Principal Regulatory Affairs Specialist
$80.9k - $127.05kCardinal Health
US-Nationwide-FIELD
IL-Waukegan-MWDC
MA-Mansfield-West Building
Full time
20184380
What Regulatory Affairs contributes to Cardinal Health
Regulatory provides regulatory affairs and product development consulting services to enable pharmaceutical, medical and biotechnology companies to obtain regulatory approvals. This function applies subject matter expertise to provide services in technical writing and regulatory submissions as well as clinical research and manufacturing process consulting. Regulatory Affairs plans, coordinates and implements regulatory strategies for products that require government approval. This job family proactively identifies regulatory requirements and risks for products and develops plans for product development programs and regulatory submissions.
Job Summary
The Principal Regulatory Affairs Specialist will support the Medical Solutions Regulatory affairs team. They are responsible for regulatory activities associated with new product development and maintenance of business projects. This includes being a regulatory lead for change development projects, new product development, change assessment, US, EU and international regulatory submissions, commercial support, manufacturing support, compliance related activities, systems improvement, and other responsibilities aligned with global medical device regulations and the goals of the Medical Solutions business.
Location: This is a remote position, and the ideal candidate will be located near or willing to travel to Waukegan, IL or Mansfield, MA.
Responsibilities
Lead new and modified product development projects to establish and integrate regulatory strategy into project activities.
Lead the preparation, submission, and maintenance of global product registrations with a focus on 510(k), EU Technical Documents, and International STEDs.
Collaborate with internal Cardinal Health international regulatory departments to assess international registration requirements, develop international regulatory strategy, and ensure timely execution.
Review design control documents including documents associated with design inputs and design outputs.
Review product labeling for compliance with global labeling regulations.
Interpret and evaluate proposed regulations for medical devices and advise on impact of such regulations to the business.
Maintain regulatory intelligence through continuous monitoring of regulatory landscape; identify risks, mitigation, and resolution strategies.
Maintain and provide regulatory information in support of customer queries, bid and tender submissions, customs queries, etc.
Development and implementation of regulatory procedures and SOPs.
Qualifications
Bachelor's Degree in a scientific discipline or equivalent work experience, preferred.
5+ years regulatory affairs experience preferred.
Experience in medical device industry a plus.
Proficiency in US and Europe medical devices regulations highly preferred.
Strong organizational and problem-solving skills.
Strong oral and written communication skills.
Ability to manage multiple projects while maintaining deadlines.
Ability to travel up to 10% of the time.
What is expected of you and others at this level
Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects
May contribute to the development of policies and procedures
Works on complex projects of large scope
Develops technical solutions to a wide range of difficult problems
Solutions are innovative and consistent with organization objectives
Completes work; independently receives general guidance on new projects
Work reviewed for purpose of meeting objectives
May act as a mentor to less experienced colleagues
Anticipated salary range: $80,900 - $127,050
Bonus eligible: No
Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being.
Medical, dental and vision coverage
Paid time off plan
Health savings account (HSA)
401k savings plan
Access to wages before pay day with myFlexPay
Flexible spending accounts (FSAs)
Short- and long-term disability coverage
Work-Life resources
Paid parental leave
Healthy lifestyle programs
Application window anticipated to close: 09/25/2026 *if interested in opportunity, please submit application as soon as possible.
The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity.
#LI-Remote
#LI-JD3
Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.
Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.
To read and review this privacy notice click here (
Headquartered in Dublin, Ohio, Cardinal Health, Inc. (NYSE: CAH) is a distributor of pharmaceuticals, a global manufacturer and distributor of medical and laboratory products, and a provider of performance and data solutions for healthcare facilities.
We are a crucial link between the clinical and operational sides of healthcare, delivering end-to-end solutions and data-driving insights that advance healthcare and improve lives every day. With deep partnerships, diverse perspectives and innovative digital solutions, we build connections across the continuum of care.
With more than 50 years of experience, we seize the opportunity to address healthcare's most complicated challenges - now, and in the future.
View Cardinal Health on YouTube (
If your personal information has changed and needs edited, please contact your recruiter for assistance. If you have not yet been contacted by a recruiter, please email us at View email address on click.appcast.io for assistance.
