Review and check the raw data generated under his supervision.
Plan and distribute the daily routine work.
To assist analyst for trouble shooting of instrumental problems.
To ensure availability of reference and working standards.
To ensure that all instruments are calibrated as per schedule.
To maintain instrument parts, columns, etc.
Review and maintain the logbooks, COAs, specifications and test procedures related to his section responsibility.
Analysis and approval of cleaning validation / verification samples.
Release/Rejection of products and materials and issue of release or rejection labels.
Approving of receiving logbook.
Report to QC Manager about the out of specification results obtained in routine analysis and retesting in order to perform proper investigation to verify the deviation.
To ensure the approved procedures and specifications are followed.
To check the artwork forwarded by R&D.
Perform proper training for employees.
Perform trend analysis.
Signing off on COA etc.
To ensure availability of adequate media, reagents, glassware and solutions.
To ensure preparation and sterilization of media and documentation for preparation of media as per designed procedure.
To ensure proper maintenance of media stock.
To ensure disposition of samples and used media.
To perform developmental activities.
Maintain proper control for raw material supplier’s qualification program.
Performing required risk approach for all critical tests (Heavy metals, Residual Solvents ,…etc.).
To be aware about pharmacopeia analytical requirements.
Has long experience for different analytical techniques.
Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.