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Assoc I, Quality Assurance

Req # JR - 183824 Location Ahmedabad, Gujarat, India Job Category Quality Date posted 11/04/2025
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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 I, Quality Assurance

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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. 

Unique Opportunity

Come join Baxter Healthcare Corporation as a Sr. Executive, Quality Assurance - IPQA, Production in our brand new manufacturing facility in Ahmedabad. This role offers an exciting chance to be at the forefront of ensuring our products meet the highest standards of quality and safety. You will have a key role in upholding our reputation for excellence and be part of a dedicated team committed to making a positive impact.

Key Responsibilities

  • Implement in-process quality assurance activities as delegated by the Supervisor and/or shift lead in each shift.
  • Perform line clearance activities at various stages of packaging as defined in the Batch Packaging record.
  • Perform regular checks during packing process, following batch records, and report any issues to shift lead and supervisor for necessary actions.
  • Ensure challenge tests are performed at defined frequencies for applicable packaging equipment.
  • Collect stability samples, retain samples, and other samples, recording collection details in BPR and ELN.
  • Verify the sample/good destruction process, report any gaps to Shift Lead or Supervisor, and take corrective and preventive actions in coordination with respective functions.
  • Maintain compliance with Good Documentation Practices (GDP) for logbooks, online documents, and records related to our products.
  • Perform Acceptance Quality Limit (AQL) of visually inspected products.
  • Approve pallet planning in the PCR system at the dispatch area.
  • Ensure cGMP compliance during packing and visual inspection processes.
  • Perform, evaluate, and carry out Visual Inspection qualification processes.
  • Prepare and maintain visual inspection qualification kits and records.
  • Carry out stage-wise BPR review for batch execution compliance.
  • Review and verify user access management and audit trails.
  • Perform and support the Continued Process Verification (CPV) program.
  • Ensure the handover of shift-to-shift activities and record in the Shift Charge Handover format/logbook.
  • Perform impact assessments of breakdown maintenance, approve activities in MAXIMO, and review risk assessments.
  • Participate in investigations in case of complaints or non-conformities.
  • Communicate any failures or abnormal notifications to the Supervisor and shift lead for timely issue resolution.
  • Raise Document Change Requests (DCR) and Change Control Management (CCM), supervise them, and ensure closure as per Standard Operating Procedures.
  • Perform any other responsibilities assigned by the shift lead and reporting manager.

Qualifications

  • Validated experience in a quality assurance role within a manufacturing environment.
  • Strong understanding of cGMP and GDP requirements.
  • Outstanding attention to detail and dedication to maintaining high-quality standards.
  • Excellent communication skills and ability to work collaboratively in a team-oriented environment.
  • Ability to closely enforce to protocols and procedures.
  • Proven ability to optimally conduct quality assurance processes and improvements.

Why Baxter?

At Baxter, you will be part of a collaborative and inclusive environment where your contributions are valued. We offer competitive compensation, opportunities for growth, and a chance to be part of a team that is committed to delivering outstanding products. Join us and make a difference in the lives of people around the world.

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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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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