Medline IndustriesRegulatory Labeling Specialist Medline IndustriesRegulatory Labeling SpecialistChicago, IL$79,000–$119,000 / yearFull timeKnowledge 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).
Medline IndustriesPrincipal Toxicologist Medline IndustriesPrincipal ToxicologistNorthfield, IL$152,880–$229,320 / yearFull timeMust 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.
Agios PharmaceuticalsSenior Director, Global Scientific Communications and Publications - Remote Agios PharmaceuticalsSenior Director, Global Scientific Communications and Publications - RemoteChicago, ILRemote$229,562–$344,342 / yearThe 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.
Medline IndustriesSpec Adverse Events Medline IndustriesSpec Adverse EventsMundelein, IL$67,000–$101,000 / yearFull timeEvaluate 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.
Treehouse FoodsNewSenior Manager, Food Safety & Quality Compliance Treehouse FoodsSenior 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).
LundbeckNewSenior Medical Science Liaison Rare Epilepsies- North Central LundbeckSenior Medical Science Liaison Rare Epilepsies- North CentralDeerfield, IL$180,000–$220,000Strategic Scientific Engagement & Insight Generation: Establishes and sustains deep, longitudinal scientific partnerships with Key Opinion Leaders (KOLs), Centers of Excellence, and investigators working in rare epilepsies. This role serves as a strategic pre-launch scientific partner to external experts and internal stakeholders, generating high-quality, actionable insights that inform evidence strategy, disease education, portfolio decision-making, and launch readiness.
Dentsply SironaNewSenior Director, Clinical Education and Events Dentsply SironaSenior Director, Clinical Education and EventsChicago, ILThis leader serves as the senior clinical authority for NAM education, ensuring programs meet the needs of practicing clinicians while supporting business priorities, product adoption, and long term customer trust. • Oversee planning and execution of clinical educational events (e.g., courses, workshops, symposia, webinars), ensuring end-to-end operational excellence (logistics, faculty coordination, attendee experience) and alignment to learning objectives.
Alera GroupDirector of Individual Insurance Compliance & Regulatory Affairs Alera GroupDirector of Individual Insurance Compliance & Regulatory AffairsChicago, IllinoisThe ideal candidate brings deep expertise in Medicare and individual insurance compliance, strong regulatory knowledge, and experience building scalable compliance frameworks within complex, multi-site insurance or healthcare environments. This role will lead the development, implementation, and oversight of scalable compliance programs supporting Medicare Advantage, Medigap, Part D, ACA, and ancillary insurance products across a national distribution platform.
Dairy Management Inc.Director Regulatory Affairs Dairy Management Inc.Director Regulatory AffairsRosemont, IL$99,000–$120,000The 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.
Trinite Consulting GroupRegulatory Affairs Specialist/Senior Specialist Trinite Consulting GroupRegulatory Affairs Specialist/Senior SpecialistRosemont, ILContractorPartner 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.
University of ChicagoRegulatory 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.
Versiti, Inc.Senior Regulatory Affairs Professional Versiti, Inc.Senior Regulatory Affairs ProfessionalAurora, IllinoisThis 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.
ConfidentialNewVice President, Regulatory Affairs ConfidentialVice President, Regulatory AffairsChicago, ILVice President, Regulatory AffairsAbout the CompanyWell-funded biotechnology (BioTech) companyIndustryBiotechnologyTypePrivately HeldAbout the RoleThe Company is in search of a VP of Regulatory Affairs to take on a founding role in building and leading its global regulatory function. This senior leadership position is pivotal, as the successful candidate will be responsible for developing and executing the global regulatory strategy, serving as the primary regulatory voice and strategic advisor across various functions, and leading all major regulatory submissions and interactions with health authorities.
Metropolitan Family ServicesGovernment Affairs & Policy Associate Metropolitan Family ServicesGovernment Affairs & Policy AssociateChicago, IL$60,000–$65,000 / yearPart timeCoordinate and assist with adopted Government Affairs & Policy projects through project lifecycle including draft project proposals, monitor project progress, communicate with project team members and stakeholders, conduct research to support project planning and decision-making, and provide general administrative support to ensure successful delivery of tangible and intangible project outcomes. Metropolitan is Illinois’ first comprehensive human services agency and reaches more than 205,000 individuals and families in Chicago, Evanston/Skokie, the southwest suburbs and DuPage County with services promoting education, economic stability, emotional wellness and empowerment.
