Toxicologist Resume Samples

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I Leuschke

Itzel

Leuschke

543 Reinger Parkway

Chicago

+1 (555) 909 7816

543 Reinger Parkway

Chicago

Phone

p +1 (555) 909 7816

Experience Experience

Houston, TX

Toxicologist

Houston, TX

Lemke-Steuber

Houston, TX

Toxicologist

Work proactively with cross-functional teams to ensure product safety is considered early in the development process
Coordinate and perform data analysis and prepare test reports
Working knowledge of Good Laboratory Practices regulations
Analyze and evaluate problems to develop sound experimental techniques for scientific studies
Design and manage toxicology research under Good Laboratory Practices (GLP) regulations
Design and manage toxicology research as a Study Director/Principal Investigator
Responsible for providing non-clinical safety support to in-licensing review teams

Houston, TX

Staff Toxicologist

Houston, TX

Nikolaus-McLaughlin

Houston, TX

Staff Toxicologist

Guides and develops the technical foundations of policies, procedures and initiatives to ensure development of consistent processes
Integrate with multiple functions across Boeing, including engineering, supplier management, Legal, government affairs, internal governance, etc
Participate in the proposal and bid development process
Proactively identify future biological safety challenges and develop strategies to address them
Perform other duties as assigned
Work Collaboratively with scientists, engineers, and regulatory specialists in multidisciplinary project teams
Review product safety data, identify gaps and perform risk analyses

present

New York, NY

Senior Toxicologist

New York, NY

Connelly-Klocko

present

New York, NY

Senior Toxicologist

present

Providing technical guidance to other 3M staff groups involved with regulatory and hazard communication issues for assigned businesses
Development of recommendations and draft reports
Development of technical publications, presentations at conferences, and proposal sections
Development of tools, guidance materials, and other resources
Review of work produced by others
Critical analysis and evaluation of toxicology studies, including study quality determination and identification of studies for dose-response analysis
Determination of chemical mode of action, including adverse outcome pathways

Education Education

Bachelor’s Degree in Toxicology

University of Oregon

Bachelor’s Degree in Toxicology

Skills Skills

Ability to prioritize, multi-task, and work under strict deadlines in a fast-paced environment
Strong analytical skills
Strong written and oral communication skills
Excellent organizational and time management skills
Attention to detail
Be able to contribute positively to the social environment in the department
Demonstrate excellent presentation and communication skills and build trust with colleagues and stakeholders
Be a team-player while still having a strong drive to push forward and create results within tight deadlines
Proactive and problem-solving approach to challenges
Experience with addressing Adverse Outcome Pathways using in vitro techniques would be considered an advantage

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15 Toxicologist resume templates

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Toxicologist Resume Examples & Samples

Research and data collection using peer-reviewed literature, on-line data sources, technical reports, and other sources
Critical analysis and evaluation of toxicology studies, including study quality determination and identification of studies for dose-response analysis
Determination of chemical mode of action, including adverse outcome pathways
Synthesis of information from multiple data streams (i.e., in vivo and in vitro) to support hazard, dose-response, and risk conclusions
Identification and analysis of data gaps
Development of recommendations and draft reports
Development of tools, guidance materials, and other resources
Interaction and correspondence with clients
Review of work produced by others
Development of technical publications, presentations at conferences, and proposal sections
Mentoring and training other technical staff
Advanced degree in toxicology, pharmacology, physiology, biochemistry, molecular biology, environmental health or related subject with focus on human health hazard and risk assessment
PhD plus 2 years of experience or Master’s degree plus 5 years of experience
Experience assessing human health impacts of chemicals
Experience with government regulatory programs (preferably U.S. EPA)
Proactive and problem-solving approach to challenges
Strong analytical skills
Strong written and oral communication skills
Excellent organizational and time management skills
Attention to detail
Ability to prioritize, multi-task, and work under strict deadlines in a fast-paced environment

Senior Toxicologist Resume Examples & Samples

Research and data collection using peer-reviewed literature, on-line data sources, technical reports, and other sources
Critical analysis and evaluation of toxicology studies, including study quality determination and identification of studies for dose-response analysis
Determination of chemical mode of action, including adverse outcome pathways
Synthesis of information from multiple data streams (i.e., in vivo and in vitro) to support hazard, dose-response, and risk conclusions
Identification and analysis of data gaps
Development of recommendations and draft reports
Development of tools, guidance materials, and other resources
Interaction and correspondence with clients
Review of work produced by others
Development of technical publications, presentations at conferences, and proposal sections
Mentoring and training other technical staff
PhD in toxicology, pharmacology, physiology, biochemistry, molecular biology, environmental health or related subject with focus on human health hazard and risk assessment
10+ years of experience
Experience assessing human health impacts of chemicals
Experience with government regulatory programs (preferably U.S. EPA)
Proactive and problem-solving approach to challenges
Strong analytical skills
Strong written and oral communication skills
Excellent organizational and time management skills
Attention to detail
Ability to prioritize, multi-task, and work under strict deadlines in a fast-paced environment

Senior Toxicologist Resume Examples & Samples

10-15 years related experience
Graduate training and experience in Industrial Toxicology (DABT certified, preferred)
Documented skill in quantitative risk assessment of chemicals and materials
Documented skill in structure activity analyses and predictions
Documented experience in the review, assessment and application of toxicology studies in both humans and animals. Documented understanding of global regulations applicable to materials and chemicals
The ability to understand business and apply these technical skills to IBM's global operations

