89 Results for

Regulatory Affairs Jobs in Schiller Park, IL

Jobs

New!

Deerfield, IL5 days ago

Remote

$175,000–$205,000

The Associate Director, Regulatory Strategy provides key support to the Regulatory Affairs team and pipeline programs supporting the creation and implementation of regulatory strategies to ensure the successful US development and approval of assigned drug and biological products (developmental and marketed products). 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.

Deerfield, IL11 days ago

Remote

$200,000–$235,000

The 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). Serves as primary regulatory contact for alliance product brands, as assigned, including managing cross-functional and multi-leveled governance and alignment meetings.

Warrenville, IL11 days ago

$152,100–$169,000

Understands 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.

Chicago, IL11 days ago

Knowledge and understanding of FDA product codes and product class structure, Quality Management Systems and Good Manufacturing Practices, or willingness to learn through training and independent research. - Train and mentor new employees, divisional QA's and product managers on regulatory product structure, regulatory labeling requirements, and Medline labeling procedure(s).

New!

Deerfield, IL5 days ago

Remote

$225,000–$265,000

They will be charged with building a multifaceted plan in alignment with company milestones and develop programs and initiatives that drive disease awareness, support launch readiness and commercialization success, and collaborate with advocacy groups to cocreate resources and initiatives that empower patients and caregivers. Implement strategies to drive early treatment urgency, disease awareness, support important regulatory and commercial milestones, and build an integrated advocacy plan in alignment with Corporate Affairs, Medical, HEOR, Patient Services, and Market Access.

New!

Mundelein, IL5 days ago

Typically requires a Bachelor’s degree in a relevant field AND 1+ year of experience in complaint handling, MDR evaluation, post‑market surveillance, regulatory affairs, or other relevant experience within a regulated industry. Evaluate new and historical complaint files to determine MDR reportability under 21 CFR 803, applying current criteria, definitions, and decision logic to reach a regulatory reporting decision.

New!

Mundelein, IL4 days ago

Evaluate new and historical complaint files to determine MDR reportability under 21 CFR 803, applying current criteria, definitions, and decision logic to reach a regulatory reporting decision. Work cross‑functionally with Quality, Regulatory Affairs, R&D, Operations, and other internal partners to gather missing complaint or product information required for accurate reportability assessments.

New!

Winnetka, IL2 days ago

Remote

Must be team oriented, with the ability to work well on common deliverables with diverse cross-functional teams and to interact at the highest professional manner with excellent communication skills, both verbal and written, and interpersonal skills to successfully partner on varying levels ranging from cross functional to global multi-site. This position ensures product safety and leads risk mitigation efforts in the form of biological evaluations, chemical characterization, and toxicological risk assessments for medical devices, OTC, and cosmetic products.

Aurora, Illinois8 days ago

This combination of skill and knowledge results in improved patient outcomes, higher quality services and reduced cost of care for hospitals, blood centers, hospital systems, research and educational institutions, and other health care providers. Position Summary: This role provides advanced support to the Quality department in the area(s) of regulatory affairs and acts as a senior member of the Quality team to meet the goals and objectives of the department and potentially other service lines.

North Chicago, IL26 days ago

$158.10–$168.25 Per Hour
Temporary
Contractor
Full-time

Responsibilities :Under appropriate supervision, manages the design, implementation, and evaluation of clinical study protocols in support of the clinical development program and aligned with the overall Product Development Plan, applying sound medical and scientific judgment, knowledge of compliance and regulatory requirements, and awareness of Client’s customers, markets, business operations, and emerging issues. Contributes to training and knowledge sharing within the Clinical Development team, including procedures, clinical monitoring practices, data quality, actionable data interpretation, and workflow integration, as appropriate.

Rosemont, IL30+ days ago

Contractor

Partner with Regulatory Affairs, Quality Assurance, Marketing, and Product Development teams to compile required information and ensure compliance for all new products, changes to existing products, and post-market activities related to drug-device combination products. The Regulatory Affairs Specialist/Senior Specialist for Drug-Device Combination Products will serve as an essential resource within the organization, providing technical expertise and regulatory guidance for the development, manufacturing, and commercialization of drug-device combination products.

Rosemont, IL30+ days ago

$99,000–$120,000

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. Additionally, the Director will support DMI’s engagement with the broader regulatory community by monitoring policy developments, contributing technical expertise to industry discussions and collaborating with leading organizations to help ensure dairy is appropriately represented within evolving food and nutrition and regulatory frameworks.

