, Telangana, India

Posted on 24-04-2026

1 Vacancy

Description

  • Job Title: QA Trainee
  • Qualification: BSc/MSc Chemistry
  • Location: Viyash Scientific Ltd - Nalgonda, Telangana
  • Work Experience: 0 to 5 Years

Job Description

  • Assist in implementing and maintaining Quality Management Systems (QMS).
  • Support preparation, review, and control of quality-related documents (SOPs, BMR, BPR).
  • Participate in internal audits and regulatory inspections.
  • Monitor production and quality processes to ensure compliance with standards.
  • Assist in deviation handling, CAPA (Corrective and Preventive Actions), and change control.
  • Ensure adherence to GMP (Good Manufacturing Practices) guidelines.
  • Maintain records and documentation as per regulatory requirements.

Take this opportunity to join Viyash Scientific Ltd - Nalgonda, Telangana as a QA Trainee in Nalgonda, 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

BSc ChemistryMSc Chemistry

Key Skills

Problem Solving SkillsDocumentationTeamworkCommunication Skills

About Organization

Viyash Scientific Ltd is a pharmaceutical manufacturing organization committed to delivering high-quality products with a strong focus on innovation, regulatory compliance, and advanced healthcare solutions. The role involves working in a manufacturing and research-driven environment to support production processes and ensure smooth functioning of operations. Responsibilities include assisting in production activities, coordinating with Quality Control (QC), Quality Assurance (QA), and R&D teams, maintaining accurate documentation, and following standard operating procedures (SOPs). The role also requires strict adherence to Good Manufacturing Practices (GMP), regulatory guidelines, and safety standards across departments. It involves monitoring manufacturing processes, ensuring proper handling of materials, supporting quality checks, and maintaining hygiene and safety in the production area.

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