1,378 Results for

Regulatory Specialist Jobs in Ohio

Jobs

Dayton, OH

Remote

$69,920–$133,620 / year

Proactively manages assigned claims caseload comprised of complex damages that require commensurate knowledge and understanding of claims coverage including potential legal liability. 2 years of relevant property claims adjusting experience of moderate complexity losses that includes writing estimates, involving dwelling and structural damages.

Today

Elyria, OH

$45,000–$52,000

Vaco/Highspring does not have knowledge of the tools used by its clients in making final hiring decisions and cannot opine on their use of AI products.

Vaco by Highspring values a diverse workplace and strongly encourages women, people of color, LGBTQ+ individuals, people with disabilities, members of ethnic minorities, foreign-born residents, and veterans to apply.

Determining compensation for this role (and others) at Vaco by Highspring depends upon a wide array of factors including but not limited to:

the individual’s skill sets, experience and training;
licensure and certification requirements;
office location and other geographic considerations;
other business and organizational needs.

7 days ago

Columbus, OH

$50,000–$60,000

p> Determining compensation for this role (and others) at Vaco by Highspring depends upon a wide array of factors including but not limited to:

the individual’s skill sets, experience and training;
licensure and certification requirements;
office location and other geographic considerations;
other business and organizational needs.
Canadian residents may access our policies in English here and in French here.

7 days ago

Cincinnati, OH

$92,500–$171,500 / year

Please click here for the E-Verify Poster in English or Spanish.

Extensive analog and digital circuit design, microcontrollers, data acquisition, filtering/conditioning, printed circuit design, measurement error analysis, and future system-level engineering.

2 days ago

Uniontown, OH

$18–$23

p style="outline:none;margin-top:0px;margin-bottom:1rem;line-height:1.25;color:rgb( 38 , 35 , 33 );font-family:'circular' , '-apple-system' , 'blinkmacsystemfont' , 'segoe ui' , 'roboto' , 'oxygen' , 'ubuntu' , 'cantarell' , 'fira sans' , 'droid sans' , 'helvetica neue' , sans-serif;font-size:16px;font-style:normal;font-weight:400;letter-spacing:normal;text-indent:0px;text-transform:none;word-spacing:0px;white-space:normal;background-color:rgb( 255 , 255 , 255 )">Securitas Technology Offers Comprehensive Benefits Including .

Opportunity for annual merit pay increases.

17 days ago

Columbus, OH

The Payroll Specialist at Contract Lumber is responsible for ensuring accurate and timely payroll processing for all employees. Day to Day:

Accurately execute payroll process for all employees, including salaried and hourly workers.

Today

New London, OH

We are looking for an EHS and Quality Engineer/Specialist for our New London, OH location with responsibility for ensuring day-to-day compliance with Primetals Quality Management System and Environmental, Health and Safety Program at the local level to maintain ISO and EPA certifications. This position reports to organizational level VP of Quality and EHS for Primetals Technologies USA and functional level to General Manager in New London, OHlocation, ensuring alignment with both strategic goals and operational objectives.

30+ days ago

Findlay, Ohio

p>Duty 4: Identify opportunities related to clinical documentation and/or other system enhancements to support optimal and accurate charge processes; collaborate with CDI Specialist, Claims Resolution Specialist, Revenue Integrity Auditor, Revenue Integrity Educator, clinical area, and other areas to support resolution of issues.

The primary purpose of the Professional Coding Integrity Specialist (PCIS) is to review, enter and/or modify charges as appropriate, including review of clinical documentation to ensure charge is supported and/or to determine specific charge/modifier assignments, for designated clinical areas.

