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Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing  organization (CDMO), offering end-to-end development and manufacturing  solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.  

This enables us to offer a comprehensive range of services including Drug Discovery  Solutions, Process & Pharmaceutical Development services, Clinical Trial  Supplies, Commercial supply of APIs and Finished dosage forms. We also offer  specialized services like development and manufacture of Highly Potent APIs  and Antibody Drug Conjugation.  

Our capability as an integrated service provider  & experience with various technologies enables us to serve Innovator and  Generic companies worldwide.  

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Technical Staff

Job Description

Handles minor parametric setting issues in various machines and products.
Monitors the speed of the machine and output according to the run time.
Monitors and reports the unauthorized movement of workmen from line.
Takes up the responsibilities of the immediate supervisor for the section in his absence.
Helps the section in charge for preparing of SOP and other GMP documents.
Reports on day-to-day basis activities in SAP system. (If SAP user ID is available)
Verification/calibration of balances/Timer/Thickness gauge/S S Tablets/Lux meter etc on daily/monthly or as and when
Participate in machine qualification activities as per Qualification protocol whenever required.
Check all the calibration/qualification tags of equipment, instruments, or fire extinguishers for their due date from time to
Checking of line clearance during product changeover and batch changeover/ Monitoring of Temperature and RH/Press
Gradient of the area/area cleaning and disinfections

Allocates workmen for different workstations on a shift-to-shift basis.

Supervise/Line operations like weight verification, Tablet counting, Light intensity by lux meter, Challenge test /Camera teaching etc.in inspection area.

Review the batch manufacturing record and other quality documents.

Fills in process parameters, Batch manufacturing record (BMR) and GMP documents/record where required by following ALCOA+ principles.

Ensure no stoppage of operation/machines due to non-availability of manpower and any machine breakdown.