Quality Assurance Trainee

Evoke HR; Ahmedabad District; On-site; INR 240,000 - 360,000; Full time

Job summary

Evoke HR Solutions Pvt. Ltd. invites applications for a Quality Assurance Trainee. This role supports quality management activities within pharmaceutical operations, focusing on GMP/GDP compliance, documentation control, and SOP maintenance.

The successful candidate will review batch records, assist in CAPA and deviation processes, and learn through hands-on exposure to manufacturing and quality systems in a fast-paced environment.

Qualifications

• Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, Biotechnology, Microbiology, Chemistry, or related disciplines.
• Fresh graduates encouraged to apply.
• Basic understanding of pharmaceutical manufacturing and quality management systems.

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 SOPs.
• Monitor manufacturing and packaging activities to ensure compliance with quality standards.
• Assist in maintaining documentation related to deviations, change controls, and CAPA.
• Participate in internal quality audits and compliance assessments.
• Support investigation and documentation of quality-related issues.
• Ensure adherence to GMP and GDP.

Skills

Quality assurance & documentation

GMP & GDP knowledge

SOP preparation & document control

Batch record review

Deviation management & CAPA

Pharmaceutical manufacturing basics

Education

B.Pharm / M.Pharm or related disciplines

Job description

Job Title: Quality Assurance Trainee
Department: Pharmaceutical & Biotechnology
Role: Pharmaceutical & Biotechnology Other
Experience: Fresher / 0–1 Year
Job Type: Full-Time

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).

Eligibility

• 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.

Required Skills

• 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.