Sr Exec, Quality - QC

This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

1.To carry out the sampling of all the materials according to Standard Operating Procedure (SOP).
2.To ensure the status label on the material and transfer such material in the respective area.
3.To ensure that all activities followed in accordance with the SOP.
4.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.
5.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.
6.To prepare reagents and volumetric solution and standardize it.
7.To check and verify standardization and preparation of reagents and volumetric solution.
8.To raise and implement change control or document change request wherever necessary.
9.To perform chemical analysis
10.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.
11.To perform the calibration of analytical instruments.
12.To follow and ensure Good Laboratory Practices (GLP), Good Documentation Practices and Good Manufacturing Practices (GMP) inside Quality Control.
13.To ensure availability the working & impurities standards as per various pharmacopoeias.
14.To assist Supervisor in preparation of SOP and give suggestions to improve system performance.
15.To check, verify and review the calibration of all the analysis instruments whether performed as per the schedule.
16.To check completion of method transfer successfully in coordination with Analytical Development Lab (ADL) Department.

17.To ensure recording of all the data related to the testing online, on day-to-day basis and ensure traceability of the same.
To make entry into LIMS.
18.
To work for lab readiness for audit and ensure compliance in Laboratory.

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

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