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.
- To ensure the implementation and maintenance of Current Good Manufacturing Practice
- (cGMP) standards and all To enumerate and report the tubes and plates and to supervise the discarding method of the same.
- To perform periodic microbiological tests, as per Standard Operating Procedure (SOP). To perform the Bacterial Endotoxin Test.
- To test the material for their pre-sterile bio-burden and to test Raw Material (RM)/ Packing Material (PM) for bio-burden test.
- To co-ordinate with Technical department for any kind of machine related abnormality, which might be affecting the quality of the product, and its microbiological content.
- To take the samples for sterility test and to carry out the sterility testing.
- Document contemporaneously all the activities performed.
- To test water samples for physicochemical tests, Biochemical and chemical tests and to document the activities.
- To maintain and update stock record of Limulus Amoebocyte Lysate (LAL) reagents. To qualify the personnel to enter in to the clean.
- To keep track of requirement for procurement and give monthly requirement to executive. To qualify the prepared media for growth promotion test.
- To perform gram staining of daily-observed colonies and identify them on BBL crystal. To perform the microbiological analysis of stability sample as per daily plan of work & in line with standard operating procedure.
- To perform the method validations as per the laid down protocol and to support qualification activities to support validation /qualifications.
- To prepare, maintain and reconcile Standard and house isolates / cultures for routine use. To maintain and update media stock record formats and in state of compliance.
- To intimate executive for any abnormalities in microbiological analysis. However, in the absence of executive, intimate the status of the same to Department Head.
- To support OOS, QMS, and other QMS elements towards timely closure.
- To perform the assigned activities other than or in addition to routine activities by supervisor, HOD or management team as and when organization needs.
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.