30+ days ago

Chillicothe, OH

$59,059.65–$90,000 / year

Qualifications Competitive candidates must demonstrate: Experience as a Property Field Inspection Claim Specialist in the insurance industry, specifically in property claims Strong knowledge of property insurance policies, coverage and claim handling practices Knowledge of both residential and commercial building construction Familiarity with local regulations and compliance requirements in your assigned territory Excellent communication and interpersonal skills to effectively interact with clients, agents, and other stakeholders Proven effective communication skills to handle difficult/emotional conversations with a customer-minded focus Proven ability to assess damages, estimate repair costs, and negotiate settlements Detail-oriented with strong organizational and analytical skills Proficient in using claims management software and other relevant tools Physical agility to allow for: frequent lifting, carrying and climbing a ladder; ability to navigate roofs at various heights for inspection of both residential and commercial structures; ability to crawl in tight spaces May be required to complete Rope and Harness Safety Training. A valid driver's license is required Preferred: Bachelor's Degree in a related field or equivalent work experience Experience in handling complex or high-value claims Construction background Water mitigation inspection experience Xactimate, XactContents Additional Details: Employees must successfully complete all required training, including applicable proficiency, licensing exam(s), Motor Vehicle Record (MVR) checks, and background checks required of various state(s).

3 days ago

Findlay, Ohio

li class="MsoNoSpacing">Duty 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.

30+ days ago

Findlay, Ohio

30+ days ago

Findlay, Ohio

30+ days ago

New Albany, OH

$116,255–$151,132.50 / year

The 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.

30+ days ago

New Albany, Ohio

The 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.

1 day ago

Cleveland, Ohio

Our diverse product portfolio includes category leading brands such as Reese’s Pinworm®, Reese’s Colotest® and new brands such as LiceGuard® As Reese focuses on an aggressive growth strategy, we are looking for a technical and insight driven Assistant Controller to help take our business to the next level. Founded in 1907 and headquartered in Cleveland, Ohio, Reese Consumer Health is a consumer-first, insight-driven company with nearly 120 years of expertise in manufacturing, marketing, and collaborating with retailers.

Today

Westlake, OH

Instead, the position focuses on supporting commercial teams, supply chain operations, and customers by maintaining high-quality product compliance across a diverse, multi-supplier portfolio.

This position sits at the intersection of product data integrity, regulatory compliance, and product stewardship, ensuring that product information, regulatory classifications, and compliance processes are accurate, scalable, and aligned with evolving domestic and international regulations.

30+ days ago

Cuyahoga Falls, Ohio

This 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.

30+ days ago

Brecksville, OH

Position Summary: This position is responsible for preparing submissions to various regulatory agencies - most notably those pertaining to FDA 510(k) premarket notifications. Assist with the preparation and submission of regulatory filings, including FDA 510(k) premarket notifications and product listings.

26 days ago

Bowling Green, OH

The successful candidate will work independently and collaborate with cross-functional teams to lead small projects, evaluate product changes, maintain regulatory approvals, and manage regulatory databases. COMMUNICATIONS-ORAL AND WRITTEN: Is able to write and speak clearly and succinctly in a variety of communication settings and styles; can get messages across that have the desired effect.

5 days ago

Cincinnati, OH

$75,000–$100,000 / year

As a Regulatory Specialist you will be responsible for providing regulatory support to internal and external customers to ensure Ditsch is compliant to all legal and customer requirements. The quality of our irresistible products comes from more than 100 years of experience and craftsmanship in the ART OF PRETZEL MAKING!

19 days ago

Cincinnati, OH

$18–$20.67 / hour

This includes all Bank Secrecy Act, Anti-Money Laundering, OFAC and Suspicious Activity reporting requirements, as well as all other lending and deposit compliance requirements.

Must demonstrate the ability to change priorities quickly, handle multiple priorities, work effectively under time constraints, and contribute to the team effort.

9 days ago

Medina, OH

Sandridge needs your passion and skill to deliver on our promise to always provide great tasting fresh food with consistent hand-made quality that enhances the reputation of our customers Join our team of food innovators and technicians to produce fresh, delicious food that will make it to tables across the country.

