Senior Regulatory Affairs Specialist Medline IndustriesSenior Regulatory Affairs SpecialistJob Posting Only, IL$92,000–$138,000 / yearFull timeComplete and maintain varied regulatory filings by leading internal groups, collaborating with external groups, evaluating and providing direction on supporting technical information, writing appropriate summary documentation, providing direction on product/project changes, and responding to non-conformances and questions from regulators. Prepare comprehensive regulatory strategies for new devices, new launch markets, and post-market device changes, ensuring that the content, context, organization, and quality of supporting information is sufficient to meet all regulatory requirements, commitments, and agreements.
Sr. Regulatory Affairs Specialist Medline IndustriesSr. Regulatory Affairs SpecialistWork From Home, IL$92,000–$138,000 / yearFull timeComplete and maintain varied regulatory filings by leading internal groups, collaborating with external groups, evaluating and providing direction on supporting technical information, writing appropriate summary documentation, providing direction on product/project changes, and responding to non-conformances and questions from regulators. Prepare comprehensive regulatory strategies for new devices, new launch markets, and post-market device changes, ensuring that the content, context, organization, and quality of supporting information is sufficient to meet all regulatory requirements, commitments, and agreements.
Director of Individual Insurance Compliance & Regulatory Affairs Alera GroupDirector of Individual Insurance Compliance & Regulatory AffairsChicago, IllinoisReporting directly to the Chief Legal Officer with a dotted-line partnership to the SVP of Strategy & Operations, this role will collaborate across Legal, Operations, Marketing, IT, Carrier Relations, and agency leadership to drive consistency, accountability, and audit readiness throughout the organization. This senior leadership role is responsible for building scalable, defensible compliance frameworks that support growth while ensuring regulatory excellence across Medicare, ACA, and ancillary insurance products.
Director, Regulatory Affairs Thermo Fisher Scientific IncDirector, Regulatory AffairsIL$175,000–$219,000 / yearWe provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy.
NewDirector, Regulatory Affairs Jupiter Power LLCDirector, Regulatory AffairsChicago, IL$160,000–$180,000 / yearIn this role, you will be responsible for tracking and communicating regulatory requirements for Jupiter's entities and resources to participate in markets and will be responsible for working closely with cross-functional teams to ensure regulatory developments, project requirements, and market opportunities are effectively analyzed and communicated. Lead regulatory tracking and internal communication of requirements necessary for execution of regulatory activities supporting project development, i.e. filings for capacity market participation, interconnection processes, and other market-related requirements.
Associate Director Regulatory Affairs Advertising & Promotion Hybrid AbbVie IncAssociate Director Regulatory Affairs Advertising & Promotion HybridILThe Associate Director envisions the future by using global marketplace, technology and business knowledge, collects and analyzes issues and trends that affect the business, identifies and acts upon cross-organization or cross-business opportunities and possesses and leverages broad industry knowledge. US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html.
Executive Director of Administration and Finance, Division of Student Affairs Northwestern UniversityExecutive Director of Administration and Finance, Division of Student AffairsEvanston, IL$185,000–$198,790 / yearThe candidate and their staff will provide financial and human resource guidance and consultation to business managers in Student Affairs departments, performing financial and staffing assessments as directed by the Vice President and Associate Vice President of Operations and Services. Other duties and responsibilities will include: developing long-term cost-effective financing strategies to support unit initiatives; forecasting revenue; determining the fiscal impact of budget allocations; and representing the unit's financial interests to the various internal and external constituent groups.
Associate Director International Regulatory Affairs Advertising & Promotion AbbVie IncAssociate Director International Regulatory Affairs Advertising & PromotionILThis individual is responsible for the implementation of regulatory advertising and promotion strategies for marketed and development compounds in alignment with the overarching global regulatory strategy and global brand plan and leads the international regulatory strategy for the assigned marketed and development compounds. US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html.
