Assoc Scientist I Job at Baxter (Bengaluru)

Assoc Scientist I

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Perform biological risk assessments to determine biocompatibility testing required to demonstrate product safety
Document risk assessments in Baxter qualified systems such as Team Center Unified (TCU), Trackwise 8, Electronic Laboratory Notebook (ELN)
Generate protocols and reports for biocompatibility testing
Manage biocompatibility testing at external laboratories within budget and according to project landmarks
Serve as a study monitor for studies placed at external laboratories and review protocols and reports
Summarize biocompatibility testing in technical documents that may be used for regulatory filing
Develop knowledge and understanding of ISO 10993 series of standards for executing biological assays and toxicological risk assessments per ISO 10993-17 for medical devices
Develop knowledge of global compendia (EX: USP, EP, JP etc) supporting container closure systems registered as drugs
Author BEP/BER for regulatory submissions
Have a working knowledge and understanding of Good Laboratory Practice (GLP) / Good Manufacturing Practice (GMP) and related regulations and guidance

Job Responsibility

Perform biological risk assessments to determine biocompatibility testing required to demonstrate product safety
Document risk assessments in Baxter qualified systems such as Team Center Unified (TCU), Trackwise 8, Electronic Laboratory Notebook (ELN)
Generate protocols and reports for biocompatibility testing
Manage biocompatibility testing at external laboratories within budget and according to project landmarks
Serve as a study monitor for studies placed at external laboratories and review protocols and reports
Summarize biocompatibility testing in technical documents that may be used for regulatory filing
Develop knowledge and understanding of ISO 10993 series of standards for executing biological assays and toxicological risk assessments per ISO 10993-17 for medical devices
Develop knowledge of global compendia (EX: USP, EP, JP etc) supporting container closure systems registered as drugs
Author BEP/BER for regulatory submissions
Have a working knowledge and understanding of Good Laboratory Practice (GLP) / Good Manufacturing Practice (GMP) and related regulations and guidance

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Assoc Scientist I-2

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

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

Fulltime

Assoc Scientist I-2

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

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

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

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Assoc Scientist I-1

This is where your work makes a difference. At Baxter, we believe every person—r...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Perform biological risk assessments to determine biocompatibility testing required to demonstrate product safety
Document risk assessments in Baxter qualified systems such as Team Center Unified (TCU), Trackwise 8, Electronic Laboratory Notebook (ELN)
Generate protocols and reports for biocompatibility testing
Manage biocompatibility testing at external laboratories within budget and according to project landmarks
Serve as a study monitor for studies placed at external laboratories and review protocols and reports
Summarize biocompatibility testing in technical documents that may be used for regulatory filing
Develop knowledge and understanding of ISO 10993 series of standards for executing biological assays and toxicological risk assessments per ISO 10993-17 for medical devices
Develop knowledge of global compendia (EX: USP, EP, JP etc) supporting container closure systems registered as drugs
Author BEP/BER for regulatory submissions
Have a working knowledge and understanding of Good Laboratory Practice (GLP) / Good Manufacturing Practice (GMP) and related regulations and guidance

Job Responsibility

Perform biological risk assessments
Document risk assessments in Baxter qualified systems
Generate protocols and reports for biocompatibility testing
Manage biocompatibility testing at external laboratories
Serve as a study monitor
Summarize biocompatibility testing in technical documents
Develop knowledge of ISO 10993 series standards
Develop knowledge of global compendia
Author BEP/BER for regulatory submissions
Work with GLP/GMP regulations

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Assoc Scientist I-2

This is where your work makes a difference. At Baxter, we believe every person—r...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

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

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

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

New

IT Training Lead

The IT Training Lead will drive technology learning and user adoption across the...

Location

United States , Delray Beach

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Experience in IT training, instructional design, technical enablement, or learning and development
Strong knowledge of Microsoft 365
Excellent communication, facilitation, and content development skills
Ability to translate technical concepts into practical, user-friendly training.

