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Safety Knowledge:- Material Safety Data Sheet (MSDS), General Laboratory Safety.

Primary Knowledge:- Ensure Compliance with cGMP, GDP, GLP, data integrity and Safety principles within the section. Quality Valuable Manufacturing practices, Good Documentation Practices, Data integrity, Standard Operating Procedure, Specifications, Contamination, Cross-contamination, Least count, Workplace monitoring, Gowning, degowning, Valuable Laboratory Practices.

Instrument Handling & Analytical Practice: Pipetting, Analytical Balance, Wet Chemistry, P/W, Titimetry Analysis, pH Meter & It's Measurements, pH Meter & It's Measurements, Water Analysis, Specific Gravity, Conductivity Meter, Raw Material Sampling and Analysis, Particle Size Analysis (PSD) & BD, TD and Moisture Content, Refractometer, Thin Layer Chromatography, UV Spectrophotometer, Assay, Melting Point and Boiling Point, LOD & ROI, KF Titration, IR, Tablet Friability, Hardness and Physical Parameters, Disintegration Test Apparatus, Dissolution Test Apparatus, QMS, Stability, HPLC, GC.

Role & responsibilities :-
Ensure Compliance with cGMP, GDP, GLP, data integrity and Safety principles within the section.
Responsibility of laboratory safety and to carry out the work with safety norms.
Handling of laboratory Instruments/ Equipment's and Glassware,



Chemicals, reagents, etc.
Prepared of certificate of analysis for Intermediate, raw material, Recovered Solvents / Substances , By product, In-Process ,Purified/Potable/ Treated water and etc.
Compliance of all QC related activities & SOPs/GTPs.
Performed analysis of Analytical method validation/ verification/ method Transfer , analytical cleaning validation, Intermediate, Raw material, Recovered Solvents / Substances , By product, , In process, Purified/Potable/ Treated water and etc., for HPLC related activity performed
Handling of working /references standard Qualification Data.
Maintain instrument/equipment usage logbook.
Timely reporting of any incident, Lab event, OOS, OOT result to the Section Head.
To perform the transaction in ERP, Trackwise, Caliber DMS, PLMS and Mac Portal software as per authorization rights.
Ensure require trainings & qualification is successfully completed before allocating/ assigning the activity QC employee.
Arrangement of documents (SOPs, Specifications and STPs, etc.).
Performed of equipment / instrument qualification and calibration related activity.
Handling the trouble shooting of all QC instruments/ Equipment.

📌 Qc Officer/sr Officer Dahej
🏢 Macleods Pharmaceuticals
📍 Dahej