Manager Food Safety Quality & Regulatory Affairs (Foreign Material and Operational) Conagra Brands IncManager Food Safety Quality & Regulatory Affairs (Foreign Material and Operational)Chicago, IL$109,000–$159,000 / yearWhen visiting these sites, the physical requirements below may apply: You may be required to walk around the facility, climb stairs/ladders, kneel, or perform repetitive tasks that require hand-eye coordination. We care about your total well-being and will support you with the following, subject to your location and role: Health: Comprehensive healthcare plans, wellness incentive program, mental wellbeing support and fitness reimbursement.
Director Regulatory Affairs Dairy Management Inc.Director Regulatory AffairsRosemont, IL$99,000–$120,000p>The Director will lead day-to-day regulatory affairs activities, working cross-functionally with regulatory, scientific, nutrition and sustainability affairs, marketing and communications, global and domestic partnerships, product research and development and nutrition research teams to ensure that dairy foods are accurately, credibly and compellingly represented in the health and wellness marketplace. National Dairy Council (NDC), the non-profit organization founded by dairy farmers and funded by the national dairy checkoff program, has been committed to research-based nutrition education and communications since its start in 1915.
Director Regulatory Affairs Devices and Combination Products AbbVie IncDirector Regulatory Affairs Devices and Combination ProductsNorth Chicago, ILThe Director Regulatory Affairs, Device is responsible for combining knowledge of scientific, regulatory and business issues to support and drive strategy for regulatory submissions, including new applications and amendments, renewals, annual reports, supplements and variations. Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position.
Associate Director, Regulatory Affairs Baxter International IncAssociate Director, Regulatory AffairsDeerfield, IL$176,000–$242,000 / yearRecruitment Fraud NoticeBaxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. May participate in potential and established third party efforts (i.e. Due diligence activities, joint ventures, etc.).May provide direct supervision of individuals including mentoring, performance management and staffing decisions.
Regulatory Affairs Manager Conagra Brands IncRegulatory Affairs ManagerChicago, IL$107,000–$156,000 / yearYou will work cross‑functionally with functional and operating groups on regulatory topics impacting manufacturing operations, with primary responsibility for regulatory oversight of Conagra factories. When visiting these sites, the physical requirements below may apply: You may be required to walk around the facility, climb stairs/ladders, kneel, or perform repetitive tasks that require hand-eye coordination.
Senior Scientific Director International Medical Affairs - Gastroenterology Cross-IBD Standard of Care Lead AbbVie IncSenior Scientific Director International Medical Affairs - Gastroenterology Cross-IBD Standard of Care LeadILp>The Senior Scientific Director, International Medical Affairs provides specialist medical and scientific input into core strategic and operational medical affairs activities for the International Gastroenterology portfolio such as: health-care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives, scientific communications, value propositioning, and safeguarding patient safety (risk minimization activities and safety surveillance activities). Core Responsibilities: Provides specialist medical insights, and executes on data generation, communication, and expert engagement activities as deliverables to support relevant Asset Strategy Teams (ASTs) for late stage development program including leading or contributing to: comprehensive gap assessment, development of Scientific Communication Platform, development of integrated evidence plans to support launch readiness.
NewSenior Manager - Regulatory Affairs Covista IncSenior Manager - Regulatory AffairsChicago, IL$80,336.75–$145,077.09 / yearp>Under the general direction of the Senior Director of Regulatory Affairs, the Senior Manager, Regulatory Affairs is responsible for ensuring that all Covista advertising, marketing, public- and student-facing communications for all Covista institutions and business units are written in compliance with state and federal regulatory agency requirements. Due to the importance, high visibility of marketing, risks and potential impact related to misrepresentation, the incumbent must have the business acumen to accurately interpret often ambiguous regulations and partner with marketing and operations leaders to accept guidance on marketing practices.
