Transmission Regulatory Affairs Specialist Staff American Electric Power Co IncTransmission Regulatory Affairs Specialist StaffNew Albany, OH$116,255–$151,132.50 / yearThe Transmission Regulatory Affairs Specialist Staff coordinates filing strategy, schedules, testimony development, discovery responses, and compliance with federal and state filing requirements while partnering closely with operating company leadership, legal counsel, finance, operations, and other internal stakeholders. Success requires excellent judgment, communication, and the ability to translate complex regulatory, financial, and operational information into clear, persuasive filings and stakeholder-ready messaging-aligned with AEP's Core Principle of Regulatory Integrity.
NewTransmission Regulatory Affairs Specialist Staff American Electric PowerTransmission Regulatory Affairs Specialist StaffNew Albany, OhioThe Transmission Regulatory Affairs Specialist Staff coordinates filing strategy, schedules, testimony development, discovery responses, and compliance with federal and state filing requirements while partnering closely with operating company leadership, legal counsel, finance, operations, and other internal stakeholders. Success requires excellent judgment, communication, and the ability to translate complex regulatory, financial, and operational information into clear, persuasive filings and stakeholder-ready messaging—aligned with AEP’s Core Principle of Regulatory Integrity.
Regulatory Specialist II Bath & Body Works IncRegulatory Specialist IINew Albany, OHIndividual contributor responsible for providing day‑to‑day global regulatory support, execution, and advisement for the successful launch and lifecycle management of compliant formulated consumer products, including personal care, home fragrance, home care, and OTC drugs. Our management team is dedicated to ensuring fulfillment of this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, associate activities and general treatment during employment.
Senior Manager, Regulatory Affairs ADMA Biologics IncSenior Manager, Regulatory AffairsColumbus, OHResponsible for the preparation, review, presentation, and publishing of all FDA submissions to assure accuracy and completeness of submission documents, which includes but is not limited to meeting requests/briefing packages and presentations to the FDA (e.g., preIND/pre-BLA, end-of-phase II, Type A,B or C, and advisory committee meetings), Investigational New Drug Applications (INDs), Biologic License Applications (BLAs), Orphan Drug Applications, Marketing and Promotional Materials, Product Listing and Establishment License Applications, and other related documents or CMC supplement submissions. Essential Functions and Responsibilities: Provides accurate and timely regulatory guidance to Management, Process Development, Analytical Development, Manufacturing, and the Quality Assurance/Quality Control staff while maintaining frequent contact with the Head of Regulatory Affairs.
NewSenior Regulatory Affairs Consultant (Program / Client Partnership Manager) ParexelSenior Regulatory Affairs Consultant (Program / Client Partnership Manager)Columbus, OHRemoteYou will play a key leadership role in managing midsize to large Regulatory Affairs outsourcing programs, partnering closely with clients and cross-functional teams to drive operational excellence, ensure delivery against regulatory objectives, and support the successful progression of development and commercial programs. Due to continued growth and the ongoing success of our Regulatory Affairs Consulting team, Parexel is seeking an experienced Senior Regulatory Affairs Consultant (Program / Client Partnership Manager) to join our team.
Manager, Regulatory Affairs ScottsMiracle-GroManager, Regulatory AffairsMarysville, OhioBe part of something bigger by joining one of our Employee Resource Groups focusing on diversity and inclusion, family, education and sustainability: Scotts Women’s Network, Scotts Black Employees’ Network, Scotts Veterans Network, Scotts Young Professionals, Scotts Pride Network (GroPride), Scotts Associates for a Greener Earth (SAGE), Scotts Family TREE and our Associate Boards. As a regulatory leader, you will directly manage a team of 5–10 regulatory professionals, driving process improvements, overseeing complex registration projects, and serving as the primary liaison with regulatory agencies (EPA and state departments of agriculture).
Manager, Regulatory Affairs Victoria's Secret & CoManager, Regulatory AffairsReynoldsburg, OHYour Role: The Manager, Global Regulatory Affairs is responsible for leading regulatory strategy and execution across the product lifecycle to ensure compliant, efficient, and successful commercialization of beauty products in global markets. The Manager partners closely with Product Development, R&D, Packaging, Safety, Quality, Legal, and Commercialization teams to embed regulatory and packaging requirements early in development, improve decision-making, and reduce downstream risk.
Regulatory Affairs Manager (Transplant Diagnostics) Thermo Fisher Scientific IncRegulatory Affairs Manager (Transplant Diagnostics)OHWe provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Working closely with cross-functional teams, you'll help develop and implement regulatory strategies that enable the successful commercialization of our advanced products, from initial planning through post-market activities.
Regulatory Affairs Project Manager - Nutrition - Columbus OH/Abbott Park, IL (internal OUS) Abbott LaboratoriesRegulatory Affairs Project Manager - Nutrition - Columbus OH/Abbott Park, IL (internal OUS)Columbus, OH$99,300–$198,700 / yearDepending on specific role, the Regulatory Affairs Project Manager may be involved in various regulatory activities (market access activities, regulatory submissions/registrations; evaluation of product and/or packaging and manufacturing changes for regulatory implications; maintaining compliance documentation, review and approval of label changes, advertising and promotional items; oversight of systems related to product and/or packaging management, project management, process improvement, etc.). Supervisory/Management Responsibilities (Influence/Impact/Leadership): Provide leadership without direct authority (i.e., project leader) and provide direction and guidance to exempt and non-exempt personnel who exercise significant latitude and independence in their assignments.