Chicago, IL30+ days ago

$161,400–$300,700 Per Year

The H&W portfolio includes microbiome solutions and specialty health products and ingredients such as prebiotic dietary fibers, plant- and nutritional oils, mixed tocopherols and vitamin E, sterols, sterol esters, isoflavones, natural preservation systems, etc. We are committed to attracting and retaining a diverse workforce and create welcoming, truly inclusive work environments — environments that enable every ADM colleague to feel comfortable on the job, make meaningful contributions to our success, and grow their career.

North Chicago, IL30+ days ago

$121,000–$230,000 Per Year

236:2002, ANVISA RDC No. 16, JPAL Ordinance 169, MFDS No. 219, ISO 14155, eCTD Module 3, ISO/IEC 62366, HE 74, device complaint handling/MDRs, human factors testing, device risk analysis (ISO 14971) and other global regulatory requirements for Allergan’s devices and combination products. + Represents RA Device on teams such as the product development, Global Regulatory Product Teams, and Operations brand teams, for assigned projects; negotiates with and influences team members with support of management to maximize chances for first pass approval of regulatory submissions.

Chicago, IL30+ days ago

Remote

$183,549–$275,324 Per Year

The current base salary range for this position is expected to be between $183,549 – $275,324 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. As a key cross-functional partner, the Medical Director collaborates closely with Commercial, Clinical Development, Regulatory, and Market Access teams, among others, to shape brand and portfolio strategy, integrating real-world evidence and external expert perspectives.

Mettawa, IL30+ days ago

$129,500–$219,000 Per Year

_Come explore opportunities within Brunswick, a global marine leader (https://youtube.com/watch?v=ksuQ6B2j_mA) committed to challenging conventions and innovating next-generation technologies that transform experiences on the water and beyond. + Federal, State & Local Engagement: Direct advocacy efforts across all levels of government, with a focus on building bipartisan relationships and shaping public policy in areas such as environmental sustainability, workforce development, and innovation.

Aurora, IL15 days ago

The Senior Manager will shape legislative, regulatory, and facilitate community outcomes that support power availability, project delivery, sustainability goals, and long term operational certainty in a rapidly evolving digital infrastructure landscape driven by cloud and AI demand. CyrusOne’s leading global platform of hybrid-cloud and multi-cloud deployments offers customers colocation, hyperscale, and build-to-suit environments, which help enhance the strategic connections of their essential data infrastructures and support the achievement of sustainability goals.

Evanston, Illinois30+ days ago

$165,000–$190,000 Per Year

Responsibilities: The Regional Vice President of Communications and External Affairs is a corporate and regional executive leader responsible for the planning, development and execution of the organization's strategic communications and public relations to advance the mission and organizational goals through effective messaging, media relations, crisis communication, employee engagement, advocacy, and stakeholder outreach. Experience and knowledge in effectively leading and executing corporate and regional-level communications, executive communications, crisis communications, media relations and public relations, as well as labor related communications.

Glenwood, IL22 days ago

$88,000–$147,000 Per Year

Execute New Product Introduction (FAI)/Design Transfer activities in characterizing manufacturing processes for parts/components in development to ensure smooth transition from Research & Development to manufacturing, including participation and leadership of the development of equipment and process validation requirements (Failure Modes and Effects Analysis, Installation Qualification, Operational Qualification, Performance Qualification), using appropriate statistical tools and techniques. + Spend time on the manufacturing floor to determine process improvements, participating in investigations, root cause analyses, corrective action planning, implementation activities and interfacing with all cross functional departments to increase product quality using recognized Six Sigma and Lean methodologies.

Warrenville, Illinois30+ days ago

Chicago, IL30+ days ago

$25.20–$35.60 Per Hour

Relevant certification as a Certified Clinical Research Professionals (CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified IRB Professional (CIP) strongly preferred or required within 1 year of employment. This positions provides regulatory support for multiple clinical research studies, which may involve multi-centered cooperative group studies, single site studies, intergroup studies, industry studies, and investigator initiated studies.

Bedford Park, IL17 days ago

$70,000–$95,000 Per Year

The ideal candidate works comfortably across functions, navigates complex regulatory issues with confidence, and helps deliver practical risk‑aware solutions while managing multiple priorities in a fast-paced, regulated environment both independently and in team settings. Act as a trusted compliance advisor across the organization to promote awareness of regulatory requirements, audit findings, and compliance expectations across the organization through the development, implementation, and maintenance of compliance policies, procedures, and controls related to personal & commercial auto insurance and general liability insurance.