The ideal candidate will collaborate cross-functionally with Operations, R&D, Quality, Sales, and Customer Service to support product commercialization, regulatory compliance, and continuous improvement initiatives.

21 days ago

Avon Lake, OH

p>Additionally, 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.

29 days ago

New Albany, OH

Individual 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.

30+ days ago

Cincinnati, OH

li>Directing the development of permit applications, including Special Use Permits for actions on federal lands, Section 404/401 permits, Virginia Water Protection permits, Virginia Stormwater Management Permits, Virginia Marine Resources permit, Tennessee Valley Authority (TVA) permits, involving gathering supporting documentation, and coordinating comment response with agencies.

Directing the development of technical reports for the US Army Corps of Engineers (USACE), US Fish and Wildlife Service (USFWS), Virginia Department of Environmental Quality (VDEQ), Virginia Marine Resources Commission (VMRC), Federal Highway Administration (FHWA), Environmental Protection Agency (EPA), Virginia Department of Historic Resources (VDHR) and other federal, state, and local agencies.

12 days ago

Cleveland, Ohio

General: 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.

Today

Cincinnati, OH

The 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.

30+ days ago

Mentor, OH

$58,100–$62,000 / year

ul>

Responsible for investigating and managing complaints for potential reporting under the FDA Medical Device Reporting regulations and applicable international regulations, preparing draft complaint summaries and MDR/Vigilance reports for presentation to the Reportable Events Committee for review, and maintaining documentation in accordance with department policies, procedures, and work instructions.

Strong interpersonal skills - ability to work closely with people at all levels within the STERIS organization and facilitate the implementation of corrective actions; able to work effectively and professionally with external people including Customers and government officials.

30+ days ago

Blue Ash, OH

Ensure 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.

30+ days ago

Cincinnati, OH

$150,000–$205,000 / year

The Director works as part of the Regulatory Affairs team to monitor regulatory activity, coordinate calls and meetings, develop advocacy documents such as comments and letters, help the team prepare for panels and hearings, develop presentations, and provide other assistance as needed. The Director Regulatory Affairs works to advance the Regulatory Affairs Departments mission of promoting the wireless industrys positions on Federal regulatory policy issues on behalf of and in coordination with CTIAs members.

30+ days ago

Columbus, OH

Responsible 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.

30+ days ago

Cincinnati, OH

p>The Global Senior Manager, Regulatory Affairs serves as the senior regulatory leader for Gentherm Medical, responsible for developing and executing regulatory strategies that support global market access, product lifecycle management, and business growth. This role partners closely with executive leadership to assess regulatory risks and opportunities, provides strategic guidance on regulatory matters, and leads interactions with global regulatory authorities.

8 days ago

Columbus, OH

Remote

You 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.

Today

Troy, OH

$109,000–$159,000 / year

Reporting to the Director of Food Safety, Quality & Regulatory Affairs, you will lead food safety, quality, and regulatory programs at our Troy, Ohio manufacturing facility, producing products such as Slim Jim, meat snacks, and frozen bakery items. Knowledge of food safety principles, manufacturing processes, and regulatory requirements including Global Food Safety Initiative, Food Safety Modernization Act, FDA, and USDA.

1 day ago

Mason, OH

MAJOR DUTIES AND RESPONSIBILITIES FDA 510(k) submission o Conduct comprehensive review of technical documentation (design controls, V&V, risk, labeling, clinical evidence, and software as applicable) to ensure completeness, quality, and regulatory compliance o Perform detailed regulatory gap assessments against FDA requirements (21 CFR Parts 807, 820, and applicable FDA guidance documents) o Author, compile and deliver a complete 510k submission, including preparation in FDA eSTAR format, o Lead submission lifecycle activities, including: o Acceptance Review support (RTA readiness) o Substantive Review coordination o Drafting and submission of responses to FDA requests for Additional Information, Interactive review communications o Updating submission content and modules as required o Interface cross-functionally to incorporate Business inputs and ensure alignment throughout the review process. This role is a hand-on, execution-focused contractor position responsible for reviewing technical documentation, ensuring regulatory compliance, authoring submission materials, and supporting documentation regulatory strategies across US, EU and global markets.

