Baxter Recruitment Drive; Hiring Associate Quality Control – Apply Now

This is where you make a difference in our patients’ safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people’s lives. Candidates are advised to apply soon, before the link expires

Name of the Organization: Baxter

Requisition ID: JR - 151949

Positions: Assoc, Quality Control - QMS

Location: Ahmedabad

Salary: As per company Norms

Educational Qualifications:

• Graduate

Job Description:

At Baxter, they are deeply connected by their 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 they know their 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, they have pioneered significant medical innovations that transform healthcare. Together, they create a place where they are happy, successful and inspire each other. This is where you can do your best work. Join them at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

• To review, update, report and inform Supervisor as & when deviation is initiated.
• To ensure that the recording of NCR is done in line with standard operating procedure
• To ensure the implementation of GMP, GDP practices and review of issues and impact of the same, if any, & take corrective actions.
• To carry out GLP rounds in the Quality Control lab.
• To work as a Good Manufacturing Practice (GMP) inspector in the plant
• To train/update the team members on various regulatory guidelines
• To identify, monitor the deviation/abnormalities in process/documents/systems are captured and resolve them according to Quality management System.
• To ensure that all the deviations and OOS are reported to QA within required time frame.
• To prepare, review, Implement and update SOP’s according to current regulations systems.
• To conduct Technical committee meeting on CCN impact assessment.
• To conduct monthly corrective and Preventive Action Meeting.
• To review the CAPA summary report and ensure that all CAPA are closed within time frame.
• To review Change Control Note and NCR report before sending to Quality Committee for final closure and ensure the timely closure of Change Control Note and NCR
• To train/update the personnel for the various aspect of current Good Manufacturing Practices.
• To investigate and close the QMS elements in timely manner.

 

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