Principal Regulatory Affairs Specialist
$80.9k - $127.05kCardinal Health
Principal Regulatory Affairs SpecialistRegulatory 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 SummaryThe 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.ResponsibilitiesLead 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.QualificationsBachelor'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.Anticipated salary range: $80,900 - $127,050Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being.Medical, dental and vision coveragePaid time off planHealth savings account (HSA)401k savings planAccess to wages before pay day with myFlexPayFlexible spending accounts (FSAs)Short- and long-term disability coverageWork-Life resourcesPaid parental leaveHealthy lifestyle programsApplication window anticipated to close: 08/07/2026 *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.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. Cardinal Health
- ...Astronics SubsidiaryAstronics CSC LocationLake Zurich, IL DescriptionJoin the Astronics team as a Principal Staff Electrical Engineer! Job Summary:Experienced developer with proven ability to design for passing EMI/EMC tests and to troubleshoot and diagnosis EMC/EMI qualification...PrincipalLocal area
- 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- ...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...PrincipalWork at office
- ...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
- ...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
- ...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
- ...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...PrincipalLocal area
- ...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
- ...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
$141.5k
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 several...PrincipalLocal area- 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
- 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
- ...all key partners in the functional departments in support of regulatory filings. Responsibilities: Manage, compile, and author CMC... ...pharmaceutical experience including 1-2 years in regulatory affairs or 1-2 years in Discovery, R&D, or Manufacturing Strong working...Full timeTemporary workWork at officeLocal areaRemote work
- ...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
- ...Description: Working with technical team to prepare regulatory filing dossiers Potentially assessing changes for regulatory... .... Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research & Development...Full time
- ...at . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description The Senior Associate, Regulatory Affairs Submission Management , manages medium to high impact, moderately complex submission projects involving multiple cross-...Full timeTemporary workWork at officeLocal areaRemote work
- 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
- ...’s clinical candidates. We are looking for a highly motivated Principal Research Scientist II who can make scientific contributions and... ...strategic and experimental issues. Author and review key regulatory documents, laboratory data, technical memos and reports. The...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
- ...Job Description The Quantitative, Translational and ADME Science (QTAS) organization at AbbVie is seeking a highly motivated Principal Research Scientist II – Central Core Function Operations Leader to join the Non-regulated Bioanalysis team in North Chicago. This...PrincipalFull timeLocal area
- 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
- ...Instagram , X and YouTube. Job Description Purpose : AbbVie is expanding its presence in Obesity Therapeutics and is seeking a Principal Scientist to participate in external innovation and diligence efforts to advance the early obesity pipeline. This individual will...PrincipalFull timeContract workLocal area
- ...analytical lead on development teams, and contribute to regulatory strategy and scientific innovation and... ...Development, and Quality Assurance and CMC-Regulatory Affairs. Responsibilities: Effectively function as a principal research scientist, generating original...PrincipalFull timeLocal area
$78k - $156k
...expert to assure successful investigations and corrective actions . Serves as a source of information on the IT Compliance needs and regulatory environment. What You?ll Work On Leads the IT Compliance activities for specific CAPA (Corrective and Preventive Action) event...Worldwide- ...processes. AbbVie is seeking a highly skilled and innovative Principal Research Scientist I to contribute to chemical process... ...the next big win. ~ Author and review technical reports, regulatory documents, patents, and scientific publications, present findings...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...PrincipalWork at officeLocal area
- ...science into life-changing medicines — and we're looking for a Principal Research Engineer I /II to help us push the boundaries of what... .... Champion compliance with AbbVie's safety, quality, and regulatory standards. Qualifications BS (+14 yr experience) MS (+12...PrincipalFull timeLocal area
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Principal Regulatory Affairs Specialist. Be the first to apply!
- food regulatory Waukegan, IL
- regulatory Waukegan, IL
- regulatory contract Waukegan, IL
- regulatory law Waukegan, IL
- compliance technician Waukegan, IL
- customs compliance Waukegan, IL
- legal compliance Waukegan, IL
- director quality assurance regulatory affairs Waukegan, IL
- regulatory affairs assistant Waukegan, IL
- housing compliance Waukegan, IL



