Quality Control (Officer - Sr. Executive)

SPC Life Sciences Ltd.; Dahej; On-site; INR 450,000 - 750,000; Full time

Job summary

SPC Life Sciences Ltd. in Dahej, Gujarat, India, is seeking a QC professional to perform routine and specialized testing of raw materials, in-process, and finished products. You will operate HPLC, GC, and UV-Vis, validate methods, and maintain comprehensive documentation to ensure regulatory compliance.

The role involves supporting audits, CAPA investigations, and training junior staff, with a focus on data analysis and quality assurance in a GMP environment.

Qualifications

• Experience in routine and specialized testing of raw materials, in-process, and finished products.
• Knowledge of GLP, GMP regulatory requirements.
• Strong documentation and data analysis skills.
• Ability to train and support junior staff.
• Troubleshoot analytical equipment issues.

Responsibilities

• Perform routine and specialized testing of materials and products.
• Operate HPLC, GC, and UV-Vis instruments.
• Validate and calibrate analytical methods and equipment.
• Maintain accurate documentation of results, deviations, and observations.
• Ensure GLP/GMP compliance and participate in audits.
• Investigate deviations and implement CAPA.
• Prepare QC reports with trends and findings.
• Manage sample receipt, storage, and tracking.
• Develop and update SOPs and QC procedures.
• Train junior staff on QC practices.

Skills

HPLC

GC

UV-Vis

Documentation

CAPA

Tools

HPLC

GC

UV-Vis

Calibration

Job description

Role & responsibilities

• Perform routine and specialized testing of raw materials, in-process, and finished products.
• Operate analytical instruments such as HPLC, GC, and UV-Vis spectrophotometers.
• Validate and calibrate analytical methods and laboratory equipment.
• Maintain accurate documentation of test results, deviations, and observations.
• Ensure compliance with GLP, GMP, and regulatory requirements.
• Participate in internal audits and support external inspections.
• Investigate deviations, identify root causes, and implement corrective actions (CAPA).
• Analyze data and prepare QC reports with key findings and trends.
• Manage sample receipt, handling, storage, and tracking.
• Develop and update SOPs, QC procedures, and work instructions.
• Train and support junior staff on QC practices and equipment.
• Troubleshoot analytical and equipment-related issues.
• Stay updated with regulatory guidelines and industry standards.