Research Associate Iii Job in Baxter

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We believe every person deserves a chance for a healthy life, free from illness and full of possibility. We see a world full of healing, with viable care options available to those with limited choices today. We envision new ways of providing physicians, pharmacists and nurses with technologies that not only treat chronic diseases, but also work to prevent them. Were looking for team members who are motivated to learn, grow and innovate, while making a meaningful difference for millions of people around the world.

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Job Summary

Scientist with expertise in toxicology and product safety evaluation including development of nonclinical plans for drug development, toxicology and impurity study design development and monitoring, and development of toxicology risk assessments. Hazard evaluation of chemicals used in manufacturing. In-depth knowledge in Toxicology or a related field required.

Essential Duties and Responsibilities

Generation of toxicology risk assessment in accordance with ICH and ISO10993-17. Hazard evaluation of chemical and pesticide used in manufacturing Maintain current knowledge of relevant regulatory requirements related to toxicology, product development, design and safety. Perform as preclinical/toxicology representative on project teams Utilize Lhasa Derek and Sarah Nexus software to assess toxicological endpoints. Independently plan and execute a series of design and/or technical tasks that may not be well-defined, have multiple variables, and require advanced techniques within negotiated deadlines. Devise 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

Qualifications

The position requires relevant technical knowledge in toxicology and safety evaluation. General understanding of pharmacology highly desired. Ability to understand and apply global regulatory guidelines including OECD and FDA GLP, ICH guidance, ISO10993. Good oral and written communication in English language. Utilize a logical, methodical approach when problem solving, developing solutions and making recommendations. Ability to work independently and prioritize assignments to meet project schedules. Ability to make routine decisions independently.

Ability to design experiments, monitor toxicology studies, interpret the results and draw meaningful conclusions from the data

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, 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 protected] and let us know the nature of your request along with your contact information.