·         To ensure proper sampling as per sampling plan by day to day monitoring of receipt of raw material as per production requirement  

·         Checking of sampling report with entry of raw material in register.

·         To ensure the distribution of sample to related section for analysis work

·         Every day meeting with production and supply chain people for the requirement as per production plan

·         Distribution of work to the chemist and executives as per the production priority .

·         To issue the signed protocol along with sample to related chemist.

·         To check the chemist working place during analysis and solve problem if required.

·         To check raw data of approved material .

·         Material is rejected OOS will be followed it .

·         To ensure the approved/rejected sticker pasted on every container as per SOP.

·         To check and approve certificate of analysis of raw material.

·         To visit warehouse daily for an hour to check the activity related to QC.

·         To ensure availability of SOP.

·         To check and upgrade the standard test procedure as per pharmacopoeia change

·         To prepare the raw protocol for the raw materials.

·         To check and ensure the calibration record as per annual calibration schedule.

·         To prepare justification for instruments as per requirements.

·         Preparation of IQ, OQ and PQ for the  installed instruments .

·         To monitor and update the annual maintenance contract of all the instrument.

·         Responsible for the investigation for OOS as on required.

·         Responsible for the updation of vendor list as per the SOP

• To train and validate the chemist for the analysis work.
• Training of SOP as per the training schedule .
• Arranging the training and troubleshooting session of the instrument from the instrument application engineer for related instrument.

To train the chemist for GLP aspects in Laboratory.

Please share your CVs at annie@maxpeoplesolution.com