4 days ago

Cincinnati, OH
Lead regulatory intelligence efforts globally - monitoring emerging regulatory trends (e.g., EU MDR, China NMPA, LATAM registrations) and proactively advising executive leadership on strategic implications. The Director will represent Gentherm Medical with regulatory authorities worldwide and ensure regulatory alignment is embedded into commercialization, portfolio planning, and long-term product lifecycle decisions.
30+ days ago

Cincinnati, OH
We are seeking a Regulatory Affairs Principal to play a key role in advancing our pipeline, including the BreathID platform-a unique combination product at the intersection of pharmaceuticals and diagnostics. The Regulatory Affairs Principal will provide strategic regulatory leadership to support the development, approval, and lifecycle management of pharmaceutical and combination drug-device products.
30+ days ago

Marysville, Ohio
Be 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).
19 days ago

New
Troy, OH
$109,000–$159,000 / year
div>
Reporting to the Director of Food Safety, Quality&Regulatory Affairs, you will lead food safety, quality, and regulatory programs at our Troy, Ohio manufacturing facility, producing products such as Slim Jim, meat snacks, and frozen bakery items.
Knowledge of food safety principles, manufacturing processes, and regulatory requirements including Global Food Safety Initiative, Food Safety Modernization Act, FDA, and USDA.
1 day ago

New
Mason, OH
p>This role is a hand-on, execution-focused contractor position responsible for reviewing technical documentation, ensuring regulatory compliance, authoring submission materials, and supporting documentation regulatory strategies across US, EU and global markets.
We are seeking an experienced Regulatory Affairs contractor to support the preparation and submission of a US FDA 510k and the development of global regulatory documentation, including EU MDR Class IIa readiness and technical documentation.
5 days ago

New
Columbus, OH
$99,300–$198,700 / year
Depending 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.
6 days ago

Columbus, Ohio
Depending 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.
7 days ago

Reynoldsburg, OH
Your 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.
13 days ago

Wakeman, OH
Part time
This includes projects and daily tasks associated with maintaining compliance with domestic quality system as required for Medical Device Manufacturers involved with Clean Room Operations, and through support of other functional departments or product staff in assisting the QA/RA Manager. Prepares quality documentation (ERTs, CRTs and Management Review) and reports by collecting, analyzing, and summarizing information and trends including failed processes, stability studies, recalls, corrective actions, and re-validations.
30+ days ago

OH
We 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.
30+ days ago

Marysville, Ohio
Be 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. 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.
30+ days ago

New
Dublin, OH
Remote
$105,100–$150,100 / year
Symbol 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.
1 day ago

Marysville, OH
$77,200–$90,800 / year
li>
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.
Agency Correspondence Management: Document and track all incoming formal correspondence from regulatory bodies, including the EPA and State Departments of Agriculture, maintaining a centralized repository for registration actions.
30+ days ago

Cincinnati, OH
Provide technical leadership and project management for oil & gas midstream permitting projects (FERC-regulated natural gas or liquids pipeline projects) and energy transition projects throughout the US. Primary Location: United States | IL | Chicago Organization: 1937 EnvSvcs-US Great Lakes East-Chicago IL Employee Status: Regular Business Justification: New Position Travel: No Schedule: Full time Job Posting: 21/04/2026 02:04:51 Req ID: 1005490.
30+ days ago

Mason, Ohio
Regulatory responsibilities also include post-approval drug product reporting activities such as completing regulatory impact assessments for commercial drug product changes, filing labeling and promotional material submissions, supporting adverse event reporting activities and developing appropriate regulatory strategies to support business objectives. Prepare and file FDA labeling and promotional material submissions and communicate dissemination dates to appropriate personnel.10Provide support and/or oversight for outsourced pharmacovigilance activities and file safety report submissions with the FDA or other authorities as necessary.
30+ days ago

Stand out to leading employers.

