Job type full-time
Full job description
This is where you save and sustain lives
At baxter, we are deeply connected by our missionNo matter your role at baxter, your work makes a positive impact on people around the worldYou`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 homeFor 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 otherThis is where you can do your best work.
Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.
Toxicologist – research associate ii, pre-clinical
Scientist with knowledge in toxicology and product safety evaluation including development of nonclinical plans for drug
Development, development of toxicology risk assessments, designing toxicology studies & monitoringHazard evaluation
Of chemicals used in manufacturingIn-depth knowledge in toxicology.
Essential duties and responsibilities
1Generation of toxicology risk assessment in accordance with ich and iso10993-17 independently or under
2Hazard evaluation of chemical and pesticide used in manufacturing
3Maintain current knowledge of relevant regulatory requirements related to toxicology, product development, design
4Perform as preclinical/toxicology representative on project teams
5Utilize lhasa derek and sarah nexus software to assess toxicological endpoints.
6Under supervision or independently plan and execute a series of design and/or technical tasks that may not be welldefined,
Have multiple variables, and require advanced techniques within negotiated deadlines.
7Devise new approaches to complex problems through adaptations and modifications of standard technical principles.
Incorporate new methods and technologies for improving existing or new products/processes
8Assist in or independently develop toxicology risk assessments using innovative solutions to address safety through
The use of multiple disciplines and technical principles.
9Independently review literature and identify relevant articles to support product development and registration.
10Incorporate advanced theories, methods and technologies from around the world to develop new innovative
11In addition to having an in-depth knowledge and understanding of gxp and related regulations and guidance, is able
To provide expert insights into such regulations so as to facilitate efficient product registration and/or is an active
Participant in the generation, review, adoption and interpretation of such regulations.
12Utilize siemens teamcenter unified global material management system (gmms) for biocompatibility testing and
Product development and registration support.
13Assist in developing project schedules; provide estimates and timelines to meet project milestones.
14Perform regulatory toxicology assessments in trackwise 8 and work with cross functional team members in order to
Determine a comprehensive testing strategy
1The position requires relevant technical knowledge in toxicology and safety evaluationGeneral understanding of
Pharmacology highly desired.
2Ability to understand and apply global regulatory guidelines including oecd and fda glp, ich guidance, iso10993.
3Good oral and written communication in english language.
4Utilize a logical, methodical approach when problem solving, developing solutions and making recommendations.
5Ability to work independently and prioritize assignments to meet project schedules.
6Ability to make routine decisions independently.
7Ability to design experiments, monitor toxicology studies, interpret the results and draw meaningful conclusions from
Education and experience:
Master of veterinary science/ pharmacology/life-sciences with 7-10 years of work experience of in vivo and/or vitro pre-
Clinical toxicological evaluations and risk assessmentCandidate with dabt certification will be preferred.
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilitiesIf, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to email@example.com and let us know the nature of your request along with your contact information.
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Posted 30+ days ago