Metropolitan Family ServicesManager of Government Affairs & Policy Metropolitan Family ServicesManager of Government Affairs & PolicyChicago, IL$75,000–$80,000 / yearPart timeReporting to the Vice President of Policy and Government Affairs, the Manager supervises Government Affairs & Policy Associates and Policy Analysts (and if applicable, interns) and ensures effective coordination and collaboration across departmental and agency-wide policy development, research, advocacy communications, and legislative engagement efforts. Metropolitan is Illinois’ first comprehensive human services agency and reaches more than 205,000 individuals and families in Chicago, Evanston/Skokie, the southwest suburbs and DuPage County with services promoting education, economic stability, emotional wellness and empowerment.
Ingredion IncDirector 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.
Dairy Management Inc.Senior Director Scientific Affairs Dairy Management Inc.Senior Director Scientific AffairsRosemont, IL$117,000–$135,000NDC 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. Collaborate with cross-functional teams including Nutrition Research, Nutrition Affairs, Sustainability Affairs and Communications team to interpret and translate science to develop educational resources, POVs and scientific symposia (e.g., ASN) .
MRA Recruiting ServicesMedical Affairs Operations Manager MRA Recruiting ServicesMedical Affairs Operations ManagerMcHenry, ILFull timeAs one of the largest employer associations in the nation, MRA helps its member organizations thrive by offering the most comprehensive assortment of HR services, information, education, and resources to help build successful workplaces and a powerful workforce. This role is a critical connector across Medical Affairs, Clinical, Sales, Marketing, and external healthcare partners to ensure successful delivery of scientific and educational programs that improve outcomes in maternity and neonatal care.
Molson Coors Beverage CompanyVP Communications & Corp Affairs Molson Coors Beverage CompanyVP Communications & Corp AffairsChicago, IL$214,800–$281,900 / yearJob Posting Total Rewards Offerings : $214,800.00-$281,900.00 (posting salary range) + 35% target short term incentive + target long term incentive + $23,000 on average spent on benefits per employee, including but not limited to health, dental, vision, retirement with above market employer match, wellness incentives and EAP + paid time off (including holidays, vacation days and sick days). As a senior member of the Legal, Communications & Government Affairs leadership team, you will act as a strategic advisor to the CEO and executive leadership, guiding the organization through complex business, regulatory, and reputational environments.
Prime Healthcare Management IncRegional Vice President of Communications & External Affairs Prime Healthcare Management IncRegional Vice President of Communications & External AffairsEvanston, Illinois$165,000–$190,000 / yearResponsibilities: 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.
CyrusOneSenior Manager, Government Affairs & Public Policy CyrusOneSenior Manager, Government Affairs & Public PolicyAurora, ILThe 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.
Bell Flavors and FragrancesRegulatory Coordinator Bell Flavors and FragrancesRegulatory CoordinatorNorthbrook, IL$50,000–$60,000 / yearPart timeAs a Regulatory Coordinator, you’ll play a critical role in ensuring our products meet local, national, and international regulations while supporting both internal teams and external customers. Bell Flavors & Fragrances is a global leader in developing innovative products for the food, beverage, cosmetic, personal care, and household care industries.
Amgen IncUnited States Regulatory Lead - Obesity and Related Conditions TA Amgen IncUnited States Regulatory Lead - Obesity and Related Conditions TADeerfield, IL$153,935–$184,298 / yearPreferred Qualifications: • Regulatory submissions experience and demonstrated experience interacting with regulatory agencies (FDA) • Strong knowledge of the U.S. regulatory environment and drug development lifecycle • Experience developing/implementing regulatory strategy, including risk management and contingency planning • Experience leading U.S. labeling strategy, negotiation, and timeline management in a cross-functional setting • Strong communication and influencing skills; ability to drive alignment and resolve conflicts • Experience working with policies, procedures, and SOPs in a regulated environment • Experience supporting programs in Obesity, Diabetes, or related metabolic diseases. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of: • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan • Stock-based long-term incentives • Award-winning time-off plans • Flexible work models where possible.