Principal Toxicologist Resume Examples & Samples

The incumbent will document and provide accurate hazard identification, exposure characterization, safety assessment and product safety guidance for medical devices and consumer products globally (with a primary focus on medical devices in the North America region). The incumbent is required to design, communicate and implement product safety strategies in alignment with regulatory strategies and quality systems for new products and represent the GPS department on multi-functional technology, product development, and post-market support teams. The incumbent will author and communicate product safety and regulatory toxicology compliance information, safety point-of-view papers and human health risk assessments to internal and/or external technical experts, regulatory reviewers as well as functional and business unit leaders and management
The incumbent will lead and/or manage the design, monitoring and interpretation of chemical characterization analyses, pre-clinical toxicology, biocompatibility and microbiological safety studies conducted under Good Laboratory Practices (GLP), and when applicable, clinical studies conducted under Good Clinical Practices (GCP). The incumbent will document, author and disseminate human health safety (risk) assessments taking into consideration identified hazard, user or patient exposure according to intended product use or foreseeable misuse
The incumbent will participate in the life-cycle management of KCC medical devices and consumer products globally (with a primary focus on medical devices in the North America region) through the review of post-market surveillance data and other information as gathered by or disclosed to Kimberly-Clark. This may result in the incumbent developing responses to safety-related internal or external customer inquiries and the development of safety-related statements, policies or other documentation for internal or external distribution in collaboration with Regulatory, Medical Sciences, Quality, Corporate Communications and/or Legal
The incumbent is expected to understand and anticipate business unit requirements and/or needs and work collaboratively with the product development and manufacturing communities and other compliance functions such as Quality, Regulatory, Clinical Affairs, Medical Sciences and Legal. He/she is expected to effectively communicate assessments or scientific information to technical, program management and business communities. If necessary, he/she is required to effectively communicate and advocate product safety-related positions and influence scientific thought with global regulatory bodies, Key Opinion Leaders, non-governmental organizations, and trade associations and in support of potential litigation situations
The incumbent will conduct themselves in accordance with expected Kimberly-Clark leadership behaviors and corporate policies and procedures with an expectation to maintain and enhance their technical, professional, leadership and communication skills through continuing education and professional development courses, attendance and participation in scientific conferences and meetings, publication of appropriate work in peer-reviewed journals and other aspects of technical and leadership development. He/she will also participate on cross-departmental teams to contribute to the development or revision of departmental policies and procedures
Degree in toxicology, biomedical or related field of relevant product safety experience in the design, development, regulatory clearance/approval and maintenance of medical devices in global markets
O Bachelor’s degree with 7+ years of experience, or
Demonstrated ability or willingness to develop subject matter expertise in microbiology/microbial sciences and women’s health
Strong interpersonal skills, technical leadership and demonstrated proficiency as an effective contributor to research or product development teams. Demonstrated ability to independently manage multiple projects in a corporate setting and the ability to effectively communicate in written or oral presentation formats
Ability to travel up to 20-30% (domestic and international)
LI-POST

EPA Environmental Toxicologist Resume Examples & Samples

M.S. or Ph.D. in Environmental Toxicology, Ecotoxicology or related field
Minimum of 7 years experience
Experience with FIFRA
Experience with environmental exposure and risk assessment for pesticides
Research publications in peer-reviewed journals related to ecotoxicology

Investigative Toxicologist Resume Examples & Samples

Assist in developing and delivering an over-arching strategy for the delivery of toxicology, which may include internal resource and/or external partners
Aid in the development of a forward facing vision of the non-clinical sciences department, and support implementation of this vision
Provide internal expertise to understand the mechanisms of toxicity observed non-clinically and/or clinically in order to drive mitigation and/or back up strategies to minimize harm to patients
Build collaborative networks internal and external to the company to ensure rapid communication and cross functional investigation of emerging safety issues
Present data and interpretations in written and oral form to regulatory bodies to enable optimal clinical development and registration of novel drugs
Act as a non-clinical team representative responsible for the non-clinical safety strategy of novel target/therapeutic candidates. Your ability to understand the toxicity of the platform versus target related toxicities is key
Develop strong knowledge of the basic biology of the intended target of drug candidates
Represent Seattle Genetics in the external scientific environment – influencing partners and regulators in a positive way
DABT (or equivalent)
PhD
Proven success in scientific investigation of fundamental biology questions, either through scientific publications or drug development experience

Toxicologist Resume Examples & Samples

Planning toxicology operations in support for a given project
Organizing and monitoring toxicology studies done in CRO
Writing and organizing the preclinical dossier of submission in a given project
Lead multidisciplinary pre-clinical activities in given projects
A high academic degree (Ph.D., or equivalent) in Toxicology, Pharmacy, Pharmacology, DVM or a related field
Excellent verbal and writing communication skills
Experience in Industry as a toxicologist
Knowledge of regulatory toxicology and of the submission process
Preferably an accredited or registered toxicologist
A good understanding of related preclinical disciplines (e.g, ADME, Pharmacology, Biological Method Development)
Ability to lead multidisciplinary teams in a matrix organization

Toxicologist Resume Examples & Samples

Design and manage toxicology research as a Study Director/Principal Investigator
Design and manage toxicology research under Good Laboratory Practices (GLP) regulations
Analyze and evaluate problems to develop sound experimental techniques for scientific studies
Coordinate and perform data analysis and prepare test reports
Present data at client meetings or conferences
Train and mentor junior technical staff
Prepare cost and schedule estimates on proposed projects/assays in toxicology
Work around or with hazardous materials may be required and would be performed by following all safety guidelines to minimize exposure
DABT Certification
Experience working with extremely hazardous chemicals/biologicals
Knowledge of US Army rules and regulations surrounding chemical/biological agent operations
Understanding of GLP and ISO regulations