Regulatory Affairs Project Manager - Nutrition - Columbus OH/Abbott Park, IL (internal OUS) AbbottRegulatory Affairs Project Manager - Nutrition - Columbus OH/Abbott Park, IL (internal OUS)Columbus, OhioDepending on specific role, the Regulatory Affairs Project Manager may be involved in various regulatory activities (market access activities, regulatory submissions/registrations; evaluation of product and/or packaging and manufacturing changes for regulatory implications; maintaining compliance documentation, review and approval of label changes, advertising and promotional items; oversight of systems related to product and/or packaging management, project management, process improvement, etc.). 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.
Analyst, Regulatory Affairs The Scotts Miracle-Gro CoAnalyst, Regulatory AffairsMarysville, OHp>• Be part of something bigger by joining one of our Employee Resource Groups focusing on diversity and inclusion, family, education and sustainability: Scotts Womens Network, Scotts Black Employees Network, Scotts Veterans Network, Scotts Young Professionals, Scotts Pride Network (GroPride), Scotts Associates for a Greener Earth (SAGE), Scotts Family TREE and our Associate Boards. In the absence of a signed Master Service Agreement, and specific approval to submit resumes to an approved requisition, the Scotts Miracle-Gro company will not consider or approve payment regarding recruiter fees or referral compensations.
NewRegulatory Affairs Manager - Labeling Cardinal Health IncRegulatory Affairs Manager - LabelingDublin, OHRemote$105,100–$150,100 / yearSymbol and Mark Management: Ensure the correct application of environmental symbols and marks, including those for the WEEE Directive, battery directives (e.g., crossed-out wheeled bin), recycling (e.g., "Green Dot," Mobius loop), and packaging material identification. Risk Management: Ability to apply risk management principles (ISO 14971) to the labeling process, identifying and mitigating risks associated with labeling errors, such as product recalls, shipping holds, or regulatory enforcement actions.
Analyst, Regulatory Affairs and Compliance The Scotts Miracle-Gro CoAnalyst, Regulatory Affairs and ComplianceMarysville, OH$77,200–$90,800 / yearBe part of something bigger by joining one of our Employee Resource Groups focusing on diversity and inclusion, family, education and sustainability: Scotts Womens Network, Scotts Black Employees Network, Scotts Veterans Network, Scotts Young Professionals, Scotts Pride Network (GroPride), Scotts Associates for a Greener Earth (SAGE), Scotts Family TREE and our Associate Boards. In the absence of a signed Master Service Agreement, and specific approval to submit resumes to an approved requisition, the Scotts Miracle-Gro company will not consider or approve payment regarding recruiter fees or referral compensations.
Quality Manager: Regulatory & Quality Systems Focused American Nitrile, LLCQuality Manager: Regulatory & Quality Systems FocusedGrove City, OHp>The purpose of the Quality Manager - Quality Systems & Regulatory Manager is to develop, implement, maintain, and continuously improve the Quality Management System (QMS) and Regulatory Compliance programs at American Nitrile. The Quality Systems & Regulatory Manager is responsible for the management, compliance, and continuous improvement of both Quality Systems and Regulatory Affairs functions.
LIMS System & Data Specialist II Forge Biologics IncLIMS System & Data Specialist IIColumbus, OHThis role is responsible for building and maintaining test definitions, sample plans, specification requirements and study designs in LIMS to support in-process, release, and stability testing for AAV, plasmid, cell bank, buffer, and raw materials, along with generation of electronic Certificate of Analysis (COA) and Certificate of Testing (COT) documents needed to support batch release or disposition. Acting as a Tier 1 LIMS support resource, this role partners closely with QC subject matter experts, QA, IT, and the LIMS System Administrator to support compliant system use, continuous improvement, and adoption of new LIMS functionality.
Managed Services Sr. Consultant Deloitte Touche Tohmatsu LtdManaged Services Sr. ConsultantOH$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.
Supply Chain Analyst I ResilienceSupply Chain Analyst IOhioThe Supply Chain Analyst I supports supply chain master data activities and system-driven processes that enable new product introductions, ongoing manufacturing operations, and regulatory compliance. This role assists in maintaining accurate data within enterprise systems such as SAP and supports documentation and process activities, bill of materials (BOM), and operational changes.
Compliance Analyst: Licensing & Complaints Gwc Warranty CorporationCompliance Analyst: Licensing & ComplaintsWesterville, OHIn this role, you will play a critical part in maintaining APCO''s regulatory compliance by managing licensing and registration activities, supporting regulatory filings, coordinating consumer complaint responses, and driving process improvements that strengthen our compliance framework. Our teams work collaboratively across operations, technology, risk, finance, marketing, and sales to deliver solutions that create measurable value and support the continued growth of APCO and the partners we serve.