Senior Manager Regulatory Affairs US Advertising and Promotion - US Specialty AbbVie IncSenior Manager Regulatory Affairs US Advertising and Promotion - US SpecialtyILli>Oversees the operations productivity and development of assigned regulatory staff that are responsible for ensuring that advertising and promotion materials are accurate, competitive and compliant with internal policies, Code of Federal Regulations (CFR), FDA guidance documents, PhRMA Guiding Principles, and the Federal Food, Drug, and Cosmetic Act. US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html.
Senior Manager Regulatory Affairs US Advertising and Promotion - Immunology AbbVie IncSenior Manager Regulatory Affairs US Advertising and Promotion - ImmunologyILp>US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html. Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position.
Manager Regulatory Affairs Global Reg Strategy US & Canada AbbVie IncManager Regulatory Affairs Global Reg Strategy US & CanadaNorth Chicago, ILApplicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
NewSenior Manager Regulatory Affairs Global Reg Strategy US & Canada - Immunology AbbVie IncSenior Manager Regulatory Affairs Global Reg Strategy US & Canada - ImmunologyNorth Chicago, ILp>US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html. Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position.
USGlobal Senior Medical DirectorScientific Director Medical Affairs - Multiple Myeloma AbbVie IncUSGlobal Senior Medical DirectorScientific Director Medical Affairs - Multiple MyelomaMettawa, ILProvides scientific and technical support for assigned multiple myeloma products; deliver scientific presentations; develops and maintains professional and credible relationships with, key opinion leaders; actively participate in relevant Brand Teams and helps develop medical affairs strategies for assigned multiple myeloma products; develop innovative research concepts for clinical data generation; provide relevant scientific and technical training. Provides specialist medical/scientific strategic and operational input into core medical affairs activities such as: health-care professional/provider interactions (Payers, Patients, Prescribers, and Providers); generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, data, guidelines and value proposition); safeguarding patient safety (risk minimization activities / safety surveillance activities).
Director, Medical Affairs (Nutrition) Fresenius Kabi AGDirector, Medical Affairs (Nutrition)Lake Zurich, IL$185,000–$220,000 / yearp>The Director, Medical Affairs will lead the field clinical education team and ensure that the respective territory engagement plans are effectively executed per defined targets, following Fresenius Kabi compliance rules and code of conduct and that relevant medical and scientific insight is routinely shared to optimize the Medical Affairs strategy for the nutrition portfolio. 3+ years of hands-on experience in patient care and in hospital and/or clinic and/or home infusion settings is required, with demonstrated expertise in clinical nutrition including experience in managing formula selection for oral nutritional supplement use and tube feeding regimens.
Area TA Lead Director Neuroscience Intercontinental Medical Affairs AbbVie IncArea TA Lead Director Neuroscience Intercontinental Medical AffairsILDevelops and maintains professional and credible relationships with key external experts and professional societies; provides therapeutic expertise in interactions with regulators and other external groups; develops innovative research concepts for clinical data generation and communication. Will work closely with Area commercial teams to provide strategic medical input into core Neuroscience assets strategies, and to support medical/marketing activities and market access; provide scientific and technical support for assigned products.
Associate Director, State Government Affairs - Remote Agios PharmaceuticalsAssociate Director, State Government Affairs - RemoteChicago, ILRemote$153,541–$230,312 / yearThe current base salary range for this position is expected to be between $153,541 and $230,312 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. Our team’s proven track record of executional excellence, combined with our depth of expertise and dedication, enables us to develop innovative medicines that reflect the priorities of rare disease communities.
Director, Medical Affairs (Nutrition) Fresenius KabiDirector, Medical Affairs (Nutrition)Lake Zurich, IllinoisThe Director, Medical Affairs will lead the field clinical education team and ensure that the respective territory engagement plans are effectively executed per defined targets, following Fresenius Kabi compliance rules and code of conduct and that relevant medical and scientific insight is routinely shared to optimize the Medical Affairs strategy for the nutrition portfolio. 3+ years of hands-on experience in patient care and in hospital and/or clinic and/or home infusion settings is required, with demonstrated expertise in clinical nutrition including experience in managing formula selection for oral nutritional supplement use and tube feeding regimens.
