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.
NewSr Mgr, Regulatory Affairs Baxter International IncSr Mgr, Regulatory AffairsDeerfield, IL$152,000–$209,000 / yearYour role at BaxterA Senior Manager of Global Regulatory Affairs leads the development and execution of regulatory strategies to support product approvals, lifecycle management, and compliance across international markets, with deep expertise in US FDA requirements. Recruitment 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.
Manager Regulatory Trade Compliance Medline Industries LPManager Regulatory Trade ComplianceIL$116,000–$174,000 / yearThis role serves as the primary bridge between Regulatory Affairs, Imports/Logistics, Legal, and Corporate Compliance to ensure that FDA import data and processes are accurate, consistent, and aligned across all internal systems, contract manufacturers, suppliers, and customs brokers. Oversee and validate FDA entry data elements including FDA Product Codes, Intended Use Codes, Affirmations of Compliance (AofC), Establishment Registration Numbers, Medical Device Listing (MDL) numbers, Manufacturer and importer identifiers.
NewRegulatory Affairs Specialist, Cosmetics and OTC Personal Care, Growing Contract Manufacturer Pave TalentRegulatory Affairs Specialist, Cosmetics and OTC Personal Care, Growing Contract ManufacturerOttawa, Illinois2 to 4 years of Regulatory Affairs experience within cosmetics, personal care, or OTC manufacturing — beauty industry backgrounds strongly preferred; pharma-only or food backgrounds will not be considered. You will report to the Global Manager of Regulatory Affairs and serve as that person's key specialist, supporting compliance across a broad portfolio of cosmetic, personal care, and OTC drug products.
Senior Manager Regulatory Strategy H. Lundbeck ASSenior Manager Regulatory StrategyDeerfield, ILRemoteli>Manages the processing of regulatory submissions with Strategy leadership and operational support; ensures submissions are prepared in compliance with regulatory requirements and guidance documents; ensures that appropriate review and approval is obtained. Working with US regulatory management and the Global Regulatory Lead, serves as US subject matter expert to support strategy development and execution for assigned products.
Regulatory Affairs Specialist III - Diabetes Care (on-site) Abbott LaboratoriesRegulatory Affairs Specialist III - Diabetes Care (on-site)Buffalo Grove, IL$68,000–$136,000 / yearli>Provides support to Regulatory Affairs management when working towards resolution of compliance issues assuring these resolutions comply with site and division level policies and procedures and are aligned with the appropriate quality system. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.
Regulatory Affairs Specialist III – Diabetes Care (on-site) AbbottRegulatory Affairs Specialist III – Diabetes Care (on-site)Buffalo Grove, Illinoisli>Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree. Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.
Sr Spec Regulatory Affairs Medline Industries LPSr Spec Regulatory AffairsIL$92,000–$138,000 / yearComplete 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 Industries LPSr. Regulatory Affairs SpecialistIL$92,000–$138,000 / yearComplete 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.
Senior Regulatory Affairs Specialist Medline Industries LPSenior Regulatory Affairs SpecialistIL$92,000–$138,000 / yearComplete 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.
Senior Manager, Food Safety & Quality Compliance TreeHouse Foods IncSenior Manager, Food Safety & Quality ComplianceOak Brook, IL$124,800–$187,200 / yearAn employee's position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, seniority, geographic location, performance, shift, travel requirements, sales or revenue-based metrics and business or organizational needs. Provide technical guidance to facility and warehouse personnel in developing systems, knowledge, and practices to ensure compliance with food safety regulations, company policies, and external audits (including customer, certification, GFSI, and regulatory).
Quality Compliance Lab Manager Sterling Engineering, Inc.Quality Compliance Lab ManagerBuffalo Grove, ILPosition SummaryThe Quality Compliance Lab Manager is responsible for leading a regulated laboratory environment supporting medical device testing, with a strong focus on blood-based assays for product performance, accuracy, and quality control. The manager provides both technical and people leadership, ensuring the laboratory operates efficiently, remains inspection-ready, and delivers reliable analytical results that support product quality and patient safety.
NewDirector US Regulatory Global Strategic Labelling H. Lundbeck ASDirector US Regulatory Global Strategic LabellingDeerfield, ILRemoteli>Partners with cross functional teams providing labeling expertise and regulatory knowledge to author and develop competitive and optimal target product labelling (TPL), CCDS, EU SmPC, USPI, CPM, Carton and Container and other labelling materials required for marketing registration that aligns with Organizational business strategy and regulatory requirements. Provides competitive labeling intelligence and insights to communicate initial labeling frameworks and regulatory expertise to address labeling challenges during development and post-approval maintenance of global labelling activities, ensuring cross functional communication and execution per process.
Regulatory Advisor Livingston International Inc.Regulatory AdvisorSchaumburg, ILRespond and assist internal and external clients with their inquiries or requests; troubleshoot and resolve client's issues in a timely manner and escalate complex issues or inquiries to the Manager, US Regulatory Affairs. Build and maintain close relationships with government agencies, departments and associations to obtain information and insight to pending legislation and operational process changes.
