Quality Assurance Trainee

Evoke HR

AhmedabadFresher1h agovia Naukri

This job at a glance

Who can apply
Freshers and up to 1 year · B.Pharm
Must know
OperationsAuditing
Work
On-site in Ahmedabad
Pay
Not stated by the employer.
Skill demand
Auditing37%Operations15%of 99 similar fresher jobs posted in India this week
Listed
2 Nov 2026 · still open

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About the Role

We are looking for a motivated and detail-oriented Quality Assurance Trainee to support quality management activities in pharmaceutical and biotechnology operations. The candidate will assist in monitoring manufacturing processes, reviewing documentation, maintaining quality records, and ensuring compliance with industry standards and regulatory guidelines. This role provides an opportunity to gain practical experience in pharmaceutical quality assurance systems and Good Manufacturing Practices.

Key Responsibilities

  • Assist in implementing and maintaining quality assurance procedures and systems.
  • Review batch manufacturing records and batch packaging records for accuracy and completeness.
  • Support the preparation, review, and maintenance of Standard Operating Procedures (SOPs).
  • Monitor manufacturing and packaging activities to ensure compliance with quality standards.
  • Assist in maintaining documentation related to deviations, change controls, and corrective and preventive actions (CAPA).
  • Participate in internal quality audits and compliance assessments.
  • Support investigation and documentation of quality-related issues.
  • Ensure adherence to Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).

Qualifications & Skills

  • Bachelor's or Master's degree in Pharmacy (B.Pharm / M.Pharm), Pharmaceutical Sciences, Biotechnology, Microbiology, Chemistry, or related disciplines.
  • Fresh graduates interested in pharmaceutical quality assurance are encouraged to apply.
  • Basic understanding of pharmaceutical manufacturing and quality management systems.
  • Quality assurance and documentation.
  • Knowledge of GMP and GDP guidelines.
  • SOP preparation and document control.
  • Batch record review.
  • Understanding of deviation management and CAPA.
  • Basic knowledge of pharmaceutical manufacturing processes.

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