Associate, Microbiology

3 - 10 years

5 - 12 Lacs

Posted:5 hours ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

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 prepare Standard Operating Procedure (SOP)/documents/Investigation for Microbiology lab and report to Supervisor and Quality Assurance (QA), if the non-conformity is observed.
  • To initiate the change in process, equipment or facility as per operational requirement.
  • Timely closure of CAPA/NCR/LIR and quality documents related to Microbiology lab.
  • To access the impact of functional and cross functional document change control (DCR) or change control management (CCM).
  • To perform investigation non-conformity identified.
  • To initiate CCM and impact assessment of the cross functions through QMS.
  • To prepare error free document as per Corrective and Preventive Action.
  • To impart the training to concerned personnel as per requirement.
  • To handle QMS documents and relative documentation to its closure in defined timeline.
  • To prepare SOP and update according to cGMP requirements or any observation.
  • To perform the task, which assigned by the management from time to time.
  • To prepare and analyze the non-conformity or Out of Specification line wise.
  • To ensure cGMP violation escalation to the Supervisor for their attention and to seek the solution.
  • To escalate any non-compliance observed on shop floor to Supervisor.
  • To intimate and discuss the non-conformity report and its impact with Supervisor and implement appropriate CAPA.
  • Prepare SOP, protocols, standard testing, specification as per the regulatory guidelines
  • Coordinate with QA/QC/QMS/Audit & Compliance personnel for implementation of the current / revised standard testing procedures, specifications and method of analysis.
  • To handle external & internal audits and ensuring effective implementation of CAPA.

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Baxter

Healthcare, Medical Devices

Deerfield

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