Senior Scientist II, Product Safety & Toxicology, L''Oréal Research & Innovation L'Oreal USA IncSenior Scientist II, Product Safety & Toxicology, L''Oréal Research & InnovationClark, NJ$90,200–$135,000 / yearA Day in the Life: As a Senior Scientist II in Product Safety & Toxicology, your responsibilities include: Expert Safety Assessments: Conduct robust safety assessments on raw materials and finished formulations for specific categories (e.g., Skin, Hair, Makeup, or Fragrance), including over-the-counter (OTC) products, ensuring they meet all global regulations. Cross-Functional Data Integration: Collaborate across the organization to ensure sufficient supporting data-including in silico, in vitro, and clinical safety studies-is developed and executed to substantiate the safety of our innovations.
Director, Study Quality and Compliance - Nonclinical Safety/Toxicology Novartis AGDirector, Study Quality and Compliance - Nonclinical Safety/ToxicologyEast Hanover, NJ$185,500–$344,500 / yearThis team is responsible for: handling samples and data associated with both internally and externally conducted toxicology studies; maintaining departmental SOPs, and oversight of training records for departmental personnel; and interfacing with the archives function to ensure proper storage of toxicology-related materials and records. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-cultureBenefits and Rewards: Learn about all the ways we'll help you thrive personally and professionally.
Sr. Scientist, Toxicology Legend Biotech CorpSr. Scientist, ToxicologySomerset, NJ$127,313–$167,099 / yearHeadquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. We also provide voluntary commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.
NewPostdoc Associate -Pharmacology & Toxicology Rutgers The State University of New JerseyPostdoc Associate -Pharmacology & ToxicologyNew Brunswick, NJThe candidates will focus on one or two of the following projects: Developing predictive toxicity models for assessing new environmental pollutants, nanoplastics, and environmental mixtures; Developing pharmacokinetic (PK) models for predicting new drug candidates; Curating and managing unstructured or semi-structured health reports, patient records, and other public clinic outcomes using advanced data analytic techniques. Under Policy 100.3.1 Immunization Policy for Covered Individuals, if employment will commence during Flu Season, Rutgers University may require certain prospective employees to provide proof that they are vaccinated against Seasonal Influenza for the current Flu Season, unless the University has granted the individual a medical or religious exemption.
Principal Scientist I/II, Study Quality and Compliance - Nonclinical Safety/Toxicology Novartis AGPrincipal Scientist I/II, Study Quality and Compliance - Nonclinical Safety/ToxicologyEast Hanover, NJ$119,700–$222,300 / yearEssential Requirements: Degree in biological related sciences8+ years of relevant experience working in a pharmaceutical settingExperience working in GLP setting, and general regulatory compliance and animal welfare knowledge related to conduct of toxicology studiesGood communication skills, and excellent logistical/planning skillsFluent in English (spoken and written)Desirable Requirements: Previous experience with SEND packages is desirablePrevious experience with software for online information and program management is a plusThis is a dual level posting. Support SEND package creation and quality review for FDA submissionsSupport the Study Quality and Compliance team's effort for tracking and managing study-related information through input of information types from the areas of responsibility above and generally support the effort in various workstreams or initiatives.
Associate Director, Toxicology Protagonist TherapeuticsAssociate Director, ToxicologyNewark, New JerseyThe Company also has a number of preclinical stage drug discovery programs addressing clinically and commercially validated targets including an oral IL-17 peptide antagonist, obesity dual and triple agonists, an oral hepcidin functional mimetic, and the recently announced IL-4 and amylin programs. Associate Director, Toxicology, Nonclinical Development (Program Toxicologist) Position Description: Protagonist Therapeutics is seeking a talented, highly motivated professional to join the Toxicology, Nonclinical Development team as Associate Director Toxicology, Nonclinical Development (Program Toxicologist).
