Monitoring & ensuring implementation of current GMP & GLP norms in Manufacturing Unit of Antiseptics, Disinfectants & Sterilization Products liquid forms.
Training, framing the documentation for Q.C departments (SOPs / STPs, protocols, and various other GMP records) and complete responsibility for Regulatory Compliance.
Must have experience in handling instruments like UV-VIS, Wet Lab, chemical analysis of Raw Materials, finished products & Packing materials.
Calibrating, maintaining analytical Instruments.
Employement Category:
Employement Type: Full timeIndustry: Pharma / BiotechRole Category: Quality (QA-QC)Functional Area: Not ApplicableRole/Responsibilies: Qc Manager