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Location
In office (Bengaluru)
Seniority
Middle · 3+ years exp
Visa
Sponsors visas in United Kingdom; no register of this country names it
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 11, 2026. First seen by Alion on Nov 11, 2026. Baxter scores A on the Alion truth index.

Overview
Company
Impact
Profile match
Baxter International is a global medical technology company headquartered in Deerfield, Illinois, producing infusion systems and pumps, injectable medicines, surgical products, hospital beds and patient mobility, care communications and diagnostic equipment. Founded in 1931 and listed on the New York Stock Exchange, it serves hospitals, physician offices and other care settings worldwide, with manufacturing and R&D sites in the US, Puerto Rico, Costa Rica, Europe and India. It hires sales and clinical account managers, regulatory affairs, quality and R&D engineers, field service technicians, manufacturing operators and finance and IT staff.
Backed by Warburg Pincus

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.

Your Role at Baxter

Support the Sustaining Engineering team in maintaining and improving existing products, processes, and systems. Participate in the Site/Product Operations or Single Point Ownership (SPO) team, focusing on Change Management activities. Coordinate and track engineering changes, product updates, and process modifications through established quality and regulatory procedures.

What You’ll Be Doing

  • To ensure successful initiation, planning and completion of small or complex project through monitoring, tracking and analyzing project activities and metrics.
  • Serve as SPOC for team and collaborate with project stakeholders.
  • Handling of Change controls/Change Management activities.
  • Ensure implementation of quality processes including change control and design control activities.
  • Preparation and review of project related documents, protocols and reports as required.
  • Assist Project Manager in reviews and ensure project complies with QA processes and adhering to defined timelines.
  • Review changes to existing process and products and drive them via change control and ensure timely completion/closure.
  • Work with global team, co-ordinate with different stakeholders (PDO, QA, RA, etc) to understand their requirements, prioritize the tasks & ensure completion.
  • Participate as well as lead the meetings with cross functional team to communicate priorities, requirements, key issues/risks and ensure they are completely understood and set clear expectations.
  • Independently drive the change controls.
  • Resolve queries, concerns (as needed) & drive the project to completion.

What You’ll Bring

  • Bachelor’s or Master’s degree in Bio Medical /Mechanical Engineering or Equivalent with 3+ years of experience in Sustaining Engineering projects.
  • Excellent verbal and written skills in english.
  • Excellent communication and presentation skill. Should be able to communicate effectively in a multi-cultural working environment.
  • Strong collaboration and interpersonal skills.
  • Ability to co-ordinate with stakeholders of cross functional and Leadership Team.
  • Excellent critical thinking and problem-solving skills and application of methods and tools.
  • Independent worker as well as Team Player with strong execution abilities to complete projects within timeline.
  • Knowledge of (U.S.) & EU Regulations and medical device standards - ISO 13485, ISO 14971.
  • Good to have experience in Change Management process and tools.

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

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.

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