NewDirector MISO Regulatory Affairs American Municipal Power, IncDirector MISO Regulatory AffairsColumbus, OHFull timeMust possess excellent communication, presentation, diplomacy, active listening, and facilitation skills to effectively work in small or large group forums ranging from technical to non-technical audiences at all levels of the corporate hierarchy. Preferred to have knowledge of capacity, energy, ancillary services market rules, market settlements, applicable FERC orders, applicable MISO and NAESB rules, and emerging generation and transmission technologies.
NewRegulatory Reporting Specialist CYNET SYSTEMSRegulatory Reporting SpecialistMASON, OH$38–$43 / hourTemporaryContractorPart timeAs a nationally and locally certified Minority Business Enterprise (MBE), Cynet Systems is committed to helping organizations build high-performing teams while empowering professionals to grow rewarding careers. We deliver agile, scalable talent solutions across IT, engineering, life sciences, clinical, and professional staffing, powered by a high-performing recruitment engine operating across North America and Asia.
NewEHS Specialist JobotEHS SpecialistZanesville, OH$70,000–$85,000 / yearAir & Waste Compliance (Core Focus): Manage complex environmental regulatory and permit requirements, with a heavy emphasis on Title V Air Permits and RCRA hazardous waste management (preferably for a Large Quantity Generator). Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.
Quality Assurance Specialist (QAS) I SOFIEQuality Assurance Specialist (QAS) IOakwood Village, OH$33–$36 / hourEnsure that components, containers, closures, in-process materials, packaging materials, labeling, and finished dosage forms are examined and approved or rejected to ensure that all these meet their current specifications. Maintain oversight of the QA program and Quality Management System (QMS) at a single SOFIE manufacturing facility producing products under both 21 CFR Part 212 and 211 (as needed) regulations.
NewLoan Funding Specialist Erie HomeLoan Funding SpecialistToledo, OHYou’ll combine traditional loan processing duties—reviewing documents, clearing stipulations, and ensuring lender compliance—with credit analysis to identify potential paths for lender approval. Erie Home has been recognized as a top workplace by The Plain Dealer, is a multi-year recipient of Top Workplaces USA by Energage, and is Great Place to Work® Certified™ .
NewAdministration Specialist (Auto) AtriumAdministration Specialist (Auto)Columbus, OHThis role ensures accurate, compliant, and timely handling of titles and related documentation across multiple states, working closely with borrowers, dealerships, DMVs, and internal teams to support a seamless post-funding experience. Preferred Experience/Skills for the Administration Specialist (Auto): 1 - 3 years of experience in auto title administration, auto finance, dealership title work, or a related field.
Research Specialist - Credit BC ForwardResearch Specialist - CreditColumbus, OH$23–$24 / hourFull timeThe ideal candidate will have strong experience in credit documentation, client due diligence, data stewardship, and portfolio administration and a proven ability to execute in a fast-paced operations environment with accurate data input and clear communication . With delivery centers and offices across North America and India, we take pride in building long-term relationships and delivering excellence through innovation, collaboration, and integrity.
Denials Management Specialist - 40 hrs/wk, 1st shift Blanchard Valley Health SystemDenials Management Specialist - 40 hrs/wk, 1st shiftFindlay, OhioThe specialist will work with multiple departments, including but not limited to, patient access, provider clinics, clinical departments, managed care, billing, coding, and compliance to resolve any outstanding issues which is preventing payments for covered services. The denials management specialist will assist in identifying denials trends, research payer policies, understand coding guidelines, and provide assistance in finding resolution to prevent identified denial trends.
NewVendor Relations & Data Specialist, Purchasing Services, Administration & Finance University of CincinnatiVendor Relations & Data Specialist, Purchasing Services, Administration & FinanceCincinnati, OHAssume ownership of at least two defined purchasing or supplier maintenance work processes, including: responsibility for maintaining current job aids, step-by-step instructions, and reference materials; updating documentation to reflect policy, process, or system changes; and serving as a point of contact for questions related to assigned processes. Home to more than 53,600 students, 12,000 faculty and staff, and over 360,000 living alumni, UC, a Carnegie 1 institution, combines research prowess with a physical setting The New York Times has called “the most ambitious campus design program in the country."
