Sr. Quality Engineer

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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

Sr. Quality Engineer

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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.

To review executed protocols of equipment, utility, process validation, cleaning validation, Utility and facility /HVAC qualification.
To coordinate with cross functional departments for execution of all validation activities & escalate to HOD regarding any non-conformity from planning.
To review calendars for various periodic qualifications & get it reviewed and approved by HOD.
To track QMS documents like Change Control Management, Corrective and Preventive Action, OOS and Non-conformance for the validation activity and review and approve the investigation report.
To ensure timely closure of the DCRs, CCM tasks, investigation report due to any NCR/OOS.
To ensure timely completion of the self and subordinated assigned trainings.
To participate in the Change Control Pre- Assessment meetings and perform the impact assessment of the assigned change controls in Trackwise.
To review and approve the scheduled validation activity as per monthly calendar and send it to the cross functional & Planning department in advance for execution planning before the scheduled date.
To ensure implementation of validation, qualification activities & inform HOD for any non-conformity deviated from written procedure.
To ensure timely/contemporaneous (wherever applicable) data recording and compilation of reports during execution.
To co-ordinate with projects and other cross functional departments. for prior information on new equipment installation and review respective protocol in TcU followed by qualification of new equipment and get it approved by HOD.
To review summary report for submission to International Regulatory Affairs (IRA) as a part of queries or ANDA submission.
To guide and coach team for protocol creation, planning & execution & preparation of validation report.
To ensure compliance with validation/qualification requirements as per regulatory requirements and to update the documents to meet the expectations.
To ensure SOPs/ Protocols are in-line with regulatory and Baxter Global Requirements (GQRs) and Procedure (GQPs).
To update, review and approve Validation Master Plan in compliance to regulatory requirement and site validation policy.
To escalate the activity or issues which might occur during second and night shift validation activities to HOD.
To escalate any potential challenges for execution of any validation /qualification activities.
To participate during any internal or external inspection and prepare the audit response.
To prepare shift schedule as per the validation activity and ensure business needs are fulfilled on time.
To be vigilant of safety aspects and record hazard or any near miss in the provided portal. To assist the department, lead for the preparation of the budget and ensure the expenses as per allocated budget.
To intimate Production & Production Planning and Availability (PPA) department in advance for process validation & qualification activities.
To review and approve documents related to Validation activities and other documents related to Operation.

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
Gujarāt
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.”

Join Our Talent Community

We're grateful for your interest in a career with Baxter, and would like to get to know you. Joining our Talent Community is a great way to stay connected, learn more about Baxter, and help our recruiters find you if there's an opportunity that aligns with your background, skills and interests.

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Sr. Quality Engineer

Overview

Success Profile

Sr. Quality Engineer

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Hear from Our Employees

Meet Christelle, Senior Quality Manager in Malta

Meet Lorena, Senior QA Associate in London, UK

Meet Gary, Quality Research Manager in Singapore

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Join Our Talent Community