Product Stewardship Toxicologist Resume Examples & Samples

Master's degree in related discipline
5 - 10+ years of related work experience
Chemical or allied industry experience
Knowledge of industrial organic chemistry
Regulatory affairs/product safety experience
PhD is highly preferred
Regulatory experience in industrial chemicals and polymers is preferred

Principal Scientist Regulatory Toxicologist Resume Examples & Samples

Integration of toxicology, human food safety, target animal safety, user safety and environmental assessments into submission documents
Response to regulatory queries (Global)
Toxicological assessments for residual solvents, excipients, impurities in the manufacturing process
Medical assessments supporting pharmacovigilance and product quality
User safety support for project teams (writes the documents, assembles various scenario calculations and risk mitigation proposals, packaging choice, label language)
Safety Expert Reports for registration renewals
Manufacturing: May aid in assessment of out of specification batches, segregation assessments, cleaning limits
Environmental Risk Assessments: potentially work with environmental risk assessments including project strategy, document preparation, contracting and monitoring studies, study report review
Occasional travel: <15% depending upon study involvement
PhD (or equivalent) plus at least 5 years of experience in a related field such as toxicology, pharmacology, environmental science is critical
Demonstrated skills in technical writing (protocols, reports, journal articles)
Some experience in writing regulatory toxicology and/or environmental safety dossiers, as well as experience in the design, implementation, and interpretation of studies evaluating in vivo toxicity or similar experience would be expected
The candidate should have excellent organizational and communication (verbal and written English) skills, and the ability to work and be effective in a demanding team environment of a global company
Board certification in toxicology
Knowledge of global regulatory requirements for the preparation of toxicology to support human food safety filings, and user safety assessments
Some familiarity with environmental assessments and with internationally accepted mathematical models used to predict concentrations of product active ingredients in the environment would be strongly considered
Experience in conducting studies in a regulated environment (GLP-compliance) is desirable

Senior Toxicologist Resume Examples & Samples

Providing division toxicology support to assigned 3M business units, particularly health care businesses, including technical guidance to product development and product responsibility teams, preparation of hazard/risk assessments and coordination of toxicity testing
Serving as Study Monitor for toxicology studies on 3M chemistries/products at contract research laboratories
Communication of toxicity testing and risk assessment results to internal, as well as external customers and scientific/regulatory groups through oral presentations and written reports/publications globally
Providing technical guidance to other 3M staff groups involved with regulatory and hazard communication issues for assigned businesses
Other duties as assigned
Master’s degree or higher from an accredited university
Minimum of five (5) years’ experience related to the conduct/design of mammalian toxicology studies and/or human health risk assessment
Ph.D. in Toxicology, Pharmacology or closely related discipline from an accredited university
Minimum of ten (10) years of applicable toxicology experience
Strong chemistry background also preferred
Board certification (DABT or equivalent)
Experience with evaluation of medical devices, drugs, combination products, and food safety products according to US and international regulatory standards, such as ISO 10993
Experience as a toxicology study monitor at contract research laboratories
Experience with the human health hazard evaluation/risk assessment process for new chemistries
Experience communicating toxicology results or human health hazard/risk assessments through both oral and written methods
Experience/Ability to work in a multi-disciplinary environment with good analytical, interpersonal, and professional judgment skills
Excellent written, verbal communication skills and strong organizational abilities
3M is an equal opportunity employer. 3M will not discriminate against any applicant for employment on the basis of race, color, national origin, religion, sex, sexual orientation, gender identity, age, disability, or veteran status

Drug Development Toxicologist Resume Examples & Samples

Plan and manage nonclinical development activities for drugs, biologics, or devices for clients
Assist senior staff in providing nonclinical and toxicology guidance for client projects
Prepare planning, strategy, summary documents, etc. for use in communicating with Sponsors
Prepare or assist in preparation of nonclinical sections of regulatory documents and INDs
Working with a project manager, ensure maintenance of each development program’s applications, documentation, per regulations
Ensure CRO and consultant deliverables and activities are prepared or conducted on time and of high quality
Review study protocols, reports and related documents for compliance with regulatory requirements and good scientific principles
Act as Study Monitor or Sponsor representative for contracted nonclinical studies
Ensure compliance with GLP, GMP, and regulatory guidelines
BS degree in toxicology, biology, chemistry or related field with 6 or more years of experience, MS with 3 or more years of experience, or PhD with 0 or more years of experience in drug development activities. DABT certification a plus
Experience managing and/or monitoring nonclinical development activities, reviewing/writing protocols and study reports
Excellent oral and written communications skills and ability to communicate effectively with external clients
Awareness of or experience with regulatory submissions including IND briefing documents and IND applications
Solid understanding of GLP requirements and ICH guidelines
Demonstrated ability to work as a member of multiple project teams, and negotiate and achieve consensus in diverse groups
Ability to prioritize and multi-task concurrent project demands
Must be legally authroized to work in the United States and not require sponsorship now or in the future

Human Health Toxicologist Resume Examples & Samples

Review and evaluate toxicological data from laboratory studies for possible use in developing threshold values
Write technical reports and summaries of toxicological reviews and analyses
Evaluate analyses of human health data for purposes of developing threshold value
Education to include a degree(s) in toxicology, epidemiology, statistics, or related scientific disciplines relevant to human health risk assessment
Experience characterizing dose-response relationships, including benchmark dose modeling, specialized cancer modeling, and dose-response modeling of epidemiological data is a plus
Candidates with Board Certification in General Toxicology are preferred

