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Toxicologist Jobs
Company | Battelle |
Address | Columbus, OH, United States |
Employment type | FULL_TIME |
Salary | |
Category | Defense and Space Manufacturing,Aviation and Aerospace Component Manufacturing,Biotechnology Research |
Expires | 2023-07-08 |
Posted at | 11 months ago |
Battelle delivers when others can’t. We conduct research and development, manage national laboratories, design and manufacture products and deliver critical services for our clients—whether they are a multi-national corporation, a small start-up or a government agency.
- Follows FDA GLP and other appropriate regulatory (e.g., OECD, ICH) requirements to ensure all experimental data, including observations of unanticipated findings, are accurately recorded and verified.
- In collaboration with the business development team and senior toxicology staff, is responsible for new pipeline development; accountable for some level of revenue generation.
- Oversees the building of new capabilities to bring in new technologies and services.
- Authors, updates, and/or reviews area-specific SOP’s, ensuring that SOP’s reflect current practices.
- Reviews toxicology data and authors toxicology study reports, or portions thereof, as appropriate.
- Participates in all required training.
- Manages studies within time and budget constraints.
- Observes appropriate safety and study requirements by reading, understanding, and following SOP’s, GLP regulations, and study protocols.
- Drafts protocols, amendments, departmental notifications, and study comments forms, ensuring correct grammar, punctuation, consistency in format and style, and adherence to regulatory requirements and contract language.
- Design toxicology studies to develop animal models and then test medical counter-measure efficacy.
- Interfaces directly with client’s scientific staff as appropriate.
- Reviews SOP’s associated with study conduct and incorporates language into the protocol describing procedures or processes when necessary.
- Identifies and incorporates exceptions to GLP conduct into GLP study protocols as applicable (e.g., systems/processes that are not validated).
- Serves as Study Director on toxicology, biodistribution, pharmacokinetic, efficacy, and related studies for commercial and government sponsors.
- Participates in proposal generation and performs scientific/technical review of proposals.
- Reviews and approves Provantis study setups.
- Within defined policies and procedures, provides resolution to complex scientific problems within a specified program.
- Partners with Business Development, Project Management, and Proposals to ensure successful client engagement, proposal development, study execution, and deliverables upon study completion.
- Additionally, will require ability to obtain and maintain the following: DOJ Security Risk Assessment approval, CDC Approval to work with BSAT material, Chemical Personal Reliability Program (NACLC required) and Biological Suitability Assessment Program. Ability to work in biosafety level 2 (BSL2) (biocontainment) and wear appropriate respiratory protection. Requires participation in random drug screening. Willing to be immunized with FDA licensed vaccines and Investigational New Drugs (IND) recommended for persons at risk to occupational exposure of biological agents.
- Must be a US citizen with the ability and willingess to obtain security clearance.
- Expertise in in-vivo design, execution, interpretation of small-molecule toxicology studies.
- Effective verbal and written communication skills including correct grammar, spelling, and punctuation. Prior presentation experience.
- PhD degree in life sciences discipline or Master’s degree with 2+ years prior experience or Bachelor’s degree with 5+ years prior experience.
- Demonstrated competency in regulated environment including prior experience working in a GLP or similarly regulated environment.
- Diplomate of the American Board of Toxicology certified OR DABT eligible – if not already certified, candidate will be required to become board certified within five years of hire date.
- Better together: Coverage for partners, gender-affirming care and health support, and family formation support.
- Build your financial future: Build financial stability with an industry-leading 401(k) retirement savings plan. For most employees, we put in 5 percent whether you contribute or not, and match your contributions on top of that.
- Flexible work arrangements: You have options for where you work and when you work.
- Advance your education: Tuition assistance is available to pursue higher education.
- Take time to recharge: You get paid time off to support work-life balance and keep motivated.
- Balance life through a compressed work schedule: Most of our team follows a flexible, compressed work schedule that allows for every other Friday off—giving you a dedicated day to accomplish things in your personal life without using vacation time.
- Prioritize wellness: Stay healthy with medical, dental, and vision coverage with wellness incentives and benefits plus a variety of optional supplemental benefits.
- Nurture and develop the next generation of scientific leaders
- Apply your talent to challenging and meaningful projects
- Collaborate with world-class experts in an inclusive environment
- Give back to and improve our communities
- Receive select funding to pursue ideas in scientific and technological discovery
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