QA Trainee Jobs in Fermenta Biotech Ltd - Bharuch, Gujarat

QA Trainee Jobs in Fermenta Biotech Ltd - Bharuch, Gujarat

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

Fermenta Biotech Ltd

time outline iconBharuch, Gujarat, India

Posted on 09-04-2026

1 Vacancy

Description

  • Job Title: QA Trainee
  • Qualification: BPharm/MPharm
  • Location: Fermenta Biotech Ltd - Bharuch, Gujarat
  • 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 Fermenta Biotech Ltd - Bharuch, Gujarat as a QA Trainee in Bharuch, 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)

Preferred Education

MPharm (Master Of Pharmacy)BPharm (Bachelor Of Pharmacy)

Key Skills

TeamworkDocumentationProblem Solving SkillsCommunication Skills

About Organization

Fermenta Biotech Ltd is a biotechnology and pharmaceutical organization engaged in the manufacturing of specialty chemicals and active pharmaceutical ingredients with a strong focus on quality, safety, and regulatory compliance. 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 documentation and batch records, and ensuring compliance with safety and environmental guidelines. The role also requires coordination with quality assurance and quality control teams, following Good Manufacturing Practices (GMP), and contributing to efficient and consistent production operations.

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