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Sr. Executive, Quality Control - RMPM

Req # JR - 146380 Location Ahmedabad, Gujarat, India Job Category Quality Date posted 09/26/2024
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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

Sr. Executive, Quality Control - RMPM

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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 carry out the sampling of all the materials according to Standard Operating Procedure (SOP).
  • To carry out the testing of Raw Material and Packing Material according to approved standard test procedure.
  • To support Sub-Department Manager in releasing of Raw Material and Packing Material
  • To carry out the calibration of instruments as per the schedule.
  • To coordinate with stability department for the working standards as per the guidelines and various pharmacopoeias.
  • To ensure the status label on the material and transfer such material in the respective area.
  • To prepare reagent & volumetric solution and standardize it.
  • To carry out all the necessary tests as per respective specification and procedure and record the results for all the materials.
  • To check the stores and ensure the implementation of GMP norms in the stores.
  • To inform to superior immediately in case of any Out of Specification result or Non-conformity or Laboratory Incident observed or any instrument breakdown.
  • To review the sampling activity of all the materials performed by team members.
  • To assess the results of testing of Raw Material, Packing Material products to ensure alignment with standard operating procedure (SOP) and regulatory guidelines.
  • To review results of the tests against the specification & Standard Test Procedure performed by team members.
  • To ensure availability of the working & impurities standards as per various pharmacopoeias.
  • To ensure the status label on the material and transfer such material in the respective area.
  • To support Sub-Department Manager, in investigation of out of specification (OOS), non-conformity and Laboratory Incident Report (LIR) and take corrective and preventive actions.
  • To check and verify standardization and preparation of reagents and volumetric solution.
  • To review periodic observation of retained sample done by team members
  • To follow and ensure Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP) and Good Documentation Practices inside QC.
  • To support & guide team members in implementing change control, Corrective and preventive actions (CAPA) and check effectiveness of CAPA, give suggestions form Divisional Head if required.
  • To train team members on current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP) and Good Documentation Practices.
  • To assist Sub-Department Manager in formation of SOP and give suggestions to improve system performance.
  • To check, verify and review the calibration of all the analysis instruments whether performed as per the schedule.
  • To ensure recording of all the data related to the testing online, on day-to-day basis and ensure traceability of the same.
  • To check completion of method transfer successfully in coordination with Analytical Development Lab (ADL) Department.

Preferred Educational Qualification:

  • M Sc / M Pharm / B Pharm
  • Candidate must have 3 - 6 yrs. of working experience in QC department (i.e. pharma industry)

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.

146380
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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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