QA/QC Executive

Sujata Nutri Pharma; Vadodara; On-site; INR 300,000 - 500,000; Full time

Job summary

Sujata Nutri Pharma in Vadodara is seeking a QA/QC Executive with 2–3 years of experience. The candidate will be responsible for quality assurance and control, ensuring compliance with GMP, GLP, and regulatory standards.

Key responsibilities include conducting inspections and maintaining quality documentation. Ideal candidates will have strong analytical skills, attention to detail, and the ability to work in a regulated environment. Proficiency in MS Office is required.

Qualifications

• 2-3 years of experience in QA/QC.
• Understanding of GMP, GLP, FDA, and ISO standards.
• Ability to work in a regulated laboratory environment.

Responsibilities

• Perform quality assurance and quality control activities as per company procedures.
• Review batch manufacturing records and quality documentation.
• Conduct raw material, in-process, and finished product inspections/testing.

Skills

Knowledge of QA/QC processes and quality management systems

Good analytical and problem-solving skills

Attention to detail and accuracy in documentation

Proficiency in MS Office applications

Tools

Laboratory instruments and microbiological equipment

Job description

We are seeking a motivated and detail-oriented QA/QC Executive with 2–3 years of experience to join our team in Vadodara. The candidate will be responsible for ensuring product quality, maintaining quality systems, conducting testing activities, and supporting compliance with regulatory and GMP requirements.

Key Responsibilities

• Perform quality assurance and quality control activities as per company procedures.
• Review batch manufacturing records, analytical reports, and quality documentation.
• Conduct raw material, in-process, and finished product inspections/testing.
• Ensure compliance with GMP, GLP, SOPs, and regulatory requirements.
• Investigate deviations, non-conformances, OOS, and customer complaints.
• Prepare and maintain QA/QC documentation, reports, and records.
• Support internal audits, vendor audits, and regulatory inspections.
• Monitor CAPA implementation and effectiveness.
• Coordinate with production, warehouse, and other departments to resolve quality-related issues.
• Ensure adherence to Good Documentation Practices (GDP).

Qualifications

• Knowledge of QA/QC processes and quality management systems.
• Understanding of GMP, GLP, FDA, and ISO standards.
• Good analytical and problem-solving skills.
• Attention to detail and accuracy in documentation.
• Ability to work in a regulated laboratory environment.
• Experience with laboratory instruments and microbiological equipment is an advantage.
• Familiarity with deviation, OOS, change control, and CAPA processes.
• Proficiency in MS Office applications.
• Required experience: 2–3 years in QA/QC.
• Location: Vadodara.
• Working hours: 10:00 AM – 06:30 PM.