Chicago, Illinois30+ days ago

$88,000–$118,000 Per Year

Wipfli LLP is a licensed independent CPA firm that provides attest services to its clients, and Wipfli Advisory LLC provides tax and business consulting services to its clients. Provide pro-active and on-going consultation regarding regulatory compliance risk assessment, remediation, monitoring, research, interpretation, change management, education, and board and management reporting.

Chicago, Illinois18 days ago

Baker Tilly Advisory Group, LP and Baker Tilly US, LLP, trading as Baker Tilly, are independent members of Baker Tilly International, a worldwide network of independent accounting and business advisory firms in 141 territories, with 43,000 professionals and a combined worldwide revenue of $5.2 billion. Baker Tilly is a leading advisory, tax and assurance firm, providing clients with a genuine coast-to-coast and global advantage in major regions of the U.S. and in many of the world's leading financial centers - New York, London, San Francisco, Los Angeles, Chicago and Boston.

Downers Grove, Illinois22 days ago

You will serve as a trusted legal partner to executive leadership and operational teams—supporting ARCO’s government projects, protecting company data and systems, and ensuring compliance across an expanding regulatory landscape. This role requires someone who can translate complex regulatory frameworks into clear, actionable guidance for project teams while helping build a scalable compliance function across the organization.

Bedford Park, IL9 days ago

$70,000–$95,000 Per Year

Hoffman Estates, Illinois30+ days ago

$100,000–$160,000 Per Year

This role ensures that products perform exactly as claimed and meet all regulatory requirements prior to release. Preparing FCC filings, test reports, and certification documentation.

Buffalo Grove, IL20 days ago

Position 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.

Chicago, IL30+ days ago

Remote

$229,562–$344,342 Per Year

The role oversees a high-impact team and partners cross-functionally and externally to drive an integrated publications and scientific communications strategy, translating complex data into compelling evidence that supports clinical adoption, informs healthcare decision-making, and differentiates the company’s portfolio globally. Agios Pharmaceuticals is searching for a dynamic Senior Director, Global Scientific Communications and Publications expert to join our Global Medical Affairs team and lead a high-functioning communications/publications/congress team.

Itasca, Illinois29 days ago

$180,000–$205,000 Per Year

Overview: Ajinomoto Health & Nutrition North America is seeking a highly strategic and commercially driven Associate Director, Product Management – Animal Nutrition to lead growth initiatives within the AjiPro® portfolio, including rumen-protected amino acids and livestock nutrition solutions. This position is ideal for a senior-level professional with strong experience in animal nutrition, feed additives, amino acids, ruminant nutrition, livestock production, and product commercialization, combined with the ability to drive strategic growth in complex global organizations.

Chicago, IL15 days ago

Full-time
Employee

As an Associate Product Counsel on the Payments product counseling team, supporting engineering, product management, and product strategy in navigating legal issues related to payments, data protection, and new innovative features. Collaborate closely with engineering, product management, and product strategy to develop strategic, practical, and creative solutions to achieve business goals while mitigating legal risks for the Payments product area and Google as a whole.

Chicago, IL30+ days ago

$187,616–$307,008 Per Year

Provide legal advice and counsel to business leadership on a wide range of health law, regulatory, contractual, and operational matters impacting Carelon Services businesses, including behavioral health, medical benefits utilization management, specialty care solutions, and care delivery companies. + Collaborate with internal subject matter experts within Elevance’s larger Legal, Compliance, and Public Affairs functions to provide comprehensive support and clear, consolidated legal advice to the Carelon Services businesses.

Glenwood, IL29 days ago

$70,600–$117,900 Per Year

The Document Control Specialist will be responsible for managing document workflows, ensuring proper configuration control, supporting audits, maintaining training and quality records, and partnering with cross‑functional teams to uphold documentation accuracy, accessibility, and regulatory compliance. We're a force for progress, working alongside our customers and partners to solve challenges on a global scale, from workplace safety in the most demanding conditions to advanced technologies that help providers focus on exceptional patient care.

Rosemont, IL30+ days ago

$120,000–$155,000 Per Year

As a trusted partner, we provide actionable solutions and innovation through our Aerospace Technologies, Building Automation, Energy and Sustainability Solutions, and Industrial Automation business segments – powered by our Honeywell Forge software – that help make the world smarter, safer and more sustainable. The Lead Product Stewardship provides expert product stewardship guidance and leadership to the business and technology developers regarding compliance with North and South American chemical regulations in the areas of existing and new chemicals registration and product safety.