Corporate Toxicologist Resume Examples & Samples

Assess APIs, intermediates, impurities for allowable daily exposure (ADE) / permitted daily exposure (PDE) according to guidelines of FDA / EMA in close cooperation with Quality Assurance (QA). Write and sign formally correct scientific reports
Assess APIs, intermediates, impurities for allowable occupational exposure levels (OEL) such as AHSK (Arbeitshygienische Stoff-Kategorie) in close cooperation with Occupational Hygiene Visp. Write comprehensive rationale
Document all correspondence, findings and reports in CISWEB EHS AHSK Database and in corresponding chemical substance folder

Discovery Toxicologist Resume Examples & Samples

Provide pharmaceutical drug project teams with expert advice and direction to improve the quality of therapeutics selected for further development based on proactive risk assessment of target- and chemotype-related toxicities
Develop comprehensive safety target reviews with risk mitigation plan for early drug discovery project teams based on literature, bioinformatics, and other predictive tools
Apply state of the art in silico and in vitro de-risking strategies to aid in the selection and optimization of large and small molecule therapeutics
Lead the development of early hypothesis-driven investigation into mechanisms of toxicity for the proactive management of potential safety liabilities and communication of impact to teams
Minimum of MS with 8 years of pharmaceutical experience or PhD in a scientific discipline with 3 years postdoctoral experience and/or 5+ years of experience working at a pharmaceutical company
Passion to decrease safety related attrition in drug discovery
Demonstrated experience and ability to work effectively in a matrix, global environment as part of a multidisciplinary team
Broad scientific knowledge including pharmacology, toxicology, pathology, physiology and biochemistry
Strong interpersonal and organizational skills
Excellent oral and written communication skills

Principal Global Mammalian Toxicologist Resume Examples & Samples

Provide team leadership, technical expertise, and strategic oversight of contract laboratories to ensure high quality data, sustainable scientific databases, effective interpretations, toxicology recommendations,and advocacy documents for insecticides, herbicides, fungicides, and biological products
Provide leadership, sound decision-making, project management, personnel support, and career development for Toxicology Team members located in USA, UK, and Denmark
Foster teamwork and collaborations, yet also provide individual contribution and critical-thinking to develop creative mammalian toxicology solutions that meet business objectives
Mentor mammalian toxicology staff and train other Global Regulatory Sciences team members on new toxicology, regulatory, or risk assessment developments
Serve as internal and external mammalian toxicology expert/specialist for broad knowledge to support a portfolio of active ingredients pesticides and biological plant health solutions
Promote sound decision-making needed to develop high-quality, compliant toxicology studies. Be knowledgeable in global toxicology and risk assessment pesticide registration requirements
Conceive, plan and oversee the work of contract research organizations (CRO) for all mammalian toxicity testing to meet global (USEPA, OECD, China, Brazil) regulatory requirements and product safety concerns
Act as Study Monitor of CRO for long term (sub-chronic and chronic) and complex toxicology studies (developmental/repro, mechanism of toxicity) for EPA, EU, and other regulatory agencies including protocol design, test material transmittal, oversight of contract scientists, critical evaluation of data, and working with QA and contract scientists to provide final reports
Review and summarize in-house toxicological study data and literature to prepare critical scientific reviews, chemical hazard and risk assessments, “white paper” advocacy documents, scientific rationales, position statements or monographs for the defense and growth of FMC products. Define and work to resolve major, complex problems coming from interactions of pesticides and a variety of mammalian physiology systems
Make recommendations on path forward in the registration of active ingredients or formulations technologies based upon toxicology data and regulatory requirements. Contribute to the development and execution of product defense strategies using toxicology and physiology knowledge and interactions with other scientific disciplines
Continually pursue creative low-cost, high-value streamlining, and time-centered initiatives for the development of compliant toxicology data
Understand and alert management and business customers about regulatory toxicology initiatives that will shape the regulatory environment for FMC products and our industry
Represent FMC and AGS Toxicology at professional meetings, training and workshops, and industry task forces to maintain and improve technical skills and professional connections. Publish or present scientific information at meetings and in peer-reviewed journals
Broad scientific knowledge in mammalian toxicology, physiology, and/or veterinarian medicineExpert knowledge of toxicology studies (design and interpretation of data generated) required for regulatory Agencies, especially long-term and specialized, complex study types
Experience managing and leading a small, diverse, global scientific team and completing workload to meet tight deadlines and Agency requirements
Strong leadership and interpersonal skills including negotiation, conflict resolution, influencing and motivating
Working effectively within a team environment – leading, exchanging ideas with colleagues, sharing workload, and interacting with upper management
Project management for self and team, including ability to organize, schedule, and prioritize workload and manage external contract scientists, to meet deadlines for concurrent projects
Strong analytical capability to analyze data, process information and provide recommendations to key staff and management
Experience communicating with non-science, business customers and global Registrations Managers and meeting their expectations
Excellent oral and written communication skills, including scientific reports, hazard evaluations, and position papers. Computer literate, experience with Microsoft Office products
Track record of effective interactions with Regulatory agencies in the US, Europe, or globally through white papers or in-person meetings
Knowledge and use of human health and worker Risk Assessment Models
Ability to work with senior management to manage resources and meet timelines
Strong commitment to and awareness of safety practices

Staff Toxicologist Resume Examples & Samples

Participate in the proposal and bid development process
Serve as a key contact for sponsors
Participate in and coordinate all phases of the study planning process with Client Services and technical and laboratory support operations
Responsible for study design and generation of protocols
Interpret study data
Develop and foster business relationships
Post Doctoral experience and DABT preferred
Attention to detail and excellent interpersonal and communication skills