NewProgram Manager-PEG/DAG Public Affairs, Journeyman- WAX 1.4.06 CredenceProgram Manager-PEG/DAG Public Affairs, Journeyman- WAX 1.4.06Wright-Patterson Air Force Base, OHAssist in developing program management strategies to include recommending, initiating, reviewing, developing and implementing activities to accomplish Business Case Analysis (BCA), Cost of Ownership analysis (COO), aging aircraft analysis, process documentation, PWSs, Statement of Work (SOWs), Data Item Descriptions (DIDs), test plans, acquisition plans, Life Cycle Management Plans (LCMPs), Life Cycle Sustainment Plans (LCSPs) Engine Life Management Plans (ELMPs), Quality Assurance Surveillance Plans (QASPs), Acquisition Strategy Panels (ASPs), IMPs, IMSs, Aircraft Information Programs (AIPs), and Aircraft Information Management Plans (AIMPs). Support key acquisition events and reviews as needed, such as: System Requirements Reviews (SRRs), Preliminary Design Reviews (PDRs), Critical Design Reviews (CDRs), Test Readiness Reviews (TRRs), Technical Coordination Meetings (TCMs), Functional Configuration Audits (FCAs), Physical Configuration Audits (PCAs), Production Readiness Reviews (PRRs), Technical Interchange Meetings (TIMs), and others as applicable.
PFS Facility Medical Billing Specialist - 40 hrs/wk, 1st shift Blanchard Valley Health SystemPFS Facility Medical Billing Specialist - 40 hrs/wk, 1st shiftFindlay, OhioDuty 3: Corrects all claims issues prior to submission which may be, but are not limited to, quality audits of patient demographic information and insurance eligibility, cross referencing with previous services, verifying payer authorizations, identifies and bills missing and late charges and corrects all necessary discrepancies. Duty 9: Identifies high-risk accounts, prioritizes follow up efforts, efficiently contacts various insurance payors to determine reasons for outstanding claims and proactively communicates to facilitate timely payment of submitted claims.
PFS Professional Medical Billing Specialist (PRN) Blanchard Valley Health SystemPFS Professional Medical Billing Specialist (PRN)Findlay, OhioDuty 3: Corrects all claims issues prior to submission which may be, but are not limited to, quality audits of patient demographic information and insurance eligibility, cross referencing with previous services, verifying payer authorizations, identifies and bills missing and late charges and corrects all necessary discrepancies. Duty 9: Identifies high-risk accounts, prioritizes follow up efforts, efficiently contacts various insurance payors to determine reasons for outstanding claims and proactively communicates to facilitate timely payment of submitted claims.
PFS Facility Medical Billing Specialist (PRN) Blanchard Valley Health SystemPFS Facility Medical Billing Specialist (PRN)Findlay, OhioDuty 3: Corrects all claims issues prior to submission which may be, but are not limited to, quality audits of patient demographic information and insurance eligibility, cross referencing with previous services, verifying payer authorizations, identifies and bills missing and late charges and corrects all necessary discrepancies. Duty 9: Identifies high-risk accounts, prioritizes follow up efforts, efficiently contacts various insurance payors to determine reasons for outstanding claims and proactively communicates to facilitate timely payment of submitted claims.
Senior Regulatory Specialist HDR IncSenior Regulatory SpecialistCleveland, OH$106,820–$152,600 / yearStates-Ohio-Cleveland'',''United States-Ohio-Cleveland'','''','''','''','''','''','''','''','''',''Water'',''Water'',''Full-time'',''Full-time'',''Regular'',''Regular'','''','''',''Utility Management Services'',''Utility Management Services'',''Aug 7, 2026'',''Aug 7, 2026'',''false'',''789356'',''789356'',''true'',''789356'',''false'',''Submission for the position: Senior Regulatory Specialist - (Job Number: 195126)'',''false'',''789356'',''false'',''true''. Technical duties developing and implementing compliance strategies to mitigate regulatory impacts; include independently reviewing NPDES permits, Total Maximum Daily Load Studies, and new or pending regulations from the context of representing regulated clients; reviewing and analyzing water quality and hydrologic data; applying water quality models; and directing others.
Lead Regulatory Affairs Specialist ColteneLead Regulatory Affairs SpecialistCuyahoga Falls, OhioThis includes providing regulatory guidance, registering products, evaluating engineering changes with respect to regulatory compliance, maintaining required regulatory records and reports and interacting with regulatory agencies and notified bodies. Interface with cross-functional teams on large and small projects to ensure products are transferred to production in accordance with cGMPs, QSRs, MDRs and the Quality Management System.