Chicago, Illinois30+ days ago

$120,000–$175,000 Per Year

Grant formal approval via signature authority for the cross-functional promotional review activities including: 1) providing strategic scientific consultations on brand messages, 2) reviewing promotional materials for content and accuracy, 3) coordinating the development, review, and approval of clinical data on file to support promotional claims. This individual’s primary responsibilities are to provide advanced medical and scientific review of: 1) promotional materials, press releases, and sales training communications to support the promotional review process, 2) medical and scientific medical materials, and 3) other pertinent publications in the therapeutic areas, and serve as a resource to other colleagues as needed.

Chicago, Illinois20 days ago

The QISG team brings together Engineering, Safety, Quality, Material Procurement, QA/QC, Right-of-Way Acquisition, Scheduling, Environmental Planning, Permitting, Title and Land Management expertise that ensure outstanding results for our clients. What You'll Bring: Minimum of 15 years’ experience in the electric utility industry performing engineering related duties and/or management for high voltage electrical projects.

Vernon Hills, IL30+ days ago

Full-time

Supervises, directs, and motivates community management while empowering department leaders to supervise, direct, and motivate staff; ensures department leaders proactively recognize and solve issues. Drives sales and marketing efforts in collaboration with the community sales leader to meet or exceed occupancy or revenue targets by assisting to develop new business, generate leads, and build strategic relationships.

Aurora, IL30+ days ago

The Infection Preventionist coordinates investigations of patient, staff, or visitor infections and/or suspected exposures and reports to appropriate internal personnel or departments and external agencies. Position Requirements: + Bachelor’s degree in Nursing required with a strong background in clinical microbiology, or related clinical healthcare field, preferably, a minimum of 5 years experience in infection control practices.

Chicago, Illinois30+ days ago

$175,000–$210,000 Per Year

Previous MSL experience in the pharmaceutical/biopharmaceutical industry required with previous respiratory infectious disease experience preferred; experience in COVID-19 preferred OR, previous MSL experience in the pharmaceutical/biopharmaceutical industry preferred with previous respiratory infectious disease experience required. As a clinical and scientific expert on the company and products, the MSL is responsible for building long-term relationships and establishing rapport with HCPs in hospitals, clinics, and academic centers through scientific disease state and product discussions that support current therapeutic concepts and ensure the safe and effective use of products.

New!

Chicago, IL6 days ago

$45–$49 Per Hour

By applying to this job, you agree to receive calls, AI-generated calls, text messages, and/or emails from Atrium and its affiliates, and contracted partners. Guided by our Applicant-Centric™ approach, we foster an environment of collaboration, high performance, and innovation where your talents are valued, and your achievements are celebrated.

Arlington Heights, IL30+ days ago

Directs Quality Control Manager and Quality Assurance/Regulatory Affairs Manager. Periodically reports status of quality control and operations to executive leadership and, when required, regulatory agencies.

Chicago, IL30+ days ago

$125,000–$165,000 Per Year

This role will also play a key part in the execution of commercial offtake arrangements (Power Purchase Agreements (PPAs) , Build-Transfers (BTAs), Development Transfers (DTAs) or Asset Purchases (APAs). The ideal candidate brings utility-scale energy commercial experience, a strong bias for action, broad understanding of energy markets, and experience leading internal and external stakeholder conversations.

Itasca, Illinois30+ days ago

The 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.

Chicago, IL30+ days ago

$176,500–$330,900 Per Year

We are committed to attracting and retaining a diverse workforce and create welcoming, truly inclusive work environments — environments that enable every ADM colleague to feel comfortable on the job, make meaningful contributions to our success, and grow their career. With industry-advancing innovations, a complete portfolio of ingredients and solutions to meet any taste, and a commitment to sustainability, we give customers an edge in solving the nutritional challenges of today and tomorrow.

New!

Chicago, IL5 days ago

You will be involved with working with sales, marketing, customers and vendors to track incoming requests, gathering significant amount of data, data entry and reporting required information to customers in a timely manner. Through comprehensive benefits (https://www.wesco.com/us/en/our-company/careers/work-at-wesco.html#benefits) and active community engagement, we create an environment where every team member has the opportunity to thrive.

Chicago, IL30+ days ago

$94,827–$154,315 Per Year

The HR Compliance Manager is responsible for the leadership, oversight and management of all regulatory and compliance processes within Human Resources, and ensures adherence to Human Resources regulatory requirements, maintaining and updating HR policies and processes, and offering expert consultation on compliance-related matters. + Regularly and proactively conducts HR compliance audits, assesses and identifies areas of potential risk or documentation deficiencies, and implements and leads process improvements and corrective actions where necessary.

