NewRegulatory Affairs Associate III # 26-21316 US Tech Solutions, Inc.Regulatory Affairs Associate III # 26-21316North Chicago, ILThis role oversees the Regulatory Affairs Issue and CAPA Management system (RAIM), triages issue records, escalates issues to Exception Reports when warranted, and partners cross-functionally to drive process improvements. Through collaboration with functional and cross-functional stakeholders, the position also supports inspection readiness and audit/inspection response activities, and management of change plans for legacy company integrations into Regulatory Affairs business processes.
NewRegulatory Affairs Associate I (RIMs) - # 26-21255 US Tech Solutions, Inc.Regulatory Affairs Associate I (RIMs) - # 26-21255North Chicago, ILMonitors activity in COSMOS (Regulatory Information Management solution) for assigned products and activities, including ensuring completeness and accuracy of data. US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions.
NewAdverse Event Specialist MedlineAdverse Event SpecialistMundelein, IL$67,000–$101,000 / yearEvaluate 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.
NewQuality and Compliance Specialist TrovaQuality and Compliance SpecialistElgin, IL$70,000–$90,000 / yearOverview If you’re energized by solving quality problems before they reach customers—and you’re at home navigating supplier performance, documentation, and regulatory requirements—this role puts you at the center of product integrity across the supply chain. Bring your quality mindset, compliance rigor, and supplier-facing confidence—apply today and help build the systems that keep products compliant, customers confident, and performance moving forward.
NewCorporate Quality Lab Technician Pretium Packaging L.L.C.Corporate Quality Lab TechnicianAurora, ILWe are seeking a detail-oriented and technically skilled Corporate Quality Lab Technician to support laboratory testing, quality assurance initiatives, regulatory compliance activities, and continuous improvement efforts across our manufacturing network. Position Overview The Corporate Quality Lab Technician performs analytical testing, physical performance evaluations, equipment verification, and quality data collection for packaging products, components, raw materials, and quality improvement projects.
NewQuality Lab Technician Pretium Packaging - USAQuality Lab TechnicianSaint Charles, ILWe are seeking a detail-oriented and technically skilled Corporate Quality Lab Technician to support laboratory testing, quality assurance initiatives, regulatory compliance activities, and continuous improvement efforts across our manufacturing network. Position Overview The Corporate Quality Lab Technician performs analytical testing, physical performance evaluations, equipment verification, and quality data collection for packaging products, components, raw materials, and quality improvement projects.
NewCORPORATE COUNSEL I NOW HEALTH GROUP, INC.CORPORATE COUNSEL IBloomingdale, ILProvide legal services and assist the Company’s various functional teams’ (operations, engineering, domestic and international sales, quality and science, marketing, private label, finance and accounting, credit and collections, customer service, supply and purchasing, technical, IT and retail) strategies and implementation, to include, but not be limited to, label review, contract drafting and review, legal research, leasing issues and agreements, and prosecution, protection and enforcement of domestic and international intellectual property rights. Assist with the administration of the Company’s general liability, products liability, and workers compensation insurance policies; interface with insurance agents of the Company as needed; ensure the Company has received and provided certificates of liability insurance from vendors; with involvement of customer service, sales and marketing, and quality teams, handle product complaint records (PCRs) from domestic and international customers.
NewRegulatory Affairs Associate I Actalent IncRegulatory Affairs Associate INorth Chicago, IL$66–$72 / hourProject manage Exception Reports in partnership with cross-functional stakeholders to identify root causes, define corrective and preventive actions, and drive continuous improvement in business processes. Collaborate with Regulatory Affairs leaders, Business Process Owners, Quality, and other functional partners to ensure issue management activities are well-coordinated, effective, and aligned with organizational objectives.
NewRegulatory Affairs Associate Katalyst HealthCares & Life Sciences IncRegulatory Affairs AssociateNorth Chicago, ILThis role oversees the Regulatory Affairs Issue and CAPA Management system (RAIM), triages issue records, escalates issues to Exception Reports when warranted, and partners cross-functionally to drive process improvements. Through collaboration with functional and cross-functional stakeholders, the position also supports inspection readiness and audit/inspection response activities, and management of change plans for legacy company integrations into Regulatory Affairs business processes.
Regulatory Affairs Associate Katalyst Healthcares & Life SciencesRegulatory Affairs AssociateNorth Chicago, ILThis role oversees the Regulatory Affairs Issue and CAPA Management system (RAIM), triages issue records, escalates issues to Exception Reports when warranted, and partners cross-functionally to drive process improvements. Through collaboration with functional and cross-functional stakeholders, the position also supports inspection readiness and audit/inspection response activities, and management of change plans for legacy company integrations into Regulatory Affairs business processes.