Study Manager, Toxicology Revolution Medicines IncStudy Manager, ToxicologyNYRemote$129,000–$160,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. Coordinate study-related activities between RevMed personnel (toxicologists, Project Management, CMC, Bioanalytical, Regulatory, Finance, and Legal groups), and CROs to ensure program needs and timelines are met.
Study Director III, Toxicology InotivStudy Director III, ToxicologyMt. Vernon, IndianaThis position requires a bachelor’s degree and 10 years of relevant experience, or a master’s degree and 5 years relevant experience, or a doctoral degree in one of the biological sciences and at least 2 years relevant laboratory animal experience. Frequent involvement with radiant/electrical energy, solvents, grease, oil, irritants, acids, bases, and other hazardous chemicals, electro-mechanical hazards, flammable materials, and biohazards.
Senior Toxicologist Regeneron PharmaceuticalsSenior ToxicologistTarrytown, NY$128,600–$210,000 / yearToxicologist will demonstrate a thorough understanding of GLP regulations and FDA/EMEA/ICH nonclinical safety guidelines to independently lead the design, conduct, interpretation, and reporting of regulatory toxicology and/or exploratory pharmacology/toxicology studies in rodent and non-rodent safety models. The Senior Toxicologist utilizes their scientific expertise and regulatory experience to lead nonclinical development programs with guidance from her/his direct supervisor working effectively within cross-functional project teams.
Chemist/Toxicologist Part Time/Limited Duration Consumer Reports IncChemist/Toxicologist Part Time/Limited DurationYonkers, NY$65,000–$70,000 / yearAs a Chemist/Toxicologist Senior Project Leader on our Product Safety team, you will report to the Product Safety Manager and focus on the analysis and interpretation of chemical contaminant data across consumer product categories to identify hazards and assess human health risks. Our food and product safety tests are conducted here using state-of-the-art equipment that, when combined with data, allow us to provide expert advice to consumers on topics such as lead found in a popular blender or problems we found when testing a baby stroller.
Senior Scientist, Sterile Product Development (On-site) Merck & Co IncSenior Scientist, Sterile Product Development (On-site)Rahway, NJ$117,000–$184,200 / yearRequired Skills: Biologics, Bioprocessing, Characterization Techniques, Data Analysis, Drug Delivery, Drug Formulations, Drug Product Development, Molecular Biology Techniques, Pharmaceutical Process Development, Pharmaceutical Sciences, Product Formulation, Protein Biochemistry, Protein Purifications, Stability Studies, Sterile Products. Biologics formulation design/process development, alternative processing approaches, definition of critical attributes for process scale-up, analytical development and Chemistry, Manufacturing and Control filing for sterile dosage forms including ocular dosage forms, peptide therapeutics, and non-conventional drug delivery technologies (e.g.
NewToxicologist NAMSA IncToxicologistNY$83,500–$162,900 / yearQualifications & Technical Competencies: Bachelor's degree or equivalent experience in a related field, and a minimum of 5 years of relevant experience; or Masters or Doctorate degree, and a minimum of 2 years of relevant experience required. Please Note: Individual base pay depends on various factors, in addition to primary work location, such as complexity and responsibility of role, job duties/requirements, and relevant experience and skills.
Distinguished Scientist, Safety Assessment Project Expert SanofiDistinguished Scientist, Safety Assessment Project ExpertMorristown, NJ$178,500–$257,833.33 / yearThese activities entail formulating the nonclinical safety strategies, designing safety pharmacology and toxicology studies, authoring regulatory documents, being a member of an integrated Project Team, interacting with internal and external partners, and interacting with and responding to global regulatory agencies. Our Team: The candidate will be part of a dynamic interactive Preclinical Safety group that spans all aspects of the drug development value chain providing toxicology and safety pharmacology expertise as a member of global project teams.
