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Assoc Scientist I-2

https://www.baxter.com/ Logo

Baxter

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Location:
India , Bengaluru

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Contract Type:
Not provided

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Salary:

Not provided

Job Description:

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.

Job Responsibility:

  • Serve as a verifier of biocompatibility information documented in protocols, reports, toxicology risk assessments, BEP/BER or materials in the material database
  • Maintain the Material Database in Team Center Unified (TcU) and serve as the system administrator Validating software updates made to the material database
  • Generation of purchase orders for work performed at the external laboratories
  • Employ appropriate techniques/methods to execute routine assignments successfully and independently within negotiated deadlines
  • Maintain knowledge of relevant regulatory and biocompatibility requirements in accordance with ISO 10993 series of standards for device registration and global compendia for drug registrations
  • Recommend appropriate designs, techniques, and processes for a specified sequence of tasks where needed
  • Have a working knowledge and understanding of Good Laboratory Practice (GLP) / Good Manufacturing Practice (GMP) and related regulations and guidance
  • Receiving and handling samples for testing, coordinating sample shipments to external laboratories

Requirements:

  • Serve as a verifier of biocompatibility information documented in protocols, reports, toxicology risk assessments, BEP/BER or materials in the material database
  • Maintain the Material Database in Team Center Unified (TcU) and serve as the system administrator Validating software updates made to the material database
  • Generation of purchase orders for work performed at the external laboratories
  • Employ appropriate techniques/methods to execute routine assignments successfully and independently within negotiated deadlines
  • Maintain knowledge of relevant regulatory and biocompatibility requirements in accordance with ISO 10993 series of standards for device registration and global compendia for drug registrations
  • Recommend appropriate designs, techniques, and processes for a specified sequence of tasks where needed
  • Have a working knowledge and understanding of Good Laboratory Practice (GLP) / Good Manufacturing Practice (GMP) and related regulations and guidance
  • Receiving and handling samples for testing, coordinating sample shipments to external laboratories
What we offer:
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer

Additional Information:

Job Posted:
May 04, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

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