No Relocation Assistance Offered
Job Number #167571 - Piscataway, New Jersey, United States
ColgatePalmolive invites applications for a Toxicologist position. The responsibilities of this role will be to provide technical expertise in safety assessments for ingredients, formulas and packaging and will develop strategies to complete special projects. In addition, this position will work closely with internal entities such as the Product Development, Legal and Regulatory departments as well as external groups including subsidiaries, trade associations and governmental agencies to ensure product safety. Successful candidates will demonstrate a broad knowledge of toxicology and its application to ingredient safety assessments and provide safety clearance reviews for: 1) formulas for national launch, 2) experimental formulas in the pilot plants and 3) human use protocols from a product safety perspective.
While this role is predominantly remote, the selected candidate needs to commute to Piscataway, NJ on rare occasions (approximately once a month) at their own cost. Therefore local candidates are encouraged to apply.
Specific Responsibilities:
Conduct safety assessments of new raw materials used in Colgate's formulas including assessment of the scientific literature, evaluation of the toxicological database, determination of the appropriate toxicological endpoints, exposure assessments, and written documentation.
Prepare Product Safety Reports for Colgate's Finished Products.
Communication of Product Safety positions to key internal customers, including, Product Development, Consumer Affairs, Legal Department, Government Affairs, and Regulatory Affairs.
Representation of Colgate's key business interests on trade association task forces.
Respond to regulatory inquiries as requested by the legal authorities in the local countries in which Colgate has products in the marketplace.
Basic Qualifications:
Ph.D. in Toxicology or Pharmacology.
0-3 Years of Experience in Product Safety/Toxicology with a consumer products, medical device, food, or pharmaceutical company.
0-3 years of experience conducting risk assessments of new chemicals/ingredients.
0-3 years of experience preparing safety dossiers for regulatory submissions.
0-3 years developing and implementing strategy to address regulatory toxicology issues.
Preferred Qualifications:
Diplomate of the American Board of Toxicology.
Knowledge of alternatives/in vitro testing/in silico prediction.
Experience setting up and monitoring testing with outside contract labs.
Compensation and Benefits
Salary Range $94,000.00 - $133,000.00 USD
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