NewRegulatory Affairs Specialist GlobalchannelmanagementRegulatory Affairs SpecialistWestlake, OhioRegulatory Affairs Specialist duties: Responsible for classifying new and existing products according to the Globally Harmonized System of Classification and Labeling of Chemicals (GHS). Pre-Authoring of Safety Data Sheets (SDS) and labels in accordance to Haz Comm 2012 and WHMIS 2015.
Regulatory Specialist SMX, LLCRegulatory SpecialistWestlake, OHRemote$23–$26 / hourCollaborate with cross-functional teams including Product Development, Quality, Marketing, and Supply Chain to support new product introductions and resolve regulatory questions. With Staff Management | SMX, you'll get a weekly paycheck, learn new skills, meet new people, and work with a great management team in a clean and safe environment.
Regulatory Affairs Specialist, EHS, North America Henry Schein IncRegulatory Affairs Specialist, EHS, North AmericaOH$56,604–$88,443 / yearDevelop and deliver employee environmental, health, and safety (EHS) awareness and training programs to ensure compliance with applicable federal, state, and international regulations, including OSHA, OSHA State Plans (e.g., Cal/OSHA), DOT, IATA, IMO, and EPA requirements. Proficient in Microsoft Office applications, including PowerPoint, and experienced with project management methodologies and tools commonly used in the medical device or pharmaceutical industries.
Regulatory Specialist - Corporate Services Center Trinity HealthRegulatory Specialist - Corporate Services CenterColumbus, OHBroad based clinical or management leadership experience with knowledge of complex systems and systems change with demonstrated success in tactical and analytical thinking. Serves as liaison between offsite hospital services and Mount Carmel services to support the hospitals' regulatory requirements.
Chemical Regulatory Specialist GlobalchannelmanagementChemical Regulatory SpecialistOhioExperience with chemical inventories, SDS management, hazardous waste handling, and EHS documentation systems. Chemical Regulatory Specialist requires: OSHA, EPA, RCRA, DOT, and related regulatory frameworks.
Clinical Research Regulatory Specialist I, College of Medicine, Internal Medicine, Remote University of CincinnatiClinical Research Regulatory Specialist I, College of Medicine, Internal Medicine, RemoteCincinnati, OHRemoteServe as liaison for questions/issues for designated research protocols and performs submissions to Institutional Review Boards (IRBs) including initial submissions, continuing reviews, amendments, reportable events, and/or closure. Home to more than 53,600 students, 12,000 faculty and staff, and over 360,000 living alumni, UC, a Carnegie 1 institution, combines research prowess with a physical setting The New York Times has called "the most ambitious campus design program in the country."
Operations Regulatory Specialist II (Hybrid location) CareSourceOperations Regulatory Specialist II (Hybrid location)Dayton, OH$62,700–$100,400 / yearJob Summary: The Operations Regulatory Specialist II provides analytical support and leadership for key internal Operations projects and partners with the Operations departments to ensure all regulatory and compliance deliverables are met. CareSource takes into consideration a combination of a candidate's education, training, and experience as well as the position's scope and complexity, the discretion and latitude required for the role, and other external and internal data when establishing a salary level.
Regulatory Specialist - Corporate Services Center Trinity Health CorporationRegulatory Specialist - Corporate Services CenterColumbus, OHBroad based clinical or management leadership experience with knowledge of complex systems and systems change with demonstrated success in tactical and analytical thinking. Serves as liaison between offsite hospital services and Mount Carmel services to support the hospitals' regulatory requirements.
REGULATORY SPECIALIST COORD Premier Health PartnersREGULATORY SPECIALIST COORDDayton, OHThe incumbent is the organizational expert with focused responsibilities in leading Regulatory Compliance including the Joint Commission (TJC), Centers for Medicare and Medicaid (CMS), Ohio Department of Health (ODH), and other local, state and federal agencies, including the TJC disease specific certifications. Respiratory or other clinically focused disciplines who support the clinical needs of patient populations.
Senior Specialist, Regulatory Avient CorpSenior Specialist, RegulatoryAvon Lake, OHAdditionally, the applicant must have employment experience with: (1) Applying all applicable regulations related to Hazard Communication (North America, Europe, Asia, etc.), such as GHS, EU CLP and other regional regulations; (2) Working with North American regulatory agencies such as EPA, FDA, or FIFRA to assist in product registrations, and submissions; (3) Maintaining all relevant product information within the SAP EH&S Module and other PS systems provide data for various reports; (4) Obtaining and maintaining compliance information on various raw materials to support customer requests related to REACH, RoHS, TSCA, Prop 65; and. By playing to win, acting customer centric, driving innovation and profitable growth, collaborating seamlessly across Avient, and motivating and inspiring and developing others and yourself you will accelerate your ability to achieve Avient's strategic goals, to meet our customer needs, and to accomplish your career goals.