MercorNewRegulatory Compliance Expert - Risk Specialist - AI Trainer MercorRegulatory Compliance Expert - Risk Specialist - AI TrainerChicago, IllinoisRemote$1,150–$1,450Annotate, label, and validate data across compliance use cases like control testing and regulatory change management. Create realistic scenarios based on compliance and risk workflows such as regulatory examinations and internal audit findings.
Fortive CorporationQuality and Regulatory Engineer Fortive CorporationQuality and Regulatory EngineerGlenwood, IL$88,000–$147,000 / yearExecute 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.
Constellation Energy Generation, LLC.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.
Tempus AI IncManager, Regulatory Submissions Tempus AI IncManager, Regulatory SubmissionsChicago, IL$110,000–$150,000 / yearExperience with: • Premarket Approval (PMA) applications, de novo Requests for Reclassification, 510(k)s, Investigational Device Exemption (IDE) requirements • Ex-US, CE Marking, UKCA registration, performance studies as required under IVDR and MDR • Software validation and risk management • Cybersecurity in medical devices • Machine learning validation requirements • Lifecycle management of medical devices/IVDs • Changes to medical devices or IVDs, including those that trigger reporting or regulatory submissions • Relevant sections of 21 CFR 820/ISO 13485, 21 CFR 812, CAP/CLIA • Strong communication, presentation, and interpersonal skills • Experience guiding cross-functional teams of subject matter experts • Experience working in a startup-like environment • Experience interacting with regulators • Ability to work well with quality, clinical, medical, bioinformatics, and laboratory teams across a variety of therapeutic areas • Responsive to feedback, willing to change direction, and able to identify creative solutions to meet business and regulatory needs • Excellent attention to detail • Strong project management skills and the ability to execute on project plans in a fast-paced environment • Scientific background • PhD preferred • Minimum of 5+ years of experience in Regulatory Affairs experience related to medical devices • Knowledge of engineering concepts and biology with ability to evaluate device performance data and develop testing plans. • Establishing processes for efficiently addressing the requirements of multiple regulatory frameworks at scale • Developing and executing premarket and postmarket regulatory project plans and strategies, including assessments of change controls • Working closely with cross-departmental subject matter experts to guide the creation of documentation needed for regulatory applications and internal records • Working closely with business leadership to ensure regulatory strategy aligns with commercial goals • Making regular reports to our executive team, operationalizing leadership direction quickly and efficiently.
ExelonSr Business Program Manager - Reliability Programs (Regulatory) ExelonSr Business Program Manager - Reliability Programs (Regulatory)OAKBROOK TERRACE, ILWe are a Fortune 200 company, 20,000 colleagues strong serving more than 10.7 million customers at six energy companies -- Atlantic City Electric (ACE), Baltimore Gas and Electric (BGE), Commonwealth Edison (ComEd), Delmarva Power & Light (DPL), PECO Energy Company (PECO), and Potomac Electric Power Company (Pepco). This position has a direct impact on the Company's performance regarding several key indicators: operational costs, System Average Interruption Frequency Index (SAIFI), Customer Average Interruption Duration Index (CAIDI) and Customer Satisfaction by managing scope, budget and schedule to within approved parameters, and providing structured and detailed reports to the appropriate Management team.
ComEdSr Business Program Manager - Reliability Programs (Regulatory) ComEdSr Business Program Manager - Reliability Programs (Regulatory)OAKBROOK TERRACE, IllinoisThis position has a direct impact on the Company's performance regarding several key indicators: operational costs, System Average Interruption Frequency Index (SAIFI), Customer Average Interruption Duration Index (CAIDI) and Customer Satisfaction by managing scope, budget and schedule to within approved parameters, and providing structured and detailed reports to the appropriate Management team. We are a Fortune 200 company, 20,000 colleagues strong serving more than 10.7 million customers at six energy companies -- Atlantic City Electric (ACE), Baltimore Gas and Electric (BGE), Commonwealth Edison (ComEd), Delmarva Power & Light (DPL), PECO Energy Company (PECO), and Potomac Electric Power Company (Pepco).
