Microbiology Specialist Position at Baxter – Apply Now!
Supr, Microbiology
Req # JR – 140623
Location: Ahmedabad, Gujarat, India
Job Category: Microbiology
Date posted: 06/26/2024
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.
- To review the Master protocols and take approval of superior.
- To review the Standard Operating Procedure (SOP) according to the current regulatory requirements and forward to Department Head for final approval.
- To ensure the clean environment for sterile preparation by implementing the Good Manufacturing Practice (GMP) norms as per the international standards and guidelines.
- To review the yearly calendar such as calibration and Performance Qualification (PQ) Calendars.
- To ensure calibration and validation of instruments in microbiological laboratory.
- To review and approve reports of microbiological validations.
- To establish test protocol designs for scientific validation of test methods, equipment and instruments used in testing or monitoring aspects of product quality.
- To ensure that BET, Bioburden and Sterility test are conducted as per the schedule.
- To ensure other periodic microbiological tests as per Standard Operating Procedure (SOP).
- To capture the abnormalities in the process, system or documents and resolve them according to Quality management system.
- To carry out investigation in case of Out of specifications (OOS) and take the corrective and preventive actions (CAPA).
- To suggest effective Corrective and Preventive Action (CAPA) for the abnormalities observed and ensure its implementation.
- To keep track of regulatory commitments and ensure fulfilment of the same.
- To periodically conduct the training programmes for the personnel working in the clean room to ensure the effectiveness of the same on Good Manufacturing practices, Good Laboratory Practices, health, hygiene and maintenance of clean room environment by following the right procedure.
- To look after the administration of personnel to ensure that they are adequately supported, trained, developed and adhere to the quality standards.
To view the original job posting and apply, click here.
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