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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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Category:
Research and Development

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Contract Type:
Not provided

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Salary:

Not provided
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Job Description:

This is where new knowledge is discovered. Baxter’s Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients needs globally. From Scientists to Engineers, your work creates the products that save and sustain lives.

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
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