Openings for Sr. Executive in Manufacturing for Baxter

Openings for Sr. Executive in Manufacturing for Baxter

 

Baxter Logo

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 : 

Experience : Candidate need to have minimum experience of 1-3 years with handling or exposure in Sterile injectables 

Roles & Responsibilities : 


Able to Handle  that the maintenance of dispensing, including airlocks is as per SOP.

Thorough understanding on cross contamination and  ensure that only one material is dispensed at a required time, to avoid any mix-ups.

Able to verify and ensure the housekeeping of the area is in controlled state. Ensure all safety norms are followed in respective area. Keep self and team updated about CGMP requirement. Ensure completion of all required training for self as well as team.

As per the requirement the candidate able to handle the the cleanliness and environmental norms of various area like dispensing, including airlocks and if any deviation is found, document and escalate the point, get it corrected immediately in coordination with production Sub Department Manager and QA Sub Department Manager as per defined Standard Operating Procedure (SOP), and then start the further process.

Required to ensure cleaning and disinfections of floor, ceiling, wall and equipment as per SOP and managing the the availability of clean room garments.

To supervise the behavior of workers in dispensing area. To check the equipment prior to start further dispensing procedure. Keep self and team updated about CGMP requirement.

To have thorough knowledge of SOP of own working area and ensure to practice it. Ensure that the PM, calibration and validation of equipment/system/facility is completed as per approved schedule.


As per the SOP need to record all the activities in the approved formats at the time of observation/activity is performed.

Timely ensure that the appropriate cleaning is done before commencement of further activity, in case of material spillages