Associate Director, Pharmacovigilance/ Product Safety Insmed IncAssociate Director, Pharmacovigilance/ Product SafetyNJRemote$179,000–$232,500 / yearFor New York City Residents: To assist in identifying candidates with qualifications matching those required and/or preferred for this role, Insmed uses an Automated Employment Decision Tool ("AEDT") that employs artificial intelligence to analyze and score information provided in resumes and application materials including, but not limited to, skills, work experience, education, and job-related qualifications. Author, review and provide input and approval for drug-safety related regulatory reports and clinical study documents including clinical study protocols, Informed Consent Forms, Investigator Brochures, Integrated Summary of Safety (ISS), Integrated Summary of Efficacy (ISE), MedDRA coding of AEs, product package and labeling.
VP, Head Of Preclinical Development Legend Biotech CorpVP, Head Of Preclinical DevelopmentSomerset, NJ$294,483–$386,511 / yearLead preclinical science for novel modalities including lentiviral vector-based in vivo CAR-T, ex vivo cell therapies, and gene-modified immune cell platforms, with deep understanding of the unique preclinical characterization requirements of each. We also provide voluntary commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.
VP, Head of Preclinical Development Legend Biotech CorpVP, Head of Preclinical DevelopmentSomerset, NJ$294,483–$386,511 / yearHeadquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. Lead preclinical science for novel modalities including lentiviral vector-based in vivo CAR-T, ex vivo cell therapies, and gene-modified immune cell platforms, with deep understanding of the unique preclinical characterization requirements of each.
Assistant Professor- Tenure Track - Sustainable Biology and Environmental Science Seton Hall University, New JerseyAssistant Professor- Tenure Track - Sustainable Biology and Environmental ScienceSouth Orange, New JerseyMore specifically, the hire would be expected to (1) run a core biology courses & support the biology majors in all sciences; (2) increase the variety of upper-level bio-electives by offering new courses such as Sustainable Agriculture and Habitat Restoration or Environmental Toxicology and participate in the ongoing creation of academic programs in Environmental Science; (3) assist with educating, managing, mentoring, and advising the increased number of biology majors; (4) provide a computational based research space for undergrads and graduate students; (5) assist with all the day today activities that are important to a functional department; and (6), just as importantly, the faculty member will participate in innovative, collaborative program development in interdisciplinary STEM fields as part of our “STEM Initiative.” Seton Hall University invites applications for a full-time tenure track professor at the rank of Assistant Professor in the Department of Biological Sciences to start Fall 2026, pending final budgetary approval.
Director, Nonclinical Development Organon & CoDirector, Nonclinical DevelopmentFlorham Park, NJ$152,300–$259,200 / yearSupport Regulatory activities for global products such as, annual reporting of nonclinical activities and literature, support new regional drug applications, regional license renewals, author responses to questions from global Heath Authorities. This position will report to the Executive Director, Translational Sciences and Nonclinical Development and work collaboratively with early clinical development, late-clinical development, regulatory affairs, safety and pharmacovigilance, chemistry, manufacturing and control (CMC), medical affairs and business development as necessary.
Senior Clinical Lead, Early Clinical & Experimental Therapeutics SanofiSenior Clinical Lead, Early Clinical & Experimental TherapeuticsMorristown, NJ$236,250–$393,750 / yearIn these roles, duties include: Design safe, rapid and informative First-In-Human studies for oncology assets potentially including natural history, experimental model validation, mechanistic and signal seeking, streamlined Proof-of-Mechanism as well as Proof-of-Concept studies providing robust data for early Go/No Go decisions and other pharmacokinetic studies. A key focus of this role is to support the path from the research phase through early clinical development including early and rapid Proof-of-Mechanism/Proof-of-Concept, as well as natural history studies and experimental model validation to contribute to Human Target Validation (HTV) and evaluating the pharmacology of novel therapeutic approaches.
NewVP, Head of Preclinical Development Legend Biotech USVP, Head of Preclinical DevelopmentSomerset, New JerseyLead preclinical science for novel modalities including lentiviral vector-based in vivo CAR-T, ex vivo cell therapies, and gene-modified immune cell platforms, with deep understanding of the unique preclinical characterization requirements of each . We also provide voluntary commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.