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 carry out the sampling of all the materials according to Standard Operating Procedure SOP To ensure the status label on the material and transfer such material in the respective area To ensure that all activities followed in accordance with the SOP To perform the analysis as per the specification standard test procedure and record the necessary results in respective documents for Raw Material Packing material In-process sample Validation sample finish products and other samples To involved and support in investigation of failure of any material or product in case of any out of specification OOS or OOT or laboratory incident or non-conformity and take corrective and preventive actions To prepare reagents and volumetric solution and standardize it To check and verify standardization and preparation of reagents and volumetric solution To raise and implement change control or document change request wherever necessary To perform chemical analysis To assess the results of testing of Raw Material Packing material In-process sample Validation sample finish products and other sample to ensure alignment with standard operating procedure SOP and regulatory guidelines To perform the calibration of analytical instruments To follow and ensure Good Laboratory Practices GLP Valuable Documentation Practices and Good Manufacturing Practices GMP inside Quality Control To ensure availability the working impurities standards as per various pharmacopoeias To assist Supervisor in preparation of SOP and give suggestions to improve system performance To check verify and review the calibration of all the analysis instruments whether performed as per the schedule To check completion of method transfer successfully in coordination with Analytical Development Lab ADL Department To make entry into LIMS To ensure recording of all the data related to the testing online on day-to-day basis and ensure traceability of the same To work for lab readiness for audit and ensure compliance in Laboratory Equal Employment Opportunity Baxter is an equal chance 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

📌 Sr Exec I, Quality Control (Gujarat)
🏢 BAXTER
📍 Gujarat