Product Development Manager - Dog & Cat Regulated Products Central Garden & PetProduct Development Manager - Dog & Cat Regulated ProductsSchaumburg, IL$110,000–$140,000 / yearFull timeIf you are ready to take the next exciting step in your research and development career, we’d love to hear from you! Please see our website for additional company information – www.central.com KEY RESPONSIBILITIES Lead the development of new Pet Health & Wellness products from concept through commercialization, partnering with cross-functional teams including R&D, Regulatory, Quality, Marketing, Legal, Procurement, and Manufacturing. Provide technical support to Consumer Care by assisting with responses to customer inquiries related to product efficacy, usage, and concerns; develop accurate, science-based guidance and leverage consumer feedback to inform continuous improvement, quality enhancements, and future product innovation.
Director US Regulatory Strategy H. Lundbeck ASDirector US Regulatory StrategyDeerfield, ILRemoteThe Director, US Regulatory Affairs Strategy, oversees the implementation of regulatory strategies to ensure the successful development and approval of assigned drug and biological products for the United States (global products as well as US only products). Through cutting edge science and strong partnerships, we develop and market some of the world's leading treatments, expanding into neuro-specialty and neuro-rare from our strong legacy within psychiatry and neurology.
Software Project Manager (Glenview, IL) GN Store Nord ASSoftware Project Manager (Glenview, IL)Glenview, ILWe don't just run projects - we continuously reinvent how we work, improving processes, modernizing ways of working, and exploring how AI can enable smarter delivery and better outcomes. Own projects and collaborate closely with product owners, product managers, commercial teams, hardware/embedded software specialists, and regulatory affairs.
NewRegulatory Affairs Specialist DEL MEDICAL IncRegulatory Affairs SpecialistBloomingdale, ILManage the overall development and approval process for assigned documents (CEP, CER, etc.) within timelines, including documentation generation, initiation of the review process, discussions on proposed revisions, and document completion in collaboration with other team members. You will work cross-functionally with Engineering, Quality, Manufacturing, and Leadership teams to ensure our products meet all applicable regulatory requirements throughout the product lifecycle.
Quality Assurance Manager MRINetwork JobsQuality Assurance ManagerItasca, IllinoisThe Quality Manager is responsible for leading the Quality Assurance function and overseeing the Quality Management System (QMS) to ensure that all medical devices comply with FDA 21 CFR Part 820, ISO 13485, ISO 14971, and other applicable global regulatory requirements. Participate in post-market surveillance activities, including complaint handling, MDRs/adverse event reporting, trend analysis, and implementation of corrective actions.
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.
NewPublic Affairs Lead, Americas Industrial and Financial Systems ABPublic Affairs Lead, AmericasIL$135,000–$150,000 / yearReporting to the Head of External Affairs, you''ll be responsible for monitoring policy developments, engaging with federal and state government stakeholders, managing relationships with premier institutions like the World Economic Forum and Milken Institute, and positioning IFS as a credible, influential voice in technology policy debates. You''ll operate at the intersection of technology, policy, and global affairs-building coalitions, shaping positions, and ensuring IFS stays ahead of regulatory and legislative developments that impact our business.
Engineer, Principal Regulatory Constellation Energy Generation, LLC.Engineer, Principal RegulatoryWarrenville, IllinoisUnderstands interrelations and functions of various organizations (e.g., Nuclear Regulatory Commission (NRC), Institute of Nuclear Power Operators (INPO), Nuclear Energy Institute (NEI), North American Electric Reliability Corporation (NERC) etc.) related to nuclear power. Perform independent and in-depth research, reviews, studies and analyses to develop, manage and implement regulatory activities, related to plant safety, reliability, maintainability, and availability ensuring compliance to site's needs, regulatory requirements, and corporate policies.
Senior Regulatory Affairs Specialist Abbott LaboratoriesSenior Regulatory Affairs SpecialistIL$78,000–$156,000 / yearOur portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. The crucial information derived from our tests, instruments and informatics systems are often the first step in patient care decision making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers.
Manager Market Strategy & Analysis CalpineManager Market Strategy & AnalysisDowners Grove, IllinoisThe primary focus of the position is retail electric markets in the Northeast and Midwest U.S. The candidate will support Calpine Retail supply, commercial and sales teams by (1) monitoring, analyzing and communicating key regulatory policy developments that may directly or indirectly impact the company and (2) advocating policies that enhance Calpine’s business processes. Support Calpine Retail commercial, supply and sales efforts by monitoring market developments and performing comprehensive analysis of proposed/existing regulations and legislation; includes identifying, quantifying and communicating the impact of potential policy changes.