Job Responsibility

Design, develop, and deliver IT training programs in instructor-led, virtual, and self-paced formats
Take lead in the Microsoft Copilot and AI training strategy, including onboarding, advanced use cases, responsible AI usage, and ongoing enablement
Partner with IT leadership to support new technology rollouts, system upgrades, and digital transformation initiatives
Create and maintain training content, including videos, guides, tutorials, and job aids
Identify skill gaps and develop targeted learning solutions to improve adoption and productivity
Gather feedback and measure training effectiveness to continuously improve programs.

New

K Kitchen Representative

The position includes, but is not limited to, the following essential job duties...

Location

United States , New Albany

Salary:

Not provided

Circle K

Expiration Date

Until further notice

Requirements

Excellent communication skills
Team player who can work well with others or independently
Acts with integrity
keeps commitments
Contagious positive attitude
Focuses on achieving results while having fun
Frequently bend, twist at waist, kneel, squat, stand, and walk
Occasionally climb and descend ladders
Tolerate extreme cold and hot temperatures and work in and around fryers, ovens, grills, coolers, freezers, sharp objects, and loud noises
Reach, grasp, and manipulate objects with hands for entire shift, including reaching for objects overhead

Job Responsibility

Provides excellent guest service in a fast and friendly manner
Maintains a clean restaurant environment by cleaning and performing general housekeeping duties
Prepares and serves food items in accordance with all Brand, Company, and health department regulations
Ensures product quality, food safety, and operational standards are met
Keeps accurate cash, sales, and inventory control records
Follows all government laws and safety codes
Completes reports on all incidents following our 5-minute rule policy
Lives our Company values: One Team, Do the Right Thing, Takes Ownership, Play to Win

What we offer

Medical, Dental, Vision, Term Life and AD&D plans
Flexible spending and health savings accounts (FT)
Vacation paid time off
Company holidays paid at time and a half
Matching 401(k)
Tuition Reimbursement
Stock Purchase Plan
Employee Discount Program
Discount Meal Benefit
Wellness Plan

New

K Kitchen Representative

Location

United States , Decatur

Salary:

Not provided

Circle K

Expiration Date

Until further notice

Requirements

Excellent communication skills
Team player who can work well with others or independently
Acts with integrity
keeps commitments
Contagious positive attitude
Focuses on achieving results while having fun
Frequently bend, twist at waist, kneel, squat, stand, and walk
Occasionally climb and descend ladders
Tolerate extreme cold and hot temperatures and work in and around fryers, ovens, grills, coolers, freezers, sharp objects, and loud noises
Reach, grasp, and manipulate objects with hands for entire shift, including reaching for objects overhead

Job Responsibility

Provides excellent guest service in a fast and friendly manner
Maintains a clean restaurant environment by cleaning and performing general housekeeping duties
Prepares and serves food items in accordance with all Brand, Company, and health department regulations
Ensures product quality, food safety, and operational standards are met
Keeps accurate cash, sales, and inventory control records
Follows all government laws and safety codes
Completes reports on all incidents following our 5-minute rule policy
Lives our Company values: One Team, Do the Right Thing, Takes Ownership, Play to Win

What we offer

Medical, Dental, Vision, Term Life and AD&D plans
Flexible spending and health savings accounts (FT)
Vacation paid time off
Company holidays paid at time and a half
Matching 401(k)
Tuition Reimbursement
Stock Purchase Plan
Employee Discount Program
Discount Meal Benefit
Wellness Plan

Select Country

Assoc Scientist I

Job Description

Job Responsibility

Requirements

What we offer

Looking for more opportunities?

Assoc Scientist I

Assoc Scientist I

Assoc Scientist I-2

Assoc Scientist I-2

Assoc Scientist I-1

Assoc Scientist I-2

IT Training Lead

K Kitchen Representative

K Kitchen Representative

Our AI answers in your language