Chicago, IL30+ days ago

$128,800–$238,900 Per Year

We are committed to attracting and retaining a diverse workforce and create welcoming, truly inclusive work environments — environments that enable every ADM colleague to feel comfortable on the job, make meaningful contributions to our success, and grow their career. If hired, employees will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

Chicago, Illinois15 days ago

$110,000–$138,000 Per Year

Partner with Clinical Development, Regulatory Affairs, Pharmacovigilance, device development, labeling, non-clinical and other cross‑functional teams to provide GxP guidance and quality support. This position supports the development, execution, and continuous improvement of the company’s clinical quality system, helping to safeguard patient safety, data integrity, and regulatory readiness across all clinical programs.

Chicago, IL30+ days ago

Good communication skills: Strong communication (verbal and written) and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and communicate complex concepts to senior management and regulatory agencies. The successful candidate will play a key role in creating a funding plan to support the Op Plan and all other planning sessions, support preparation of the ALCO meeting and support of strategic initiatives across multiple functions.

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Regulatory Affairs Jobs in Schiller Park, IL

Jobs

Associate Director Regulatory AffairsLundbeck

Director US Regulatory StrategyLundbeck

Engineer, Principal RegulatoryConstellation Energy

Regulatory Labeling SpecialistMedline Industries - Transportation & Operations

Director U.S. Patient AdvocacyLundbeck

Adverse Event SpecialistMedline Industries - Transportation & Operations

Spec Adverse EventsMedline Industries - Transportation & Operations

Principal ToxicologistMedline Industries - Transportation & Operations

Senior Regulatory Affairs ProfessionalVersiti, Inc.

Medical Director IIIUS Tech Solutions, Inc.

Regulatory Affairs Specialist/Senior SpecialistTrinite Consulting Group

Director Regulatory AffairsDairy Management Inc.

Sr Director, Regulatory & Scientific Affairs, Health & WellnessADM

Senior Manager, Regulatory Affairs - Device (Hybrid Onsite)AbbVie

Medical Director, Global Medical Affairs - RemoteAgios Pharmaceuticals

Director, Government AffairsBrunswick

Senior Manager, Government Affairs & Public PolicyCyrusOne

Regional Vice President of Communications & External AffairsPrime Healthcare Management Inc

Quality and Regulatory EngineerFortive Corporation

Engineer, Principal RegulatoryConstellation Energy Generation, LLC.

Clinical Research Regulatory CoordinatorRush University Medical Center

Senior Regulatory Compliance AnalystWarrior Insurance Network

Senior Regulatory Compliance ConsultantWipfli Advisory LLC

Financial Institution Regulatory Compliance Senior ConsultantBaker Tilly Advisory Group, LP

Managing Assistant General Counsel (Government & Regulatory Compliance)ARCO a Family of Construction Companies

Senior Regulatory Compliance AnalystPreferred Risk Insurance

Regulatory Compliance Engineer - RF, Radar and CellularAddison Group

Quality Compliance Lab ManagerSterling Engineering, Inc.

Senior Director, Global Scientific Communications and Publications - RemoteAgios Pharmaceuticals

Associate Director, Product Management – Animal NutritionAjinomoto Health & Nutrition North America, Inc.

Associate Product Counsel, Payments ProductsGoogle

Associate General Counsel - Carelon ServicesElevance Health

Quality SpecialistFortive Corporation

Lead Product StewardshipHoneywell

Medical Review ManagerXeris Pharmaceuticals, Inc.

Director, Engineering - Transmission LineQuanta Infrastructure Solutions Group, LLC

Executive DirectorBrookdale Senior Living

Infection PreventionistRush Copley Medical Center

Medical Science Liaison - COVID/Virology - MidwestShionogi Inc.

Vigilance Report WriterAtrium

Director of QualityCoyote Technical & Executive Sourcing

Manager, Commercial OriginationInvenergy

Quality Assurance ManagerMRINetwork Jobs

Associate General Counsel IT & Cybersecurity - Chicago, ILADM

Analyst - Environmental Product ComplianceWESCO

HR Compliance ManagerRush University Medical Center

Senior Counsel, Mergers & Acquisitions- Chicago, ILADM

Clinical Quality Assurance (CQA) ManagerXeris Pharmaceuticals, Inc.

AVP, Treasury - Financial Planning and AnalysisSynchrony

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