About the company
Baxter one of the top Pharmaceutical and medical devices company, with the head quarters located in Illinois. Primary focus of treatment for the company is in the area of Hemophilia and in treating the immune and chronic medical conditions. The firm relieves the issues for millions of patients across the globe serving to the man kind from more than 85 years.
In the year 2018 Baxter was awarded for the best place to work globally. The company have the portfolio of medicines in Critical care, Nutritional, renal care, surgical and Hospital care. Apart from the pharmaceutical medicines the company also provides medical devices and infusions.
About the Job
Location of the Job : Ahmedabad, Gujarat
Able to perform CIP&SIP process as per the validated processor
Required to have strong knowledge on clean hero procedure Unable to update the entry and exit procedures
Need to implement the current good manufacturing practices in the production area
Able to verify the equipment in the production area and perform prevent to maintenance if found any abnormality And resolve as per the standard operating procedure
able to follow the standard operating procedures and adhere to it and update them
Required to ensure the availability of patch manufacturing records During audits and submit the execute BMR
Continuously monitor the temperature humidity and pressure of clean rooms Escalate if deviated from the acceptance criteria and inform to engineering department to rectify as per the SOP
Any abnormalities observed during the batch manufacturing should Informed to the supervisor and Perform the corrective action in a timely manner in line with standard operating procedure
Required to bear protective equipment while working with production area and during routine maintenance of production equipment as per SOP
Perform lockout handle tiger procedure for Critical equipment utilities To prevent the hazards
Monitor and ensure all the activities are carried out in compliance mode
Need to have knowledge on good manufacturing practices and for Good documentation and standard operating procedure and data integrity principles
Required to ensure that current could manufacturing practices are being followed and maintained across the production
Immediately stop the activity if any nonconformance found and informed to supervisor for proper resolution As per the standard operating procedure
Able to take the responsibility of chemist or operator in the absence of supervisor