Toxicologist Resume Examples & Samples

Support our discovery group in the safety testing of lead compounds, including introduction of new testing paradigms
Design, supervise, interpret, and report in vitro and in vivo nonclinical toxicology IND enabling studies and studies supporting more advanced clinical stages
Participate in the preparation of preclinical texts for worldwide regulatory submissions, including authoring the nonclinical safety components of regulatory dossiers (e.g. IB, INDs, NDAs) and communications as well as responses to inquiries from regulatory agencies
Work closely with internal functional groups such as Pharmacology, ADME-PK, CMC, Regulatory Affairs, Clinical Development, and Program Management, and actively participate in team strategy discussions for drug development programs
Lead teams of preclinical experts in respective projects
Responsible for providing non-clinical safety support to in-licensing review teams
DVM or PhD in pharmacology, toxicology, or related scientific discipline. Board certification (DABT) is a plus
8+ years of relevant industry experience in toxicology, supporting drug discovery, research and development
Proficient knowledge of general toxicology and related disciplines
Experience with in vitro assays utilized in discovery and toxicological assessment
Familiar with regulatory toxicology guidelines, requirements and standards (GLP, OECD, ICH, CTD, etc.) and able develop nonclinical strategies that support clinical development
Experience in authoring nonclinical components of regulatory dossiers
Independent self-starter with the ability to work in a matrixed, cross-functional, team-based drug discovery/development environment
Excellent verbal and written communication skills; ability to communicate clearly and effectively with scientific colleagues and senior management

Staff Toxicologist Resume Examples & Samples

Plan and oversee in-vivo and in-vitro toxicological and biocompatibility studies that comply with national and international standards (ASTM, ISO…)
Review product safety data, identify gaps and perform risk analyses
Respond to notified bodies (FDA, BSI, CFDA, PMDA..) questions in a timely and thorough manner
Write toxicological assessment and biological evaluation reports
Work Collaboratively with scientists, engineers, and regulatory specialists in multidisciplinary project teams
Proactively identify future biological safety challenges and develop strategies to address them
Thorough knowledge of current global toxicological guidelines (USP, JP, Ph., Eur., etc.)
In depth knowledge of ISO 10993 standards
Working knowledge of analytical chemistry
Knowledge of orthopaedic / pharmaceutical industry desired
Ability to work within a multidisciplinary team setting with good interpersonal skills
MS or PhD degree in Toxicology (DABT certification a plus)
5-8 years industrial experience, preferably in contract laboratories

Toxicologist, Product Safety Resume Examples & Samples

Conduct robust safety assessments that meet global regulations on raw materials and finished formulations for a category of products (e.g. Skin, Hair, Make-up or Fragrance) including OTC products
Evaluation of ingredients, raw materials and formulations for internal and external labs based on risk assessments conducted and communicate safety approvals through product specific meetings
Assist with compiling and reviewing of Cosmetic Safety Reports for compliance with EU and other global regulations
Provide appropriate in vitro and clinical safety support for finished products
Conduct literature searches as needed to generate robust safety assessments
Proactively participate in discussions on internal safety positions

Principal Toxicologist Resume Examples & Samples

Consulting industry experience (preferred) with extensive knowledge of toxicology, public health assessments and human health risk assessments related to chemical and microbial risks
Experience with of Australian chemical regulatory frameworks (e.g. NICNAS, APVMA)
Experience providing expert testimony at hearings
High level project and project team management skills
A relevant post graduate qualification in toxicology, public health or a similar field
DABT (desirable) or potential to seek toxicological certification
High industry profile within the public health, regulatory and toxicology/risk practice areas

Senior Project Toxicologist Resume Examples & Samples

Bachelors degree in a relevant scientific discipline
Significant experience (>3 years) as a project toxicologist across a broad range of stages in discovery and development
Non-clinical capability and experience coupled with an understanding of the interrelationships between disposition, safety and on/off target engagement as applied to the identification and articulation of critical needs and deliverables for projects
Experience in influencing scientific strategy and delivery for projects through a breadth of scientific knowledge of Drug Discovery and Development - experience in coaching/mentoring others in this respect
Experience in the application of non-clinical safety knowledge and tools in the integrated design, optimization and selection of quality driven candidate molecules and worldwide regulatory requirements for drug development and registration
Desirable to have experience of overseeing a portfolio of projects with assigned PTMs with variable levels of experience and background capabilities.Ability to work collaboratively in a highly matrixed, global organization
Demonstrated effective interpersonal, communications and negotiation skills for a wide variety of audiences, including senior management
Courage to lead and make tough decisions/strong influencing skills
Logical and independent thinking
Demonstrated high learning agility
Managing and delivering execution across multiple disciplines
Problem solver, innovative, creative with operational delivery solutions
Ability to coach and mentor others
Good judgment and personal flexibility to adapt to changes in R&D priorities
As a PTM (typically covering ≥3 compounds), represent non-clinical safety and potentially disposition (DMPK) on Project teams

