Sr Exec I, Quality Control

This is whereyour work makes a difference.

At Baxter we believe every personregardless of who they are or where they are fromdeserves 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 jobyou 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) Good 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 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.

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