Associate I, Lab QA

This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride. 

QUALITY:

• To review the Raw material, packing material and finished product specification and to update department Head whenever required.

  
  
  

•  To carryout investigation in case of out of specification (OOS) and deviation and take the corrective and preventive action (CAPA).

  
  
  

• To ensure the calibration of all the analysis instruments is accurate.

  
  
  

• To sign off electronically the final document of sample set generated through Empower and all other softwares where (E-signature is applicable) for all the analysis in QC, stability & microbiology.

  
  
  

• To ensure the preparation of working standards as per the guidelines and pharmacopoeias.

  
  
  

• To ensure the review of calculation of the respective test protocol and daily release status.

  
  
  

• To ensure the testing of Raw material and packing material and analysis of in-process and finished product sample and it’s release according to standard operating procedure and specification.

  
  
  

• To ensure recording and documentation of all the data related to the testing on-line on daily basis and ensure the tractability of the same.

  
  
  

• To ensure preparation of the reagent and volumetric solutions.

  
  
  

• To support team members in preparation of SOPs.

  
  
  

• To review calibration reports.

  
  
  

• To escalate any abnormal results to department Head.

  
  
  

• To sign all the necessary test records and review the results of all the testing.

  
  
  

• To review real time analysis data as and when required.

  
  
  

• To review audit trails of analytical instruments as per defined procedure.

  
  
  

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Administrative:

• To initiate and attend the quality related meetings and work towards quality culture.

  
  
  

• In absence of executive, Department Head will ensure these roles & Responsibilities.

  
  
  

• In absence of Department Head, Divisional Head will ensure these roles & Responsibilities.

  
  
  

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice
Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.