Upload your resume and let employers find you for new Regulatory Specialist job openings. Plus, receive relevant job matches delivered straight to your inbox.

Create A Free Account

Regulatory Specialist Jobs in Ohio

Property Adjuster Specialist - Field USAA

Accounts Payable Specialist Vaco LLC

AP Specialist Vaco LLC

Specialist, Electrical Engineering (FOS) L3Harris Technologies

Collections Specialist Securitas Technology

Payroll Specialist needed in the Great State of Ohio Contract Lumber

EH&S Engineer/Specialist Primetals Technologies

HIS - Professional Coding Integrity Specialist - 40 hrs/wk, 1st shift Blanchard Valley Health System

Claim Specialist - Property Field Inspection State Farm Mutual Automobile Insurance Company

PFS Facility Medical Billing Specialist - 40 hrs/wk, 1st shift Blanchard Valley Health System

PFS Facility Medical Billing Specialist (PRN) Blanchard Valley Health System

PFS Professional Medical Billing Specialist (PRN) Blanchard Valley Health System

Transmission Regulatory Affairs Specialist Staff American Electric Power Co Inc

Transmission Regulatory Affairs Specialist Staff American Electric Power

Regulatory Affairs Specialist Reese Consumer Health

Consumer & Life Sciences Regulatory Specialist Palmer Holland Inc

Lead Regulatory Affairs Specialist Coltene

Regulatory Affairs Specialist Applied Medical Technology Inc

Regulatory Affairs Specialist Betco Corp

Regulatory Specialist Ditsch

Regulatory Specialist I First Financial Bank NA

Regulatory Compliance Specialist Sandridge Food Corp

Senior Specialist, Regulatory Avient Corp

Regulatory Specialist II Bath & Body Works Inc

Senior Regulatory Specialist Stantec Inc

Audit and Regulatory Specialist Medical Service Company

Regulatory Complaint Specialist - 545 Wollborg Michelson Recruiting

Quality & Regulatory Compliance Specialist Steris Plc

Regulatory Complaint Specialists Tranzeal Inc.

Director, Regulatory Affairs CTIA

Senior Manager, Regulatory Affairs ADMA Biologics Inc

Senior Manager, Regulatory Affairs Gentherm Inc

Senior Regulatory Affairs Consultant (Program / Client Partnership Manager) Parexel

Food Safety, Quality & Regulatory Affairs Manager (Onsite) Conagra Brands Inc

Regulatory Affairs Contractor The Kemtah Group, Inc.

Global Director of Regulatory Affairs Gentherm Inc

Regulatory Affairs Principal, Pharmaceutical and Combination Products Meridian Bioscience Inc

Manager, Regulatory Affairs ScottsMiracle-Gro

Food Safety, Quality&Regulatory Affairs Manager (Onsite) ConAgra Foods

Regulatory Affairs Contractor Belcan LLC

Regulatory Affairs Project Manager - Nutrition - Columbus OH/Abbott Park, IL (internal OUS) Abbott Laboratories

Regulatory Affairs Project Manager - Nutrition - Columbus OH/Abbott Park, IL (internal OUS) Abbott

Manager, Regulatory Affairs Victoria's Secret & Co

Quality Engineering and Regulatory Affairs Intern Exsurco Medical, Inc.

Regulatory Affairs Manager (Transplant Diagnostics) Thermo Fisher Scientific Inc

Analyst, Regulatory Affairs ScottsMiracle-Gro

Regulatory Affairs Manager - Labeling Cardinal Health Inc

Analyst, Regulatory Affairs and Compliance The Scotts Miracle-Gro Co

Senior Environmental Regulatory Permitting Manager - FERC Stantec Inc

Manager of Regulatory Affairs Aprecia Pharmaceuticals

Similar Job Searches