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Assoc Eng, Eng Services - LMC

Req # JR - 148677 Location Ahmedabad, Gujarat, India Job Category Quality Date posted 09/19/2024
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Overview

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.

  • Support for Parents

  • Continuing Education/ Professional Development

  • Employee Heath & Well-Being Benefits

  • Paid Time Off

  • 2 Days a Year to Volunteer

Success Profile

What makes a successful Quality team member at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.

  • Detail Oriented
  • Continuous Learner
  • Courageous
  • Collaborative
  • Critical Thinker
  • Influential

Assoc Eng, Eng Services - LMC

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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 investigate, review and approve any Out of limit (OOL) or Non-conformity Report or Laboratory Incident and take the corrective and preventive actions (CAPA) if required.

To facilitate internal quality audits to ensure the compliance to all systems and procedures.

To ensure that system and facilities comply as per the regulatory requirements and expectations.

To ensure and sustain all time readiness in line with current regulatory expectations for regulatory authorities and other partner inspection.

To ensure process and systems are complying as per standard written procedures.

To ensure compliance against audit observations and ensure effectiveness of Corrective & Preventive Action (CAPA).

To ensure completion of assigned training of Utility Department.

To operate electronic QMS modules for review and approval of changes, procedures for Utility Department.

To ensure that data integrity is being maintained at all levels and to perform regular checks to ensure that system is in state of control.

To ensure that the key responsibilities are well defined, built into the executor level and monitored periodically.

To ensure Department is in line with cGMP compliance as per global regulatory requirements

To prepare and update the error free and user-friendly documents.

To raise Change Control for any changes in approved processes and system. Also execute & close impact analysis and Change Control Tasks in timely manner.

To review & investigate Quality Management System (QMS) elements such as non-conformance (NCR), Corrective & Preventive action (CAPA) for Utility in Track wise.

To attend and implement training related to Quality Management System (QMS) and current Good Manufacturing Practice (cGMP) and ensure the on-time training completion of Utility Team.

To check & verify that data integrity is being maintained at all levels by frequent GEMBAs.

To act as Author and prepare Quality Management System (QMS) related documents such as Standard Operating Procedure (SOP), Exhibit, Standard Format, User requirement specification (URS), Qualification protocol, etc. in TcU and ensure the documents are in line with current Good Manufacturing Practice (cGMP) requirements

To track & comply with Quality Key Performance Indicators (KPIs) metrics & take corrective action to ensure such performance metrics are within the target achievement.

To face an internal or external current Good Manufacturing Practice (cGMP) regulatory audits & respond to the auditors’ queries. Also ensure audit preparedness in the function.

To escalate to Manager if any abnormalities or non-compliance in Utility function

 To assist Manager carrying out Energy saving activity and its monitoring system continuously with every year Energy reduction goal.

To assist Manager in carrying out projects for awareness of safety, improvement in operation efficiency and cost optimization.

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

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

148677
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Address

Explore this location Sarkhej - Bavia Road
Chacharvadi Vasna
Ahmedabad- 382213
Gujarat
India
Explore This Location

Hear from Our Employees

Our company is enriched by a diverse population of individuals in more than 100 countries that work to solve, innovate, manufacture and drive better healthcare options for patients around the world.

Meet Christelle, Senior Quality Manager in Malta

“I was an Engineering Graduate with a Master's in Business Administration, and was more inclined toward working with people than with machines. When I came across an opportunity to work with Baxter as a Quality Engineer, it was the perfect combination: a manufacturing environment and a role that required me to collaborate with multiple teams daily. Baxter's mission of saving and sustaining lives gives me all the purpose and fulfilment I need.”

Meet Lorena, Senior QA Associate in London, UK

“I am registered pharmacist in the UK with experience with drug products and final product release. I am very dedicated to my work and accurate in details to ensure correct assessment is provided to our customers to ensure patients' safety.”

Meet Gary, Quality Research Manager in Singapore

“I have always enjoyed working at Baxter and I find here to be a great place to work! Management truly cares for you, and invests time and resources to support your career goals and aspirations. My current role provides me the opportunity to work with culturally diverse teams, bringing different talents together, learning from one another and working toward a common goal and mission.”

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