NewSenior Analyst - Regulatory Affairs Covista IncSenior Analyst - Regulatory AffairsChicago, IL$49,199.33–$86,253.75 / yearCovista is the parent company of American University of the Caribbean School of Medicine, Chamberlain University, Ross University School of Medicine, Ross University School of Veterinary Medicine and Walden University. Actual pay will be adjusted based on job-related factors permitted by law, such as experience and training; geographic location; licensure and certifications; market factors; departmental budgets; and responsibility.
Senior Director Scientific Affairs Dairy Management Inc.Senior Director Scientific AffairsRosemont, IL$117,000–$135,000p>National Dairy Council® (NDC), the non-profit organization founded by dairy farmers and funded by the national dairy checkoff program, has been committed to research-based nutrition education and communications since its start in 1915. NDC is modernizing its Nutrition, Regulatory, and Sustainability Affairs (NRSA) approach to engage diverse technical audiences that include nutrition scientists/academics, health professionals, and authoritative health and wellness organizations in efforts to educate and amplify the science on the role of dairy foods in health, wellness, and sustainable food systems.
Scientific Director Senior Medical Director Medical Affairs - Parkinsons Disease US AbbVie IncScientific Director Senior Medical Director Medical Affairs - Parkinsons Disease USILActively solicit expert opinion through leader interactions and coordinate scientific and medical activities with internal stakeholders (commercial, market access, HEOR, clinical operations, clinical development, and regulatory) to ensure broad cross-functional perspectives shape Clinical Development Plans and protocols-acting as the scientific team interface for key regulatory discussions. This is a high-impact role for a medically trained scientific leader who takes ownership, exercises independent scientific judgment, and thrives in a fast-paced, evolving environment, navigating ambiguity and competing priorities while driving clarity across matrixed, cross-functional teams.
Scientific Director Senior Medical Director Multiple Myeloma International Medical Affairs AbbVie IncScientific Director Senior Medical Director Multiple Myeloma International Medical AffairsMettawa, ILThe Scientific Director / Senior Medical Director provides specialist medical and scientific input into core strategic and operational medical affairs activities such as: health-care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, scientific communications, and value proposition) and safeguarding patient safety (risk minimization activities and safety surveillance activities). Acts as a clinical interface and actively solicits opinion through leader interactions related to the molecule and disease area; partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are incorporated into Clinical Development Plans and protocols as appropriate.
Scientific Director Medical Director Medical Affairs - Oncology AbbVie IncScientific Director Medical Director Medical Affairs - OncologyILThe Scientific Director / Medical Director provides medical and scientific input into strategic and operational medical affairs activities for AbbVie's Oncology portfolio such as: health-care professional and provider interactions (Payers, Patients, Prescribers, and Providers); generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, data, guidelines, and value proposition); safeguarding patient safety (risk minimization activities and safety surveillance activities). Acts as a clinical interface and actively solicits opinion through leader interactions related to the molecule and disease area; partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are incorporated into Clinical Development Plans and protocols as appropriate.
Scientific Director Medical Director Medical Affairs - Oncology Ovarian Solid Tumor AbbVie IncScientific Director Medical Director Medical Affairs - Oncology Ovarian Solid TumorMettawa, ILThe Scientific / Medical Director, Medical Affairs provides specialist medical and scientific input into core strategic and operational medical affairs activities for AbbVie's Oncology portfolio such as: health-care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives, scientific communications, value propositioning, and safeguarding patient safety (risk minimization activities and safety surveillance activities). The Medical Affairs organization provides patients, healthcare providers, and payers everywhere with the practical and clinically relevant information and solutions they need to use AbbVie products safely and effectively, throughout the product lifecycle and the patient's journey.