Senior Forensic Toxicologist Resume Examples & Samples

Supervise analytical chemists that perform routine drug testing analyses
Provide day-to-day guidance and oversight for specimen accessioning/storage, drug screening/drug confirmation analyses, and data review
Assure that quality standards are followed and that all analyses are performed in accordance with laboratory SOPs and DoD drug testing policies
Certify laboratory results
Oversee method development, method validation and troubleshoot analytical challenges
Perform or delegate instrument maintenance
Assist with the development and implementation of a Laboratory Inventory Management System (LIMS)
Prepare monthly reports for leadership
Serve as a subject matter expert and an expert witness for military litigation proceedings
Perform or delegate immunoassay analyses, colorimetric analyses , spectrophotometric analyses in addition to solid phase and liquid /liquid extractions
Utilize Gas Chromatography/Mass Spectrometry, Liquid Chromatography/Mass Spectrometry, and Tandem Mass Spectrometry
Produce detailed notes and reports
Perform technical and administrative reviews of other analysts’ casework
Interact and collaborate with other group/team members and other forensic staff to ensure a high quality and accurate product
A minimum of a Bachelor of Science degree from an accredited college or university in the Physical Sciences (e.g., Chemistry, Pharmacology, Toxicology) coupled with 5+ years experience working in an accredited Forensic Toxicology laboratory; OR a Master of Science degree in the Physical Sciences (e.g., Chemistry, Pharmacology, Toxicology) coupled with 3+ years experience working in an accredited Forensic Toxicology laboratory
Proficient in Forensic Toxicology with advanced skills in solid phase and liquid/liquid extractions, immunoassays, Gas Chromatography/Mass Spectrometry and other chemistry analytical methodologies such as Liquid Chromatography Tandem Mass Spectrometry
Experience with toxicological casework involving postmortem, human performance, DUI/DUID, drug facilitated sexual assault investigations, and DoD drug demand reduction urinalysis toxicology
Laboratory supervisory / personnel management experience
Proficient working with Microsoft Office Suites, to include excel spreadsheets
Skilled communicator who can clearly articulate/communicate via email, telephone calls and video teleconferencing
Ability to obtain and maintain a DoD Secret clearance
Forensic Toxicology expert witness testimony
First authorship of scientific research in peer reviewed journal and/or presentation of scientific data
American Board of Forensic Toxicology (ABFT) certification
Knowledge and experience with method and instrument validations
Active in the field of Forensic Toxicology (e.g., Society of Forensic Toxicology member)
Familiar with database structure and/or a willingness to learn the necessary skills to configure and modify the Laboratory Inventory Management System (LIMS)

Project Toxicologist Resume Examples & Samples

BS degree in a relevant scientific discipline including aspects of Toxicology/Safety Assessment
Minimum 3 years of relevant experience
Experience as a project team member covering a number of projects across a broad range of stages in development
Safety Assessment capability and experience coupled with an understanding of the interrelationships between disposition, safety and on/off target engagement as applied to the identification and articulation of critical needs and deliverables for projects
Knowledge and experience of the Safety Assessment aspects of worldwide regulatory requirements for drug development and registration
Broad knowledge / experience of drug disposition (ADME) an advantage
MS or PhD in a relevant scientific discipline
Diplomate, American Board of Toxicology or equivalent experience
Ability to work collaboratively in a highly matrixed, global organization
Demonstrated effective interpersonal, communication (written and verbal) and negotiation skills for a wide variety of audiences, including senior management
Demonstrated logical, independent thinking with strong influencing skills and courage to lead and to make tough decisions
Demonstrated high learning agility and ability to effectively manage multiple projects
Demonstrated problem solver, innovative and creative to provide operational delivery and scientific issue solutions
Good judgment and personal flexibility to adapt to changes in R&D priorities

Principal Toxicologist / Director Resume Examples & Samples

Development of appropriate strategies to assess nonclinical safety of MedImmune assets; this includes high level input into designing studies and actively contributing to inclusion of pharmacodynamic readouts in these studies
Organising, planning and data monitoring of in vivo toxicology studies in collaboration with Associate Toxicologists and Toxicologists
Oversee the delivery of reviewed and approved final toxicology study reports, suitable for regulatory submission, in collaboration with Associate Toxicologists and Toxicologists
Contribute to regulatory documents (CTAs, IMPDs, INDs, BLAs, etc); be involved in interactions with regulatory authorities as needed
Communicate toxicology data internally and to Research Project and Product Development Teams, ensuring delivery in line with the business objectives of validity, integrity, quality, timing & cost
Attend and/or present at relevant governance committees, including but not limited to Research Review Committees (RRC), the MedImmune Safety Review Board (MSRB), and the Early and Late Stage Product Committees (ESPC, LSPC)
Identify threats to the nonclinical safety assessment plan, propose options for resolution or mitigation of these threats, and ensure implementation of appropriate adjustments to the nonclinical safety strategy
Act as a key functional expert in the field of nonclinical safety testing of biologics and maintain immunological and toxicological expertise; this includes, but is not restricted to, keeping up todate with the scientific literature, attend and contribute to relevant international meetings, and publish in peer reviewed journals
PhD degree in a relevant subject area
Extensive experience with managing CRO-based toxicology studies, including experience with studies in common toxicology species (rats and especially nonhuman primates)
Proven pharmaceutical industry experience in the field of nonclinical safety testing of biologics
Understanding of the regulatory requirements for the toxicology testing of biologics
Understanding of toxicological mechanisms as the basis of developing safe medicines
Experience with acting as nonclinical safety representative in early stage (lead optimisation-IND-Phase I) as well as later stage project teams (Phase II and beyond) Experience with preparing and submitting regulatory documentation (CTA/IND, briefing documents) and regulatory interactions
Other relevant professional qualifications or recognition, e.g. DABT/ERT
Specialist expertise in a field relevant to nonclinical safety testing of biologics, e.g. immunology/immunotoxicology
Recognised as an industry leader in the field of biologics safety testing as evidenced by publication record and involvement in professional organisation
LI-MEDI