- ...Responsibilities: The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical devices (including Class I and II devices, software...Suggested
- AbbVie’s MPDD function seeks a Principal Scientist II in computational chemistry to shape the vision of computational sciences and to guide stage-appropriate models that accelerate drug candidates. You will lead, pilot, and implement advanced quantum mechanics, molecular...Principal
- AbbVie Process Chemistry seeks a Principal Research Scientist II to drive drug substance process development for small molecules. The... ...across chemistry and engineering. A strong background in GMP and regulatory documentation is essential. The candidate will contribute to...Principal
- AbbVie in North Chicago, IL is seeking a Principal Data Engineer embedded in PDST to design, build, and operate enterprise-grade data... ...data assets used by data scientists and process engineers to accelerate development and regulatory submissions. #J-18808-Ljbffr AllerganPrincipal
- Planet Pharma is seeking a Regulatory Information Management support professional in Illinois. The role focuses on regional regulatory submissions, system-based data stewardship, and ensuring alignment with central data standards. Fresh graduates with relevant life sciences...Suggested
$160.5k - $305k
...toxicology issues as well as select and advance Development compounds. Ability to function in multidisciplinary teams to address regulatory queries. Serves and/or leads issue resolution teams and participates in due diligence teams. Responsible for compliance with...Principal- ...a leadership role in specific CDM tasks (e.g Subject Matter Expert (SME)) Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents Effectively plan and execute multiple Data Management projects...PrincipalWork at office
- ...America's leading distributor of shipping, industrial and packaging materials! As a Senior International Trade Compliance Specialist, you’ll tackle regulatory hurdles, find tariff savings and bring Uline’s high quality products to international destinations.Careers Packed...Full time
- ...toxicology issues as well as select and advance Development compounds. Ability to function in multidisciplinary teams to address regulatory queries. Serves and/or leads issue resolution teams and participates in due diligence teams. Responsible for compliance with...PrincipalLocal area
- ...Qualifications This position can be hired at the Sr. Scientist II or Principal Scientist I level depending on years of experience and... ...and batch record authoring. Hand-on experience with authoring regulatory filings for biologics and sterile parenteral products Experienceleading...PrincipalTemporary work
- ...Description As a discipline expert and technology leader, the Principal AI Engineer II will define and advance the strategy,... ...human oversight, and responsible AI. Partner with Quality, Regulatory, Legal, Privacy, Information Security, scientific, technical,...PrincipalFull timeLocal area
- ...than 170 countries. AbbVie Process Chemistry is seeking a Senior Principal Research Scientist to conduct process research and development... ...strategic and experimental issues. Author and review key regulatory documents, laboratory data, technical memos and reports....PrincipalFull timeWork experience placementLocal areaWorldwide
- ...Qualifications This position can be hired at the Sr. Scientist II or Principal Scientist I level depending on years of experience and... ...batch record authoring. Hand-on experience with authoring regulatory filings for biologics and sterile parenteral products...PrincipalTemporary workLocal area
- ...scientific proposals. Anticipate and critically evaluate scientific, regulatory and competitive advances related to new technological advances... ...biomedical research. Demonstrated ability to function as a principal investigator, generating original technical ideas and research...PrincipalFull timeLocal area
$29 - $32.29 per hour
job summary: Are you a detail-oriented regulatory professional with strong technical project management skills? Join a global pharmaceutical leader in North Chicago, IL, on a hybrid schedule. In this high-visibility execution role, you will act as a Technical Project...Hourly payContract workTemporary workWork experience placement- ...for pipeline molecules and supports the justification of CMC regulatory content. Job Description Role Overview The... ...product development scientists, program managers, and regulatory affairs specialists. Author and/or review technical documents summarizing process...PrincipalTemporary workWork experience placementLocal area
$129.3k - $258.7k
...to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.The OpportunityThe Principal Product Manager for Enterprise Developer Experience defines the vision, strategy, and roadmap for the platforms, tools, and...PrincipalWorldwideShift work- ...Job Description Job Description Job Description As an Assistant Principal at The Menta Education Group, you will support school-wide initiatives that focus on teacher development, implementation of PBIS, and Common Core Standards. Menta Academy North: Waukegan...PrincipalFull timeWork at officeLocal area
- ...Reference26-00999Remote50% Remote Responsibilities: Support regional Regulatory Information Management (RIM) activities using systems such as... ...initiatives. Requirements: Bachelor's degree in Regulatory Affairs, Pharmacy, Health Sciences, or a related discipline Experience...Remote work
- Job-ID32908843Reference26-01550 Summary: The Manager, Process Excellence within Regulatory Affairs is responsible for managing key process excellence and issue management activities that support compliant, efficient, and inspection-ready Regulatory Affairs operations....
- ...coordinate activities with all functional departments in support of regulatory filings.* Manage, compile, and author CMC sections of marketed... ...pharmaceutical experience including 1-2 years in regulatory affairs, R&D, or Manufacturing (CTD Module 3)Responsible for managing...Shift work
- ...environments, activities. Generate new scientific proposals and lead those efforts. Anticipate and critically evaluate scientific or regulatory advances or competitive threats and respond with appropriate new strategies. Recognized and sought out as an expert in his/her...PrincipalFull timeLocal area
- Job Description Job Description Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable...PrincipalLocal area
- ...and integrate this knowledge into new business technology solutions. Responsibilities: Effectively function as the SAP S4 Principal Engineer, generating new technological proposals and leading those efforts. Anticipate and critically evaluate technological advances...PrincipalFull timeWork at officeLocal area
$120k - $150k
...DescriptionJoin the Astronics team as a Principal Staff Electrical Engineer! Job Summary:... ...direction to Ukraine engineers and CAD specialists.Develop and review the creation and... ...into the manufacturing process.Support regulatory compliance testing.Become Subject Matter...PrincipalPart timeLocal areaFlexible hours- Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across...PrincipalFull timeLocal area
- ...Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description AbbVie Information Research seeks a Principal Research Data Scientist to design, architect, and develop AI data solutions that drive the advancement of our AI and machine...PrincipalFull timeWork experience placementLocal area
- ...Science & Technology (PDS&T) is seeking a Principal Research Scientist I to conduct late-... ...Author and review key technical and regulatory documents. The position involves multi... ...example: Manufacturing Operations, Regulatory Affairs, Quality Assurance, etc....PrincipalFull time
- Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across...PrincipalFull timeLocal area
- ...Pharmacy/ Engineering/ Other Related Subject 2. 2-4 years CMC Regulatory experience - Bachelors Degree: Chemistry/ Biology/ Pharmacy/... .... Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research & Development...Remote work
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Principal Regulatory Affairs Specialist. Be the first to apply!



