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Senior Scientist II, Occupational & Environmental Toxicologist

AbbVie
Full-time
Remote friendly (North Chicago, IL)
United States
$106,500 - $202,500 USD yearly
Clinical Research and Development

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Role Summary

Senior Scientist II, Occupational & Environmental Toxicologist. The candidate will complete risk assessments supporting occupational, environmental, manufacturing, and regulatory filings. 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.

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 PDEs and OELs, and environmental risk assessments (ERA), and other contaminants.
  • Collaborate with multi-functional teams to align on safety banding for implementation throughout the company.
  • Engage in external working groups to help drive industry standards and stay informed of upcoming regulations.
  • Provide guidance and mentorship to junior team members in GEO Tox and adjacent departments.
  • Plan and monitor studies at contract research organizations (CROs) for environmental assessments and biocompatibility studies to support regulatory filings.
  • Plan and monitor studies at contract research organizations (CROs) for worker safety studies to occupational safety.
  • Support evaluation/implementation of relevant new approach methodologies (NAM).
  • Provide technical support for occupational health (hazard) categorizations and chemical registrations, including GHS/CLP, and Safety Data Sheets (SDS).

Qualifications

  • Bachelor’s Degree and typically 12+ years of experience, OR Master’s Degree and 10+ years of experience, OR PhD and 4 years of experience.
  • Previous experience in a pharmaceutical/biopharmaceutical or GMP/GLP industry setting providing risk assessments preferred.
  • Proven record of successfully evaluating safety risks.
  • Excellent collaboration, multi-tasking, and communication skills.
  • Excellent writing skills and attention to detail with work.
  • Ability to work in a fast-paced environment and meet project deadlines.

Skills

  • Occupational Exposure Banding, performance-based exposure control limits, or evaluating toxicity data for Safety Data Sheets.
  • Risk assessment authoring.
  • In-depth knowledge and experience with regulatory guidance (ISO-10993-X, ICH Q3C/D/E).
  • Toxicity data mining in databases and literature (internal and external).
  • Broad range of software proficiency and in silico predictive tools for toxicity.
  • Board-certification preferred but not required.
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