Food Safety Quality and Regulatory Specialist (Pet Premix) Cargill IncFood Safety Quality and Regulatory Specialist (Pet Premix)Lewisburg, OHThe Food Safety Quality and Regulatory Specialist (Pet Premix) will provide specialized knowledge of specific segments of quality systems or plant processes such as food safety and quality auditing, instrumentation, specific product line knowledge, computer systems, management or oversight of suppliers and other needed focus areas. This position is in our specialized portfolio enterprise where we serve diverse businesses who support unique customers or markets, including animal nutrition and health, bioindustrial, road safety salt and Cargill joint ventures.
Audit and Regulatory Specialist Medical Service CompanyAudit and Regulatory SpecialistCleveland, OhioGeneral: Under the direction of the Director, Regulatory, Compliance and Risk, Ensures compliance with regulations and controls by examining and analyzing records, reports, operating practices, and documentation; and recommending opportunities to strengthen the internal control structure. Responsible for replying to and tracking of external audit activity for a variety of payers including Medicare, Medicaid and commercial payers.
Regulatory Specialist I Bath & Body Works IncRegulatory Specialist INew Albany, OHIndividual contributor responsible for providing day-to-day global regulatory support, execution and advisement for the successful launch and lifecycle of formulated and hardline/softline consumer products such as home fragrance, personal care, OTC drugs and accessories. Key duties include - concept review, ingredient/formula evaluation, label approval, claims, product registrations/notifications, and post-market support with a focus on supporting global franchise partners around the world with product compliance!
Regulatory Complaint Specialist - 545 Wollborg Michelson RecruitingRegulatory Complaint Specialist - 545Cincinnati, OHThe specialist reviews escalated cases filed with state and federal regulators, conducts thorough investigations, and delivers clear, well-supported decisions that align with regulatory requirements and internal policies. Lead end-to-end investigations of escalated regulatory complaints and dispute cases, including gathering evidence, reviewing account activity, and analyzing relevant documentation.
Senior Specialist, Regulatory Avient CorporationSenior Specialist, RegulatoryAvon Lake, OHFull timeBy playing to win, acting customer centric, driving innovation and profitable growth, collaborating seamlessly across Avient, and motivating and inspiring and developing others and yourself you will accelerate your ability to achieve Avient's strategic goals, to meet our customer needs, and to accomplish your career goals. We believe that all of our global employees are leaders and that the six most important behaviors for driving our strategy and culture are the same no matter if an employee is a leader of self, a leader of others, or a leader of the business.
Regulatory Specialist II Givaudan SARegulatory Specialist IICincinnati, OH$65,000–$70,000 / yearYou work within an inspiring teamwork culture - where you can thrive, collaborate and learn from other talented and passionate people across disciplines, regions and divisions. Provide internal customers with consistent and compliant formula reviews and documentation to meet global commercial, creation and research initiatives.
Sr. Environmental Regulatory Specialist Ross Environmental Services, IncSr. Environmental Regulatory SpecialistElyria, OHPart timeDevelops, maintains and implements cross-functional programs and project plans to accomplish departmental and corporate goals and objectives for all EHS regulatory programs (e.g., RCRA and CAA permitting; customer auditing; waste vendor auditing, Transportation program evaluation and regulatory analysis). Acts as a departmental liaison and trainer, technical expert, and regulatory consultant to RIS Operations, RIS Technology, RES Sales, RES Marketing, RES Technical Services, RTS, and new business ventures.
NewRegulatory Reporting Specialist Tailored ManagementRegulatory Reporting SpecialistMASON, OH$43.57 / hourThe Analyst serves as the primary owner of recurring report production activities and maintains reporting schedules, validation guides, and operational documentation while supporting issue investigation, audit requests, and reporting quality initiatives. This role supports day-to-day Regulatory Reporting operations by ensuring report deliveries are accurate, timely, and compliant with established requirements.
Regulatory Complaint Specialists Tranzeal Inc.Regulatory Complaint SpecialistsBlue Ash, OHEnsure regulatory timeframes as well as internal Service Level Agreements [SLA] are met to avoid compliance violations, which include, but are not limited to issuance of credit, reversal of fees, interest reimbursement, mailing appropriate notification letters to customers, case closure timeframes, decision accuracy, account closures/blocks, etc. At we continually seek individuals with a keen passion for delivering exceptional customer experiences, a desire to make an impact, a commitment to their work, the ability to elevate the performance of their team members and display enjoyment for solving complex customer issues.
