Associate, Micro

2 weeks ago

Ahmedabad Gujarat, India BAXTER Full time

**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 ensure closure of control form system of microbiology team by tracking the open CFS forms
- To ensure the completeness of training of microbiology team by tracking the ongoing trainings through BaxU.
- To be responsible for the closure of training request form and completeness of training before SOP effective
- To ensure and update curriculum whenever there is any updation in SOP.
- To ensure the timely archival of document in QA doc cell through Baxcabinet.
- To ensure calibration and validation of instruments in microbiological laboratory through calibration schedules in coordination with Quality Assurance function.
- Participate in GEMBA rounds and supervises system and facilities are complying with GDP and GLP as per the requirements and train employees on such requirements as necessary and sustain GMP compliance in the lab.
- Maintain availability of all the stock always used in Microbiology lab through tracking mechanism and giving requirements to procurement team through weekly/monthly/annual basis.
- Maintain the destruction logbook for the destruction of document of microbiology.
- Perform periodic gap & risk assessment of procedure vs practices and propose alternate method/escalate to the Manager.
- Track the destruction of documents, scrap and bio waste by maintain logbooks.
- Escalate machine related abnormality to the technical department by initiating, tracking and closure of service log through the tool.
- To perform the new instruments /Equipment’s Qualification so as to meet the given standards.
- To perform the review of Laboratory Logbooks and ELN to ensure the correctness of documents.
- To ensure the clean environment for sterile preparation by implementing the Good Manufacturing Practice (GMP) norms as per the international standards and guidelines.
- To do sampling of Water for Injection (WFI), double Reverse Osmosis (DRO), Single Reverse Osmosis (SRO), raw water and pure steam.
- To collect the validation samples as per validation protocol
- To prepare trends of the results obtained
- To qualify the personnel to enter in to the clean room.
- To perform HEPA filter qualification on periodic basis and as and when required
- To operate laboratory instrument or equipment as and when required.
- To initiate non-conformity or Out of Specification in case of abnormality observed.
- To perform data entry for trend analysis of the daily result observed.
- To communicate any failure or abnormal notification to respective Supervisor for their attention and to seek the solution.
- To bring to the notice of Supervisor about the abnormalities in the clean room or manufacturing areas and suggest the preventive and corrective measures in case of such abnormalities as per the guideline.

Bachelor's Degree (±16 years) - Microbiology, Master's Degree (±18 years) - Microbiology

**Reasonable Accommodations**

**Recruitment Fraud Notice**

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132095

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