A Production Chemist Documentation role focuses on meticulously
recording, managing, and reviewing all manufacturing data
, ensuring compliance with GMP/ISO, generating/approving batch records, SOPs, and quality reports, troubleshooting deviations via documentation analysis (CAPAs), and training staff on proper documentation, all to guarantee product quality, safety, and regulatory adherence in chemical/pharma production.
EXPERIENCE - 1 TO 3 YEAR WORKING EXPERIENCE IN API AND INTERMMEDIATE PLANT HAVING A GOOD GMP KNOWLEDGE.
Documentation Management:
Maintain accurate Batch Manufacturing Records (BMRs), production logs, equipment logs, cleaning records, and quality reports.
Quality & Compliance:
Ensure all activities follow GMP, ISO, and company SOPs; review/approve documents; support audits.
Process Oversight:
Monitor production, perform in-process checks, and coordinate with QC/QA for testing.
Troubleshooting & CAPA:
Investigate production deviations, analyze root causes (CAPAs), and implement corrective/preventive actions.
SOP/Procedure Development:
Develop, validate, and update Standard Operating Procedures (SOPs) and batch instructions.
Training & Support:
Train production staff on procedures and proper documentation practices.