Environmental Toxicologist / Entomologist Resume Examples & Samples

Designing, coordinating, and initiating testing program to characterize activity spectrum, non-target organism effects and ecological risk of new products
Preparing and reviewing ecological risk assessment reports to support registration of biotechnology-derived products
Keeping abreast of scientific and political developments relevant to U.S., OECD, and global regulatory guidelines for environmental safety assessments of plant incorporated protectants
Addressing agency and academic questions around ecotoxicology and ecological risk assessment of products with sound and supported scientific responses
Driving publications in accordance with product strategy
Representing Monsanto’s support for science based environmental risk assessment internally and externally with industry, academia, government and public stakeholders
Driving and leading new considerations/tools for NTO bioassays and ecological risk assessment on case by case basis--e.g. new modes of action
Minimum of Ph.D. in Ecotoxicology or a closely related discipline
Minimum of three or more years of professional experience monitoring and conducting GLP ecotoxicology studies and conducting ecological risk assessments for crop protection products
Functional knowledge of biostatistics, experimental design, exposure assessment, and analytical methodology
Strong project and time management abilities
Agility to work on multiple projects and flexibility to meet business objectives
Self-motivated and capable of functioning as an independent scientist while being able to work effectively in a team environment
Knowledge and/or experience interacting with regulatory authorities and issue management
Direct experience participating in industry task forces and/or work groups
Experience with U.S. and/or EU ecotoxicology test guidelines and risk assessment approaches for crop protection products including endangered species risk assessment
Prior experience leading scientific initiatives across functional areas
Prior experience working for a global company

Medical Toxicologist Resume Examples & Samples

Provide advice and consultation to physician callers or poison center specialists on cases involving severe symptoms, and medical management questions
Provide phone or in person information when possible and/or needed
Other duties and responsibilities include teaching and research
Recent publications in the field of toxicology
Emergency medicine experience
Fellowship in Toxinology (specific to Envenomations)

Clinical Toxicologist Resume Examples & Samples

Provide advice and consultation to physician callers or poison control center specialists on cases involving severe symptoms, and medical management questions
Provide other related information by phone or in person when possible and/or needed
There may be other teaching and research duties assigned as necessary related to this position
Completion of an accredited Toxicology Fellowship
Medical Toxicology Board certified or board eligible

Quantitative Systems Toxicologist Resume Examples & Samples

PhD in Pharmacology, Toxicology, Biochemistry, Mathematics, Engineering, Physics or related disciplines with experience of applying mechanism based mathematical modeling techniques to biological systems. e.g. complex modeling approaches such as descriptive and predictive logic based models, PBPK models or mechanistic modeling in the pharmaceutical industry
Experience working in a computational toxicology/biology environment
Experience with quantitative systems modeling to design and develop new molecules with decreased safety liability
Experience of Scientific computing and programming e.g. experience in MATLAB + SimBiology and/or object oriented programming, together with one or more of the following (a) integration of discovery chemistry, extracting and analyzing decision-making data associated with chemical entities; (b) computational systems biology and toxicology and ability to integrate information at various levels of biological organization (molecular, cellular, organ, animal, population) using the Adverse Outcome Pathway framework; (c) and knowledge of semantic data mining and integration strategies (e.g. ontology’s, text analytics, database and tool interface development, computational chemistry)
Forward thinking, with evidence of scientific curiosity coupled with strong critical thinking, troubleshooting and problem solving skills in systems modeling in drug discovery and development
Demonstrated ability to work in multi-disciplinary teams with excellent interpersonal skills, particularly with regard to building strong working relationships within the computational community and external partners or customers
Excellent written and oral communication skills and the ability to interact effectively with scientists in other disciplines with a positive, collegial, and collaborative attitude
Knowledge of principles driving chemical reactivity and biological processes along with strong analytical skills resulting in demonstrable impact in a pharmaceutical/biotechnological environment
Evidence of commitment to developing self and others
Ability to prioritize amongst competing time demands
Demonstrated skills to programmatically collect, combine, mine and analyze complex biological and chemical data
Experience analyzing ‘omics data and building network models from data
Successfully leads in a matrix environment, working across functions/disciplines
Manages the planning and execution of projects until completion
Entrepreneurial mindset

PHD Eco Toxicologist Resume Examples & Samples

Ph.D. in Eco-toxicology, Toxicology, Ecology, or Environmental Science with 3+ years experience in Environmental Risk Assessments; regulatory and research studies; and product safety/ compliance for agrichemicals, herbicides, pesticides, fertilizers, etc
Background in genetics and/or molecular biology is desirable
Experience working in a team-oriented environment managing multiple projects, possess excellent analytical, interpretive and communication skills, and be able to adapt technical skills to changing needs
A strong capacity for problem solving, planning, organization, and the ability to develop technical skills in disciplines beyond the candidate’s area of expertise
Strong written and verbal communication skills are essential for this position. A high level of advocacy skills and an ability to work with senior scientists
Travel- 15%
Only applicants authorized to legally work in the US without sponsorship can be considered

Staff Toxicologist Resume Examples & Samples

Integrate with multiple functions across Boeing, including engineering, supplier management, Legal, government affairs, internal governance, etc
Guides and develops the technical foundations of policies, procedures and initiatives to ensure development of consistent processes
Represent the company with government agencies, suppliers, customers and industry and trade groups
Support regulatory compliance strategy for imports/exports and bans on chemicals present in our products or used in our manufacturing processes
Be able to effectively analyze complex information and communicate results to all levels within the company
Candidates must possess strong leadership, teaming, communication, project leadership, and computing skills
More than one year of toxicology experience is highly desired
Experience with aerospace operations and services is highly desired
An advanced degree in toxicology (or related field) is highly desired

