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Lab Chemist

Req # JR - 144296 Location Rayong, Rayong, Thailand Job Category Chemistry Date posted 08/06/2024
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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

Lab Chemist

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Vantive: A New Company Built On Our Legacy

Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.

At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us are driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support.

*Completion of the proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions.

Position: Lab Chemist or Analytical Chemist

Location: Nikom Amata City Rayong

Report to: Assistant Manager, Laboratory
Job Scope: Conduct specific chemical and physical analyses on pharmaceutical products through all stages of the manufacturing process from incoming raw materials to finished goods and Stability study, include environmental monitoring programs.

Job Descriptions:

  • Conduct critical chemical and physical analyses such as raw materials, initial, in-process, final products, stability study and samples collected from environmental monitoring programs at Baxter manufacturing facilities, etc.

  • Conduct the incoming inspection (visual, dimensional and functional), review the result and release as per timeline

  • Use a variety of laboratory instrumentation and computer systems to collect and record data (such as LIMS system).

  • Perform assays requiring precise analytical skills and understanding of chemistry principles.

  • Complete all testing, including special project / protocol testing in a timely and appropriate manner.

  • To review the testing result of API, in process, finished product and Stability including result of incoming inspection.

  • Maintain data integrity and ensure compliance with company SOPs and USP specifications, FDA, GLP and cGMP regulations.

  • Ensure that the test results generated within the Chemistry lab are precise, accurate and completed on time.

  • Be responsible for writing validation/Qualification protocols, reports and relevant test methods, new equipment and SOPs.

  • Ensure that the test equipment is calibrated and in good condition before use.

  • Keep tidiness in laboratory and ensure that the laboratory is properly and safely equipped to the international standard.

  • Perform laboratory and manufacturing audits as required. Audit and update, as required, plant SOPs.

  • May perform equipment maintenance and calibrations as required.

  • To review the final analysis result of raw materials, finished product, stability result and document which related within chemical Laboratory.

  • Handling of Supplier Corrective Action Request (SCAR) and INTRA COMPANY CORRECTION/CORRECTIVE ACTION REPORT (ICAR) for packaging material and API.

Qualifications:

  • Bachelor's degree in chemistry, or related science

  • 3 years’ experiences in Quality Control, Analytical Laboratory in a pharmaceutical manufacturing environment

  • Having knowledge in method validation, GMP, PIC/S, ISO 9001, ISO13485, Good Laboratory Practices, and ISO 17025 will be an advantage.

  • Workable command of English and Computer literacy

  • Flexibility in working hours

  • Ability to handle multiple tasks concurrently, and in a timely fashion.

  • Computer literate. Must be detail oriented, conscientious and have high reading comprehension skills.

  • Knowledge of cGMP manufacturing, basic laboratory and pharmaceutical production equipment including but not limited to autoclaves, process tanks, incubators, analytical equipment.

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.

144296
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Address

Explore this location Amata City Industrial Estate 7/398 Moo 6, T. Mapyangporn, A. Pluak Daeng
Rayong
Rayong 21140
Thailand 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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