Regulatory Affairs Specialist Actalent IncRegulatory Affairs SpecialistDes Plaines, IL$38–$43 / hourIn this role, you won't just maintain compliance-you'll drive registrations, build and manage dossiers, interface with agencies, and influence regulatory strategy across products that support animal health, food safety, and global dairy production. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
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.
Sr. Design Quality Engineer Avalign Technologies IncSr. Design Quality EngineerSchaumburg, ILli>Supports, reviews, and approves the following activities associated with new product development: identification and documentation of user needs, design inputs, outputs, verification, validation, risk assessment, and design change activities to demonstrate new product designs are supported by objective evidence in the design history file prior to product launch. (ISO 13485, ISO 14971, 21 CFR Part 820, and, preferably, EU Medical Device Regulation) The position requires a hands-on self-directed style, and the ability to influence and effectively communicate vertically, horizontally, across functions, externally with customers and internally with co-workers.
Managed Services Sr. Consultant Deloitte Touche Tohmatsu LtdManaged Services Sr. ConsultantIL$120,200–$140,000 / yearLead and contribute to end-to-end delivery for Generis CARA and associated regulatory technology platforms - including requirements gathering, solution design, system configuration, content template development, and user acceptance testing. Our purpose comes through in our work with clients that enables impact and value in their organizations, as well as through our own investments, commitments, and actions across areas that help drive positive outcomes for our communities.
Team Lead RAPV Data Governance and Compliance Astellas Pharma IncTeam Lead RAPV Data Governance and ComplianceNorthbrook, ILContributes to and executes against the RAPV strategy by creating 1-3 year plans for the RA system and process capabilities, aligning their group with the other RAPV Enablement groups, considering industry initiatives, Health Authority guidances, software vendor capabilities, corporate strategy, internal RA process improvements, system interactions with other functions and end user input. Identifies the need for and ensures the assimilation of detailed interpretive analyses of complex regulatory guidance documents, regulations, or directives that impact products and operations; prioritizes short- and long-term projects to implement relevant changes in system configurations and business processes to maximize efficiency and/or improve compliance.
Principal Scientist Fresenius Kabi AGPrincipal ScientistMelrose Park, IL$80,000–$95,000 / yearBachelor's degree in, Chemistry, Pharmaceutical Sciences Biological Sciences with seven plus years of related experience or a Master's Degree in Pharmaceutical Sciences, Chemistry, Biological Sciences with 5 years of related experience or a PhD in Chemistry, Pharmaceutical Sciences, Biological Sciences, Chemical/Biomedical Engineering with one to three years of related experience is required. Prepare and review regulatory affairs (RA) documentation for Extractables & Leachables (E&L) studies, ensuring alignment with global regulatory requirements, and effectively respond to FDA queries with clear, scientifically sound justifications supported by robust data and technical expertise.
Principal Scientist Fresenius KabiPrincipal ScientistMelrose Park, IllinoisBachelor’s degree in, Chemistry, Pharmaceutical Sciences Biological Sciences with seven plus years of related experience or a Master’s Degree in Pharmaceutical Sciences, Chemistry, Biological Sciences with 5 years of related experience or a PhD in Chemistry, Pharmaceutical Sciences, Biological Sciences, Chemical/Biomedical Engineering with one to three years of related experience is required. Prepare and review regulatory affairs (RA) documentation for Extractables & Leachables (E&L) studies, ensuring alignment with global regulatory requirements, and effectively respond to FDA queries with clear, scientifically sound justifications supported by robust data and technical expertise.
Regulatory Coordinator Actalent IncRegulatory CoordinatorNorthbrook, IL$24–$28.85 / hourThis position manages key regulatory processes, maintains essential documentation, and partners closely with functions such as Legal, Sales, Marketing, and R&D to enable safe, compliant, and successful product launches in the flavor and fragrance industry. The Regulatory Coordinator plays a critical role in ensuring that products comply with local, national, and international regulations while providing high-quality support to internal teams and external customers.
NewSr. Corporate Counsel - Corp Governance Zurich Insurance Group LtdSr. Corporate Counsel - Corp GovernanceSchaumburg, ILProvide a full range of legal advice and services on corporate legal issues relevant to objectives set by the Corporate Legal Team Lead/General Counsel which may include concerning Governance, Communications, Investor Relation, Regulatory Affairs, Finance and Capital Market transactions, Sourcing, IT, Data Protection. In this role you will be responsible to: Identify, manage and mitigate legal, regulatory and corporate governance risks, to enable the business to achieve its strategic and commercial goals in accordance with applicable laws and regulations and to protect and preserve Zurich's tangible and intangible assets.
Sr. Regulatory Analyst Southern CoSr. Regulatory AnalystNaperville, ILThe company has electric operating companies in three states, natural gas distribution companies in four states, a competitive generation company, a leading distributed energy solutions provider with national capabilities, a fiber optics network and telecommunications services. The role partners closely with the Regulatory Affairs team to manage Illinois Commerce Commission (ICC) proceedings, workshops, and filings, requiring strong analytical capabilities and cross-functional coordination.