Environmental Toxicologist Resume Examples & Samples

Collaborates with multidisciplinary teams to assess and communicate environmental risks, perform environmental impact and fate & effects studies, address environmental issues during oil spill response, and identify and provide environmentally beneficial and cost-effective solutions to environmental issues
Typical activities include environmental risk assessment of operations, summary and critical analysis of literature data and regulations, creation and oversight of research programs, and participation in professional organizations and trade associations
Master’s degree in ecotoxicology/environmental toxicology or related environmental science discipline with 5+ years of petroleum industry experience OR Ph.D. in ecotoxicology/environmental toxicology or related environmental science discipline with 3 years of some petroleum industry experience
Broad training in environmental chemistry, fate and exposure assessment, and or ecotoxicology
Demonstrated ability to support Chevron’s Upstream and or Downstream Business Units in applying ecological risk assessment to address issues like discharges to water, ecological exposures and ecosystem health
Experience or ability to support Chevron’s Environmental Management Company project managers in applying ecological risk assessment to address remediation of impacted sites
Experience in lab and field methods used in environmental assessment is a plus, as are strong quantitative skills
Drive to create and actively implement new areas of work that intersect technical abilities and value to Chevron. Interest and ability to identify and implement science and technology R and D to provide innovative, cost-effective solutions to manage environmental risk
Excellent oral and written communication skills, including strong ability to communicate the business implications of environmental risks clearly, concisely and effectively
Demonstrated ability to negotiate with regulators on scientific merits of various approaches/interpretations
Ability to facilitate discussions and build collaborative relationships with diverse and multi-cultural audiences including ETC colleagues; business unit HES specialists and managers; external consultants; regulators; and other stakeholders
Skilled in managing the delivery of high quality, value-added technical HES consulting services that meet customer expectations within agreed budget and schedule including for international customers in different time zones

Staff Toxicologist Resume Examples & Samples

Write toxicological risk assessment and biological evaluation reports
Collaborates with sites to investigate and troubleshoot issues concerning biological safety
Collaborates with sites to align processes, implement best practices, develop metrics and trending data to provide, both site and corporate management timely updates on product quality
Apply toxicological principles to address complex regulatory requirements for product submissions
Monitor regulatory trends, assess business impact to existing and future product lines relating to biocompatibility
Maintain high level of toxicological expertise by identifying and critically assessing emerging theories and methodologies and applying gained expertise to meet research objectives that align with strategic objectives
Knowledge of orthopedic / pharmaceutical industry desired
Demonstrated expertise to effectively communicate within all levels of the organization around concepts of design control, design verification and validation activities; ethylene oxide, irradiation, steam/moist heat and aseptic processing; sterile packaging validation; biocompatibility; production and process controls; cleanroom management and control; Corrective and Preventive Action (CAPA), complaints and risk management; and product quality improvement
Competency in using computer software such as Excel, Word and PowerPoint
Must be willing to travel (approximately 20%)

Associate Toxicologist Resume Examples & Samples

Support existing products and development of new products contributing to safety assessments and regulatory submissions (NDIs, GRAS, FAP, etc
Help to manage contract laboratories conducting nonclinical toxicology studies by designing, reviewing, and finalizing study protocols and reports. You will report to the Principal Scientist of Toxicology & Kinetics
Prepare early safety assessments by literature/databases searches and using in silico tools (predictive QSAR models)
Identify safety profile of candidate compounds / chemical impurities in defined cases
Determine toxicological studies that are required to support regulatory clearances of products and manage the placement and conduct of those studies with contract laboratories
Contribute to experimental design and planning of nonclinical toxicology studies
Ensure compliance of studies in accordance with relevant guidelines and regulation (e.g. OECD/GLP guidelines and applicable FDA regulations)
Monitor studies conducted by CROs, review and finalize study protocols and reports
Analyze data and interpret results with input from senior staff on occasion
Summarize studies reports to be part of regulatory submissions (NDIs, GRAS, FAP, etc.)
Review current scientific literature on an ongoing basis
Present research findings to internal stakeholders
BS with 3-5 years’ experience or MS with 1-2 years of experience in toxicology, pharmacology or in a health or environmental sciences with a major emphasis in toxicology
General toxicology knowledge and expertise in conducting risk assessments
Experience w/ design and planning of nonclinical toxicology studies
Strong technical writing and oral communication skills, as well as excellent organizational skills are essential
Excellent computer skills, including knowledge of most common IT programs as Microsoft Office 2007 (2010)

Toxics Reduction Toxicologist Resume Examples & Samples

Work experience within the fields of green chemistry and/or safer chemical alternative selection is highly preferred
A Ph.D. or Masters of Science degree with a focus on green chemistry and safer chemical alternative selection is highly preferred
Has completed a certificate program in green chemistry and/or safer chemical alternatives (Please see the University of Washington's Green Chemistry & Chemical Stewardship Certificate Program as an example)
Knowledge of industrial processes involving hazardous substances, generation of hazardous or solid wastes, air emissions and wastewater discharges to analyze the technical feasibility of alternative chemicals and reduce hazardous material use at industrial scale
Ability to present technical information (written and through presentation) with clarity to a wide audience
Ability to interact with a wide variety of individuals and exercise communication skills needed to network within Industrial and Toxics Reduction communities
A cover letter describing how your experience, skills and abilities meet the required qualifications of this position
A resume outlining your professional experience