Job Description

Key Responsibilities:

Prepare, review, and maintain QC test reports, batch analysis records, COAs (Certificates of Analysis), and inspection logs. Ensure timely documentation of all laboratory testing activities (raw materials, in-process, and finished products). Maintain and update SOPs, Work Instructions, and Specifications related to quality control. Ensure proper filing, archiving, and retrieval of all QC documents (manual and electronic). Maintain and verify instrument calibration and validation records. Coordinate with the QA department for document issuance, control, and change management. Prepare and compile quality data for internal and external audits. Ensure all records comply with ISO, KOSHER , or HALAL and customer audit requirements. Assist QC chemists and analysts in proper documentation of lab results. Support audit readiness and participate in customer or regulatory inspections. Ensure traceability and integrity of analytical data and records.
Qualifications & Experience:

B.Sc. / M.Sc. in Chemistry, Industrial Chemistry, Chemical Engineering, or related field. 2 +years of experience in QC or documentation in a chemical, dyes, pigments, or food colour manufacturing industry. Knowledge of Good Documentation Practices (GDP) and Good Laboratory Practices (GLP). Familiarity with MSDD (material safety data sheep), ISO, KOSHER , or HALAL systems preferred. Experience with ERP Software, or electronic documentation systems is an advantage.
Job Type: Full-time

Pay: ₹20,000.00 - ₹25,000.00 per month

Experience:

Chemical Industry: 1 year (Preferred) Documentation review: 1 year (Preferred) Documentation Practices (GDP): 1 year (Preferred) Laboratory Practices (GLP): 1 year (Preferred)
Work Location: In person