QC Officer

Drlogy; Vadodara; On-site; INR 350,000 - 550,000; Full time

Job summary

Drlogy is seeking a QC Officer to oversee quality control activities in Vadodara, India. The role involves performing analytical testing on raw materials, in-process samples, and finished products while ensuring compliance with GLP and GMP standards. Candidates should possess strong analytical skills and the ability to maintain thorough documentation. The position offers an opportunity to collaborate with QA and production teams to enhance product quality and operational efficiency.

Qualifications

• Strong understanding of analytical testing methods.
• Familiarity with quality control standards and practices.
• Ability to perform calibration and maintenance of QC instruments.

Responsibilities

• Perform analytical testing of raw materials and finished products.
• Ensure compliance with GLP, GMP, and quality standards.
• Maintain accuracy in laboratory records and documentation.
• Coordinate with QA and production for quality activities.

Skills

Analytical testing

GLP/GMP compliance

Laboratory instruments operation

Document management

Quality assurance

Tools

Laboratory equipment

Job description

The QC Officer will be responsible for performing quality control activities related to raw materials, in-process samples, packaging materials, and finished products. The involves conducting analytical testing, maintaining laboratory documentation, ensuring compliance with GLP/GMP standards, and supporting continuous quality improvement initiatives. The candidate will work closely with QA, production, and regulatory teams to maintain high product quality and operational efficiency.

• Perform analytical testing of raw materials, in-process samples, and finished products.
• Ensure accurate and timely testing as per approved specifications and SOPs.
• Operate and maintain laboratory instruments and analytical equipment.
• Perform calibration and routine maintenance of QC instruments.
• Prepare and maintain laboratory records, reports, and documentation accurately.
• Ensure compliance with GLP, GMP, and regulatory quality standards.
• Review analytical data and report any out-of-specification (OOS) results.
• Support investigation of deviations, OOS, and quality-related issues.
• Monitor and maintain laboratory inventory including chemicals, reagents, and standards.
• Ensure proper labeling, storage, and handling of laboratory materials.
• Coordinate with QA and production teams for quality-related activities.
• Participate in method validation, method transfer, and stability studies as required.
• Maintain cleanliness, safety, and organization of the laboratory environment.
• Ensure adherence to SOPs, safety guidelines, and company policies.
• Support internal audits, external audits, and regulatory inspections.
• Maintain data integrity and confidentiality of laboratory information.
• Prepare MIS reports and testing summaries for management review.
• Assist in continuous improvement initiatives within QC operations.
• Stay updated with analytical techniques, regulatory updates, and industry best practices.
• Ensure timely release of materials and products based on quality evaluation.