Baker Tilly Advisory Group, LPFinancial Institution Regulatory Compliance Senior Consultant Baker Tilly Advisory Group, LPFinancial Institution Regulatory Compliance Senior ConsultantChicago, IllinoisBaker 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.
Navistar International CorpRegulatory Compliance Engineer Navistar International CorpRegulatory Compliance Engineerlisle, ILCompany Overview ABOUT TRATON With its brands Scania, MAN, International, and Volkswagen Truck & Bus, TRATON SE is the parent and holding company of the TRATON GROUP and one of the world's leading commercial vehicle manufacturers. ABOUT INTERNATIONAL From a one-man company built on the world-changing invention of the McCormick reaper in 1831, to the 15,000-person-strong company we are today, few companies can lay claim to a history like International.
Addison GroupRegulatory Compliance Engineer - RF, Radar and Cellular Addison GroupRegulatory Compliance Engineer - RF, Radar and CellularHoffman Estates, Illinois$100,000–$160,000 / yearThis role ensures that products perform exactly as claimed and meet all regulatory requirements prior to release. Preparing FCC filings, test reports, and certification documentation.
ARCO a Family of Construction CompaniesManaging Assistant General Counsel (Government & Regulatory Compliance) ARCO a Family of Construction CompaniesManaging Assistant General Counsel (Government & Regulatory Compliance)Downers Grove, IllinoisYou 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.
ExelonNewSr Regulatory Specialist ExelonSr Regulatory SpecialistOAKBROOK TERRACE, ILWe are a Fortune 200 company, 20,000 colleagues strong serving more than 10.7 million customers at six energy companies -- Atlantic City Electric (ACE), Baltimore Gas and Electric (BGE), Commonwealth Edison (ComEd), Delmarva Power & Light (DPL), PECO Energy Company (PECO), and Potomac Electric Power Company (Pepco). Under the direction of the Regulatory Compliance Manager, act as a conduit for regulatory compliance matters including but not limited to all records management matters to/from ComEd and Exelon, track and report ongoing commitments, and support other regulatory compliance policies and procedures.
Preferred Risk InsuranceSenior Regulatory Compliance Analyst Preferred Risk InsuranceSenior Regulatory Compliance AnalystBedford Park, IL$70,000–$95,000 / yearThe 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.
ComEdNewSr Regulatory Specialist ComEdSr Regulatory SpecialistOAKBROOK TERRACE, IllinoisWe are a Fortune 200 company, 20,000 colleagues strong serving more than 10.7 million customers at six energy companies -- Atlantic City Electric (ACE), Baltimore Gas and Electric (BGE), Commonwealth Edison (ComEd), Delmarva Power & Light (DPL), PECO Energy Company (PECO), and Potomac Electric Power Company (Pepco). Under the direction of the Regulatory Compliance Manager, act as a conduit for regulatory compliance matters including but not limited to all records management matters to/from ComEd and Exelon, track and report ongoing commitments, and support other regulatory compliance policies and procedures.
Xeris Pharmaceuticals, Inc.Associate Director, Marketing Rare Disease Xeris Pharmaceuticals, Inc.Associate Director, Marketing Rare DiseaseChicago, Illinois$170,000–$195,000 / yearThis individual will collaborate closely with Marketing leads and cross-functional partners, including Medical Affairs, Regulatory, Sales, Market Access, Commercial Operations, Compliance, and Patient Access, to ensure all initiatives align with brand objectives and Xeris’ commitment to improving patients’ lives. Partner with Medical Affairs, Clinical, Regulatory, and Market Access around the design of potential Phase IV studies, RWE initiatives, and additional clinical studies to support label expansion; provide commercial perspective aligned with brand strategy to guide decision making.
Ajinomoto Health & Nutrition North America, Inc.Associate Director, Product Management – Animal Nutrition Ajinomoto Health & Nutrition North America, Inc.Associate Director, Product Management – Animal NutritionItasca, Illinois$180,000–$205,000 / yearOverview: 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.
Ajinomoto Cambrooke, Inc.Associate Director, Product Management – Animal Nutrition Ajinomoto Cambrooke, Inc.Associate Director, Product Management – Animal NutritionItasca, Illinois$180,000–$205,000 / yearOverview: 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.