Associate Scientific Director Dermatology - US Medical Affairs AbbVie IncAssociate Scientific Director Dermatology - US Medical AffairsILThe Associate Scientific Director, Dermatology - US Medical Affairs provides specialist medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, scientific communications, and value proposition) and safeguarding patient safety (risk minimization activities and safety surveillance activities). Acts as a clinical interface and actively solicits opinion through leader interactions related to the molecule and disease area; partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are incorporated into Clinical Development Plans and protocols as appropriate.
Associate Scientific DirectorScientific Director Dermatology - US Medical Affairs AbbVie IncAssociate Scientific DirectorScientific Director Dermatology - US Medical AffairsILp>The Associate Scientific Director/Scientific Director, Dermatology - US Medical Affairs provides specialist medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, scientific communications, and value proposition) and safeguarding patient safety (risk minimization activities and safety surveillance activities). Acts as a clinical interface and actively solicits opinion through leader interactions related to the molecule and disease area; partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are incorporated into Clinical Development Plans and protocols as appropriate.
Senior Director, Medical Affairs, BDPI – Vascular Platform Becton Dickinson Medical DevicesSenior Director, Medical Affairs, BDPI – Vascular PlatformVernon Hills, IllinoisIn partnership with Medical Safety leadership, oversee medical safety and risk management for the Vascular portfolio, ensuring compliance with global regulatory requirements (e.g., FDA, PMDA, Notified Bodies, GLPs) and providing clinical expertise for adverse event assessment, post‑market surveillance, risk management planning, safety communications, and Field Action Committee activities. Engage early and continuously with cross‑functional partners, including Marketing, Regulatory, R&D, Clinical Affairs, Quality, Business Development, Scientific Affairs, Physician Training, and Global Medical Affairs Regions to align medical strategy with program and platform objectives.
NewScientific Medical Director Global Hematology Pipeline Medical Affairs AbbVie IncScientific Medical Director Global Hematology Pipeline Medical AffairsILThe Scientific/Medical Director, Global Hematology Pipeline, Medical Affairs provides specialist medical and scientific input into core strategic and operational medical affairs activities across the hematology pipeline including disease and asset strategy, scientific differentiation, value propositions, narratives and publication strategy, evidence generation and health-care professional and provider interactions. Acts as a medical interface and actively solicits insights and opinion through the development and execution of medical expert engagement strategies, partnering with clinical development, commercial, access, area and affiliate colleagues to ensure that broad perspectives both internally and externally are incorporated into strategies and plans as appropriate.
Senior Director, Medical Affairs, BDPI - Vascular Platform Becton Dickinson and CoSenior Director, Medical Affairs, BDPI - Vascular PlatformIL$181,400–$326,500 / yearli>In partnership with Medical Safety leadership, oversee medical safety and risk management for the Vascular portfolio, ensuring compliance with global regulatory requirements (e.g., FDA, PMDA, Notified Bodies, GLPs) and providing clinical expertise for adverse event assessment, post‑market surveillance, risk management planning, safety communications, and Field Action Committee activities. Engage early and continuously with cross‑functional partners, including Marketing, Regulatory, R&D, Clinical Affairs, Quality, Business Development, Scientific Affairs, Physician Training, and Global Medical Affairs Regions to align medical strategy with program and platform objectives.
Director, State Government Relations & Public Affairs Covista IncDirector, State Government Relations & Public AffairsChicago, IL$100,171.61–$181,034.70 / yearYou"ll be expected to anticipate and navigate fast-paced news, legislative and regulatory environment, build the political conditions for Covista"s strategic priorities before they"re at risk, and serve as a proactive counselor to institutional and segment leaders and other internal stakeholders needing to navigate state- and local-level decisions. Covista is the parent company of American University of the Caribbean School of Medicine, Chamberlain University, Ross University School of Medicine, Ross University School of Veterinary Medicine and Walden University.
