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What you'll do

• Well Verse with tablet/capsule inspection activity in non-sterile area on a shift-to-shift basis and to complete documentation in accordance with cGMP requirements.
• · To take training before executing any operation.
• · Fills in process parameters in Batch manufacturing record (BMR) and GMP documents.
• / Record where required by following ALCOA + principles.
• · Use self-login ID and password & do not share it to anyone.
• · Follow instruction for new machine/methodology in accordance with the quality standards.
• · Clean and check the equipment like tablet inspection machine (Belt type) /Automatic tablet and capsule inspection machine for Type A, B & D type in case of product / batch change and major mechanical related maintenance job.
• · Visually check for the absence of any residue of previous product or any extraneous matter after machine cleaning.
• · Do status labelling as per SOP and proper arrangement of Inspection area.
• · Calibrate the balances as per SOP whenever required.

Who can apply

• · Always maintain good hygienic at workplace/during working in manufacturing/inspection area.
• · Set the parameter of machine as defined in the Batch manufacturing record (BMR) and SOP.
• · Check and ensure that temperature, RH and differential pressure of inspection area shall be within limit .
• · To operate the inspection machine as instructed by shift supervisors.
• · In case of any non-conformity or deviation inform the line supervisor immediately.
• · Delivers the expected output as per run time of the machine.
• · Knowledge and involvement in EHS, SFTI,6S,ISO 14001 and ISO 13485 activities.
• · Address the minor mechanical issues in terms of machine setting from time to time and inform supervisor during any breakdown where maintenance helps are required.
• Any other activity from time to time which his supervisor/company feels appropriate.

About Piramal Pharma

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