Regulatory Affairs Associate Karwell TechnologiesRegulatory Affairs AssociateNorth Chicago, ILWhether you're a recent graduate or early in your Regulatory Affairs career, this role provides valuable exposure to regulatory operations, global submissions, data governance, and cross-functional collaboration within a highly respected life sciences environment. Partner with global and regional teams to ensure regulatory submissions and correspondence are accurately documented and aligned across markets.
NewRegulatory Affairs Associate I K3 InnovationsRegulatory Affairs Associate INorth Chicago, ILMonitors activity in COSMOS (Regulatory Information Management solution) for assigned products and activities, including ensuring completeness and accuracy of data. Required Education: Bachelor's degree in related life sciences (pharmacy, biology, chemistry, medical technology pharmacology).
Director, Head of Regulatory Affairs Allstate Insurance CompanyDirector, Head of Regulatory AffairsIL$187,000–$260,000 / yearReporting to the SVP, Government & Industry Relations, the Head of Regulatory Affairs establishes enterprise regulatory governance, oversees examinations, filings, and regulatory matters, leads market conduct and remediation strategies, and develops predictive intelligence capabilities to identify emerging risks, anticipate regulatory trends, and mitigate potential business impacts before they escalate into enforcement actions or material issues. Develop and maintains a comprehensive regulatory risk dashboard that tracks complaint ratios by state, line of business, and product against industry benchmarks (NAIC complaint database), along with examination findings, MCAS trends, legislative activity heat maps, and aging of open regulatory inquiries.
Associate Director International Regulatory Affairs Advertising & Promotion-Hybrid AbbVie IncAssociate Director International Regulatory Affairs Advertising & Promotion-HybridILThe Associate Director will be 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. 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.
NewAssociate II, Regulatory Affairs ICU Medical IncAssociate II, Regulatory AffairsLake Forest, IL$67,500–$96,750 / yearWith the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically-essential IV therapy and high-value critical care products for hospital, alternate site, and home care settings. Excellent knowledge of publishing tools, global submission validation tools, Document Management systems, Toolbox, electronic submission gateways, MS Word, Adobe Acrobat including creating PDF hyperlinks and other support software.
Staff Regulatory Affairs Specialist (Pharmaceutical Products) StrykerStaff Regulatory Affairs Specialist (Pharmaceutical Products)Cary, IllinoisHowever, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. Experience preparing, authoring, or supporting drug regulatory submissions, including submissions for product approvals, post-approval changes, or lifecycle management activities.
Senior Associate, Regulatory Affairs (Hybrid - Lake Forest, IL) ICU Medical Inc.Senior Associate, Regulatory Affairs (Hybrid - Lake Forest, IL)Lake Forest, IL$97,500–$139,750 / yearWith the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically-essential IV therapy and high-value critical care products for hospital, alternate site, and home care settings. Our focus allows us to bring you: Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an effective barrier against bacterial transfer and colonization.
Senior Associate, Regulatory Affairs ICU Medical IncSenior Associate, Regulatory AffairsLake Forest, IL$97,500–$139,750 / yearWith the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically-essential IV therapy and high-value critical care products for hospital, alternate site, and home care settings. Our focus allows us to bring you: Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an effective barrier against bacterial transfer and colonization.
NewSenior Manager, Regulatory Affairs AMETEK IncSenior Manager, Regulatory AffairsMount Prospect, ILEnsure compliance with applicable regulatory requirements, including FDA QMSR, EU Medical Device Regulation (MDR), Medical Device Reporting (MDR), UDI/GUDID, product and site registrations, cybersecurity requirements, Software as a Medical Device (SaMD), CE Marking, labeling requirements, adverse event reporting, field corrective actions, Declaration of Conformity, Buy American Act (BAA), Build America Buy America Act (BABAA), and Certificates of Free Sale. The successful candidate serves as a strategic advisor and subject matter expert on regulatory matters, drives continuous improvement initiatives, supports regulatory inspections and audits, and proactively identifies emerging regulatory trends and requirements that may impact Rauland products, processes, and business objectives.
Senior Associate Regulatory Affairs Submission Management - Hybrid AbbVie IncSenior Associate Regulatory Affairs Submission Management - HybridNorth Chicago, ILWith input from the submission teams, this individual establishes and maintains submission content planners and associated timelines, facilitates tactical submission team meetings, prepares content planners for publishing, interfaces with publishing vendor, and fulfills Submission Management functions on Project Teams in support of Development, Marketing, and post-marketing regulatory authority applications. Responsibilities: Manages medium to high impact (with respect to internal visibility, risk, complexity and criticality) submission projects to ensure the timely delivery of high-quality dossiers that meet technical specifications defined by regulatory authorities and can be easily navigated and reviewed by a regulatory agency.