Director Oncology Public Affairs AbbVie IncDirector Oncology Public AffairsILStrong communication planning, execution and process management skills and strong interpersonal skills to quickly build rapport and credibility with AbbVie leaders as well as key internal and external stakeholders, including academic experts, patients and patient advocates, with confidence, empathy and ease. Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position.
NewMedical Affairs Scientific Communications Director - Movement Disorders H. Lundbeck ASMedical Affairs Scientific Communications Director - Movement DisordersDeerfield, ILRemoteThis individual will partner closely with HEOR, Commercial, Customer insights & analytics, Patient advocacy, Clinical Development, Compliance, Legal, Medical Affairs Operations, and Medical Affairs teams and external experts to ensure scientific materials are accurate, balanced, compliant, and aligned with medical objectives while serving as a scientific communications expert across the organization. SUMMARY: The Medical Affairs Scientific Communications Director will lead the strategic development and execution of scientific communication plans for MSA that support launch readiness and are aligned with the needs of patients, caregivers, healthcare professionals, payers, and policymakers.
Associate Director, State Government Affairs Financial Industry Regulatory Authority IncAssociate Director, State Government AffairsChicago, ILFINRA employees are required to disclose to FINRA all brokerage accounts that they maintain, and those in which they control trading or have a financial interest (including any trust account of which they are a trustee or beneficiary and all accounts of a spouse, domestic partner or minor child who lives with the employee) and to authorize their broker-dealers to provide FINRA with duplicate statements for all of those accounts. Additional insurance includes basic life, accidental death and dismemberment, supplemental life, spouse/domestic partner and dependent life, and spouse/domestic partner and dependent accidental death and dismemberment, short- and long-term disability, long-term care, business travel accident, disability and legal.
Assistant Principal of Academic Affairs Illinois Association of School AdministratorsAssistant Principal of Academic AffairsIL$82,000–$95,000 / yearUrl&choosedistricttrue&applitrackclient207&categoryAdministrationILearn LinkILearnReport Card LinkDistrict Report Card Job Posting Date 182026 Start Date 812026 SharePrint«Back to Search Results Job DetailsDistrict Name Plano Comm 88Building Name Plano High SchoolAddress 704 W. Job Details | IASA Job BankToggle NavigationHome Sign In or RegisterSearch for OpeningsWelcome to the Illinois Education Job Bank where you can Search Openings Save Resumes and Apply Online for FREEJob DetailsAssistant Principal of Academic AffairsSharePrintDutiesPERFORMANCE RESPONSIBILITIES1.
SVP, Head of Government Affairs and Public Policy Safelite Group, Inc.SVP, Head of Government Affairs and Public PolicyChicago, ILThis role provides executive leadership across lobbying, policy research and analysis, advocacy, political engagement, and regulatory strategy, while building and sustaining trusted relationships with policymakers, regulators, industry associations, OEMs, clients, and internal stakeholders. The SVP, Head of Government Affairs and Public Policy serves as Safelite's most senior government affairs and public policy leader, responsible for developing and executing a comprehensive strategy to shape public policy, influence legislative and regulatory outcomes, and advance the company's business objectives at the federal, state, and local levels.
Director Global Environmental Affairs Ingredion IncDirector Global Environmental AffairsWestchester, IL$181,400–$241,866.67 / yearCommunicate significant risk issues to the Operations Leadership Team (OLT) and senior leaders with respect to environmental incidents and reporting, root-cause assessments, corrective actions, and non-compliances to drive change and improvements from the top down. Oversees consulting partners to complete an evaluation of potential EHS&S and engineering risks with respect to site contamination, non-compliance, safety risks (e.g., combustible dust/explosion prevention, electrical safety, etc.), and the ability to expand operations to meet business objectives.
Regional Environmental Affairs Director Reworld Holding CorpRegional Environmental Affairs DirectorChicago, IL$157,000–$224,400 / yearAll Reworld positions require a candidate's ability to perform the duties and responsibilities of the role while upholding Reworld's Values, including (but not limited to) contributing to a safe and inclusive workplace, delivering results through trust, and building breakthrough capabilities. The successful candidate must have 10+ years of progressively responsible experience in diverse environmental areas including compliance, permitting, stack tests, sustainability, climate change, etc., and be located in the Chicago area (or willing to relocate).
