21 Aug
|
Itpharmasource
|
Chhindwara
21 Aug
Itpharmasource
Chhindwara
We are seeking an experienced QC Chemist with 3–5 years of experience in the pharmaceutical or Ayurvedic pharmaceutical manufacturing industry, with robust exposure to quality control documentation systems and regulatory compliance practices. The candidate should have hands-on experience in GC and HPLC analysis, along with in-depth knowledge of QC instruments, laboratory documentation, and GMP-compliant record management. The role involves ensuring product quality, performing analytical testing, and maintaining complete and accurate documentation as per regulatory standards.
Key Responsibilities
- Perform routine and non-routine analysis of raw materials, in-process samples, and finished products as per approved specifications and SOPs.
- Operate and handle QC instruments including HPLC, GC, UV, FTIR, pH meter, and other laboratory equipment.
- Conduct GC and HPLC analysis for qualitative and quantitative testing and ensure proper documentation of all chromatographic data.
- Maintain and update laboratory notebooks, analytical worksheets, raw data records, instrument usage logs,
and electronic documentation systems (if applicable).
- Ensure compliance with GMP, GLP, and regulatory documentation practices in all QC activities.
- Prepare, verify, and maintain COA (Certificate of Analysis), analytical reports, and batch-wise quality documentation.
- Perform calibration, qualification, and verification of laboratory instruments as per approved schedules and maintain proper records.
- Identify deviations, document observations, and support OOS (Out of Specification) and OOT investigations with complete traceability of data and records.
- Assist in method validation, method transfer, and stability studies, ensuring all supporting documentation is complete, accurate, and audit-ready.
- Ensure proper documentation for handling, storage, and disposal of chemicals, reagents, and laboratory waste as per SOPs.
- Support internal and external audits by ensuring readiness of QC
📌 QC hplc + Documentation (Chhindwara)
🏢 Itpharmasource
📍 Chhindwara