Quality Control Executive

Company Description Sujata Nutri Pharma Pvt Ltd is a manufacturing company specializing in bulk drugs and food/pharma raw materials, located in G.I.D.C Road, Vadodara, Gujarat, India. The company focuses on providing reliable, quality-driven ingredients for pharmaceutical and nutrition-related applications. With a growing presence in the industry, it emphasizes consistency, regulatory compliance, and customer satisfaction.

Team members work in a manufacturing environment where safety, quality, and process discipline are core priorities. The organization offers opportunities to contribute to critical supply chains in healthcare and nutrition sectors. Role Description The Quality Control Executive is a full-time, on-site role based in Vadodara, responsible for ensuring that raw materials, in-process samples, and finished products meet established quality standards and regulatory requirements.

Day-to-day activities include performing routine and non-routine laboratory tests, recording and analyzing data, and preparing test reports in accordance with standard operating procedures (SOPs). The role involves monitoring and maintaining laboratory equipment, assisting with method validation, and supporting investigations of non-conformities or deviations. The Quality Control Executive will collaborate closely with production and quality assurance teams to resolve quality issues, support continuous improvement initiatives, and maintain proper documentation for audits and inspections.

The position requires adherence to safety protocols, good laboratory practices (GLP), and company policies at all times. Qualifications Strong Analytical Skills to interpret test results, troubleshoot issues, and support data-driven decisions. Hands-on Quality Control experience, including testing of raw materials, intermediates, and finished products.

Practical Laboratory Skills, including handling instruments, following SOPs, and maintaining accurate records. Knowledge of Quality Assurance principles, documentation practices, and compliance with relevant standards and guidelines. Experience with Calibration and routine maintenance of laboratory instruments to ensure accuracy and reliability.

Degree or diploma in Pharmacy, Chemistry, Microbiology, or a related scientific discipline. Familiarity with GMP, GLP, and regulatory requirements applicable to pharma or bulk drug manufacturing. Attention to detail, strong organizational abilities, and capacity to work effectively in a team-based, on-site environment.

Basic computer skills for data entry, report preparation, and use of laboratory or quality management software.