Regulatory Affairs Manager Hollister IncRegulatory Affairs ManagerLibertyville, IL$130,000–$185,000 / yearHollister is a wholly owned subsidiary of The Firm of John Dickinson Schneider, Inc., and is guided both by its Mission to make life more rewarding and dignified for people who use our products and services, as well as its Vision to grow and prosper as an independent, employee-owned company, and in the process, to become better human beings. The Company's health and welfare benefits include medical, prescription, dental, vision, spending/savings accounts, disability, company paid (parental and caregiver) leaves, statutory leaves/disability programs, accident, life, wellbeing, education assistance, adoption assistance, and voluntary benefit programs.
Sr. Scientific and Regulatory Affairs Manager -Packaging Sustainability Mars IncSr. Scientific and Regulatory Affairs Manager -Packaging SustainabilityChicago, ILThe position drives proactive horizon scanning, regulatory intelligence, and risk assessment for emerging materials and regulatory trends, develops internal tools, systems, and governance frameworks, and delivers pragmatic solutions including technical arguments, exemptions, and advocacy with trade associations and regulatory agencies. Scientific and Regulatory Affairs Manager - Packaging Sustainability leads Mars Snacking North America efforts to interpret, apply, and influence complex and evolving sustainability regulations, translating legislation on packaging design, labeling, claims, and chemicals of interest into clear technical requirements and internal specifications.
Director of Regulatory Zebra Technologies CorpDirector of RegulatoryLincolnshire, IL$177,920–$266,880 / yearEffectively communicate regulatory matters, providing clear, strategic guidance to key stakeholders, including senior and executive leadership to guide critical business decisions and long-range planning. As the companys spokesperson on regulatory matters, this is a highly visible role that requires building strategic partnership across the business and evolving the regulatory function into a competitive advantage.
Regulatory Affairs Manager, Research Incubation Unit University of ChicagoRegulatory Affairs Manager, Research Incubation UnitHyde Park, IL$65,000–$90,000 / yearThe Clinical Research Incubation Unit was established to enable growth of clinical research portfolios across the Biological Sciences Division as well as provide timely research staffing services to departments or units in need of short-term clinical research management services. The mission of the Office of Clinical Research is to catalyze clinical research by providing expertise, resources, infrastructure, and systems that facilitate clinical research operations and enable collaboration across the enterprise while promoting compliance and human subject protection on behalf of our diverse community of patients and volunteers.
Regulatory Affairs Manager Katalyst Healthcares & Life SciencesRegulatory Affairs Managermossville, ILResponsibilities: Lead regulatory strategy and submissions for Class II and III medical devices in the U.S. Prepare and manage regulatory submissions including 510(k), PMA Supplements, annual reports. We are seeking a highly experienced and motivated Manager, Regulatory Affairs, to join our growing Regulatory Affairs team.
Regulatory Affairs Senior Manager Bel SARegulatory Affairs Senior ManagerChicago, IL$145,000–$150,000 / yearp>As the Senior Manager Regulatory Affairs for Bel US, you will lead regulatory affairs for Bels cheese brands, overseeing complex projects and representing the company externally within the dairy industry. Drive continuous improvement in internal policies, processes, and ways of working to enhance regulatory efficiency and effectiveness, working collaboratively as one team with other North American and global regulatory team members.
NewSr. Regulatory Affairs Manager RoquetteSr. Regulatory Affairs ManagerGeneva, IllinoisOrganize and lead development of regulatory dossiers to support new products and expanded uses across food ingredients, industrial applications, animal feed, and plant care. Partner with Quality Assurance to support quality systems, including change controls, raw material and processing aid evaluations, and process improvements.