Allergan
Senior Scientist, Toxicology I
Allergan, Buffalo, New York, United States, 14266
Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at
www.abbvie.com . Follow @abbvie on
Twitter ,
Facebook ,
Instagram ,
YouTube
and
LinkedIn .Job Description
Senior Scientist I, Occupational & Environmental ToxicologistGenetic, Environmental, and Occupational Toxicology (GEO Tox) is a diverse team of scientists with the goals of supporting patient, environmental, and employee safety. The candidate will complete risk assessments supporting occupational, environmental, and manufacturing functions. The position will support programs across AbbVie’s therapeutic areas and involve a broad range of modalities across all stages from early discovery throughout development to marketed products.We are seeking an experienced risk assessment toxicologist to join our team in Development Sciences, Pre-clinical Safety.Responsibilities
Critically evaluate literature and toxicology reports/summaries and utilize tools such as read-across and in silico data to generate toxicology product risk assessments. This includes toxicology support for extractables and leachables, health-based exposure limits (HBELs) including permitted daily exposure limits (PDEs) and occupational exposure limits (OELs), and environmental risk assessments (ERA), and other contaminants.Successful collaboration with multi-functional teams to align on safety banding for implementation throughout the company.Support occupational health (hazard) categorizations and chemical registrations, i.e., GHS, CLP, and Safety Data Sheet (SDS).Plan and oversee studies for environmental assessments or worker safety studies to support regulatory filings or EHS.Qualifications
Requirements :PhD in toxicology or related discipline, or masters with 5+ years of relevant experience, or bachelors with 8+ years of relevant experiencePrevious experience in a pharmaceutical or industry setting providing risk assessments preferredProven record of successfully evaluating safety risksExcellent collaboration, multi-tasking, and communication skillsExcellent writing skills and attention to detail with workAbility to work in a fast-paced environment and meet project deadlinesDesired skills:Occupational Exposure Banding, Performance-based exposure control limits, or evaluating toxicity data for Safety Data Sheets.Risk assessment authoringKnowledge and implementation with regulatory guidance, i.e., ISO-10993-X, ICHQ3C, ICHQ3D, ICHQ3E.Toxicity data mining in databases and both internal and external literatureBroad range of software proficiency as well as in silico predictive tools for toxicityAdditional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.This job is eligible to participate in our short-term incentive programs.Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.US & Puerto Rico only - to learn more, visit
https://www.abbvie.com/join-us/equal-employment-opportunity-employer.htmlUS & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:https://www.abbvie.com/join-us/reasonable-accommodations.html
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AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at
www.abbvie.com . Follow @abbvie on
Twitter ,
Facebook ,
Instagram ,
YouTube
and
LinkedIn .Job Description
Senior Scientist I, Occupational & Environmental ToxicologistGenetic, Environmental, and Occupational Toxicology (GEO Tox) is a diverse team of scientists with the goals of supporting patient, environmental, and employee safety. The candidate will complete risk assessments supporting occupational, environmental, and manufacturing functions. The position will support programs across AbbVie’s therapeutic areas and involve a broad range of modalities across all stages from early discovery throughout development to marketed products.We are seeking an experienced risk assessment toxicologist to join our team in Development Sciences, Pre-clinical Safety.Responsibilities
Critically evaluate literature and toxicology reports/summaries and utilize tools such as read-across and in silico data to generate toxicology product risk assessments. This includes toxicology support for extractables and leachables, health-based exposure limits (HBELs) including permitted daily exposure limits (PDEs) and occupational exposure limits (OELs), and environmental risk assessments (ERA), and other contaminants.Successful collaboration with multi-functional teams to align on safety banding for implementation throughout the company.Support occupational health (hazard) categorizations and chemical registrations, i.e., GHS, CLP, and Safety Data Sheet (SDS).Plan and oversee studies for environmental assessments or worker safety studies to support regulatory filings or EHS.Qualifications
Requirements :PhD in toxicology or related discipline, or masters with 5+ years of relevant experience, or bachelors with 8+ years of relevant experiencePrevious experience in a pharmaceutical or industry setting providing risk assessments preferredProven record of successfully evaluating safety risksExcellent collaboration, multi-tasking, and communication skillsExcellent writing skills and attention to detail with workAbility to work in a fast-paced environment and meet project deadlinesDesired skills:Occupational Exposure Banding, Performance-based exposure control limits, or evaluating toxicity data for Safety Data Sheets.Risk assessment authoringKnowledge and implementation with regulatory guidance, i.e., ISO-10993-X, ICHQ3C, ICHQ3D, ICHQ3E.Toxicity data mining in databases and both internal and external literatureBroad range of software proficiency as well as in silico predictive tools for toxicityAdditional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.This job is eligible to participate in our short-term incentive programs.Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.US & Puerto Rico only - to learn more, visit
https://www.abbvie.com/join-us/equal-employment-opportunity-employer.htmlUS & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:https://www.abbvie.com/join-us/reasonable-accommodations.html
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