NewRegulatory Reporting Specialist BelcanRegulatory Reporting SpecialistMason, OHThe Analyst serves as the primary owner of recurring report production activities and maintains reporting schedules, validation guides, and operational documentation while supporting issue investigation, audit requests, and reporting quality initiatives. This role supports day-to-day Regulatory Reporting operations by ensuring report deliveries are accurate, timely, and compliant with established requirements.
NewRegulatory Reporting Specialist Belcan LLCRegulatory Reporting SpecialistMason, OHThe Analyst serves as the primary owner of recurring report production activities and maintains reporting schedules, validation guides, and operational documentation while supporting issue investigation, audit requests, and reporting quality initiatives. This role supports day-to-day Regulatory Reporting operations by ensuring report deliveries are accurate, timely, and compliant with established requirements.
NewRegulatory Reporting Specialist The Kemtah Group, Inc.Regulatory Reporting SpecialistMason, OHThe Analyst serves as the primary owner of recurring report production activities and maintains reporting schedules, validation guides, and operational documentation while supporting issue investigation, audit requests, and reporting quality initiatives. This role supports day-to-day Regulatory Reporting operations by ensuring report deliveries are accurate, timely, and compliant with established requirements.
NewSenior Regulatory Affairs Consultant - Regulatory Project Manager ParexelSenior Regulatory Affairs Consultant - Regulatory Project ManagerColumbus, OHRemoteYou will be accountable for driving regulatory excellence by aligning cross-functional stakeholders, managing complex timelines, and anticipating challenges to enable successful delivery of regulatory milestones that support sponsor's mission to bring transformative vaccines to patients worldwide. This role is designed for an experienced and forward-thinking regulatory project manager who thrives in a fast-paced, innovative environment and can seamlessly integrate strategic thinking with operational execution across all stages of product development, registration, and post-marketing.
NewSenior Director of Regulatory Affairs Cleveland DiagnosticsSenior Director of Regulatory AffairsCleveland, OhioReports to: Chief Medical Officer Job Overview The Senior Director of Regulatory Affairs will provide strategic and operational leadership for regulatory affairs activities supporting Cleveland Diagnostics’ in vitro diagnostic (IVD) and laboratory developed test (LDT) product portfolio, including tests/assays intended for early cancer detection and other clinical indications. The Senior Director will serve as a regulatory leader for FDA-regulated IVD products, including PMA, PMA supplement, 510(k), amendment, annual report, and post-approval submission activities, as well as international regulatory documentation, including IVDR Technical Documentation and other jurisdictional requirements where applicable.
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.
Strategist, Regulatory Affairs ClinChoiceStrategist, Regulatory AffairsCincinnati, OHPrepare and/or review letters of authorization, cover letters for registration certificates, declarations, power of attorney, and other regulatory documentation to ensure accuracy, appropriateness, and consistency of documents intended for various global regulatory submissions. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel.
Strategist, Regulatory Affairs ClinChoice IncStrategist, Regulatory AffairsCincinnati, OHPrepare and/or review letters of authorization, cover letters for registration certificates, declarations, power of attorney, and other regulatory documentation to ensure accuracy, appropriateness, and consistency of documents intended for various global regulatory submissions. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel.
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.
Analyst, Regulatory Affairs and Compliance The Scotts Miracle-Gro CoAnalyst, Regulatory Affairs and ComplianceMarysville, OH$111,500–$131,200 / yearBe 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 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).
NewDirector, Legislative & Regulatory Affairs - Solar Interstate Gas SupplyDirector, Legislative & Regulatory Affairs - SolarOhioThis leadership role drives IGS's legislative and regulatory strategy for its renewable energy businesses, with a primary focus on residential and commercial solar, distributed energy resources (DERs), battery storage, community solar, and emerging clean energy technologies. The Director develops and executes advocacy strategies, builds relationships with regulators and policymakers, influences legislation and regulatory policy, and helps position IGS as a trusted leader in the evolving renewable energy marketplace.
Packaging Compliance Manager/Packaging Engineer in Regulatory Affairs - Columbus OH/Abbott Park, IL (internal OUS can apply) Abbott LaboratoriesPackaging Compliance Manager/Packaging Engineer in Regulatory Affairs - Columbus OH/Abbott Park, IL (internal OUS can apply)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, 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.