Quality Control (Officer - Sr. Executive)

Spc Life Sciences; Dahej; On-site; INR 350,000 - 520,000; Full time

Job summary

Spc Life Sciences in Dahej, Gujarat, seeks a meticulous QC Analyst to perform routine and specialized testing of raw materials, in-process, and finished products, and to operate HPLC, GC, and UV-Vis spectrophotometers.

You will validate methods, maintain documentation, ensure GLP/GMP compliance, support audits, investigate deviations, prepare QC reports, manage samples, develop SOPs, train junior staff, and troubleshoot equipment.

Qualifications

• GLP/GMP compliance knowledge.
• Attention to detail and documentation skills.
• Ability to operate analytical instruments.

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.

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.