Shionogi Inc.Medical Science Liaison - COVID/Virology - Midwest Shionogi Inc.Medical Science Liaison - COVID/Virology - MidwestChicago, Illinois$175,000–$210,000 / yearPrevious 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.
Sterling Engineering, Inc.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.
Shirley Ryan AbilityLabNewVice President, Chief Nursing Officer Shirley Ryan AbilityLabVice President, Chief Nursing OfficerChicago, IL$275,000–$400,000 / yearThe VP, Chief Nursing Officer (CNO) sets and advances Shirley Ryan AbilityLab's nursing vision, translates strategy into practice and champions a differentiated culture that empowers nurses to deliver exceptional patient care. The CNO will consistently demonstrate support of the Shirley Ryan AbilityLab statement of Vision, Mission and Core Values by striving for excellence, contributing to the team efforts and showing respect and compassion for patients and their families, fellow employees, and all others with whom there is contact at or in the interest of the institute.
LivaNova PlcDirector - Product Security LivaNova PlcDirector - Product SecurityChicago, ILRemote$185,000–$225,000 / yearKey Responsibilities: Strategic Leadership & Program Management: • Define and execute a comprehensive product security strategy that aligns with business priorities, FDA/MDR/524B expectations, and Quality Management System (QMS) requirements. • Manage the generation and maintenance of SBOMs and VEX (Vulnerability Exploitability eXchange) documents to ensure transparency and enable targeted, actionable risk management for regulators and customers.
Beam TherapeuticsSenior Medical Science Liaison/Medical Science Liaison – Chicago Region Beam TherapeuticsSenior Medical Science Liaison/Medical Science Liaison – Chicago RegionChicago, ILRemote$180,000–$225,000 / yearThis Director (or Associate Director) level MSL will own a defined US territory with primary responsibility in sickle cell disease (SCD) and shared accountability across the Beam pipeline, including Alpha‑1 antitrypsin deficiency (Alpha‑1) and glycogen storage disease 1a (GSD). Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.
TephraNewDirector Business Development MedTech QA & RA Solutions-EIS : Me TephraDirector Business Development MedTech QA & RA Solutions-EIS : MeChicago, ILFurther, they will provide technical leadership, guide engineering and development for complex medical devices equipment/systems, and work with functional areas across the organization (MedTech COE, AI COE, Manufacturing, R&D/NPI, Quality & Regulatory) to deliver best-in-class solutions and capabilities. Where needed, in an owner or supporter role, RFP responses, drafts proposals, plans phased project execution, develops detailed project plans and manages program budgets and costs; fosters shared accountability for the results-based implementation plan.
Rose InternationalNewResearch & Development Clinical Scientist Jobs in USA, IL, Cary | Rose International Job Rose InternationalResearch & Development Clinical Scientist Jobs in USA, IL, Cary | Rose International JobTrout Valley, IL$40–$42 / hourTemporaryRequired Education: Bachelor's degree in chemistry Required Experience/Skills: 6+ years of hands-on experience with analytical instrumentation, including HPLC, GC, FTIR, UV-Vis, and related laboratory equipment. Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify).
LivaNova PlcHead of Sales, OSA LivaNova PlcHead of Sales, OSAChicago, IL$325,000–$430,000 / yearMinimum of 10 years' experience managing large national sales teams, including Director level positions and 2 levels of management across the U.S. • Proven success launching and scaling medical device or therapy-based products. • Experience in working with cross-functional teams on organizational design, sales force deployment, performance management, incentive compensation design, product launch and talent management strategies required.
ADMAssociate General Counsel IT & Cybersecurity - Chicago, IL ADMAssociate General Counsel IT & Cybersecurity - Chicago, ILChicago, IL$176,500–$330,900 / yearWe 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.
Brookdale Senior LivingExecutive Director Brookdale Senior LivingExecutive DirectorVernon Hills, ILFull timeSupervises, 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.
Quanta Infrastructure Solutions Group, LLCDirector, Engineering - Transmission Line Quanta Infrastructure Solutions Group, LLCDirector, Engineering - Transmission LineChicago, IllinoisThe 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.