Openings in Baxter for Research Associate-I in Analytical, QA batch release and Engineering project Leader

Openings in Baxter for Research Associate-I in Analytical, QA batch release and Engineering project Leader

   


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 : 

Masters with a minimum of 2+ years in relevant science discipline (Analytical/ Pharma/ Pharmaceutical analysis) 

Qualification : 

Required to have experience in LC-MS/ MS, GC-MS and ICP-OES/ ICP-MS 

Experience with analytical tools and instruments and wet chemistry lab for the sample preparation 

Need to have experience with written and verbal communication skills in English.

Required to demonstrate the ability to resolve the technical challenges

Able to work properly with the cross functional teams and and adapt to the changes and have the agile mindset.

Required to adapt the changes in diversity, inclusion and value difference.

Able to apply the technical theory and principle and project with in the area of expertise 

Required to work with the quality standard and document the lab work and perform the Baxter GDP 

Need to follow the Baxter quality SOP and manual with Health, safety and EHS guidelines, able to work independently and enhance the lab capability and productivity.

For QA Batch Release 


Required to comply with the cGMP and able to handle the change control and prepare the batch rejections and handle the pre defined specifications and handle the non confirmances 

Required to prepare, review the SOP and change management reports 

Handling the Batch release data for the compliance and ensure the closure of CAPA and submit the batch documents ti IRA as per the requirement