Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Principal Regulatory Affairs Specialist

$80.9k - $127.05k

Cardinal Health

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. Location The ideal candidate will reside within a reasonable commuting distance of one of our office locations: Waukegan, IL or El Paso, TX Schedule Hybrid. 1-2x a week in office. Job Summary The Principal Regulatory Affairs Specialist will support the Medical Solutions Regulatory affairs team. They are responsible for regulatory activities associated with convenience kitting (Presource® kitting). This includes being regulatory lead for strategy, 510ks, and FDA regulations for the kitting products. 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. 5-7 years regulatory affairs experience preferred. Experience in medical device industry a plus. Proficiency in US FDA 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 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. Equal Employment Opportunity Statement 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. Candidates who are back‑to‑work, people with disabilities, without a college degree, and Veterans are encouraged to apply. #J-18808-Ljbffr Cardinal Health

Vacancy posted 4 days ago
Similar jobs that could be interesting for youBased on the Principal Regulatory Affairs Specialist in Waukegan, IL vacancy
  • What Regulatory Affairs contributes to Cardinal HealthRegulatory provides regulatory affairs and product development consulting...  ...: Hybrid. 1-2x a week in office.Job SummaryThe Principal Regulatory Affairs Specialist will support the Medical Solutions Regulatory affairs... 
    Principal
    Full time
    Temporary work
    Work experience placement
    Work at office
    Local area
    Immediate start

    Cardinal Health

    Waukegan, IL
    1 day ago
  •  ...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... 
    Suggested
    Full time

    Uline Shipping Supplies

    Waukegan, IL
    3 days ago
  • $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 OnLeads the IT Compliance activities for specific CAPA (Corrective and Preventive Action) event... 
    Suggested
    Worldwide

    Abbott

    Waukegan, IL
    4 days ago
  •  ...and fostering collaborative school environments where staff can make a meaningful impact. Role Description The Elementary Assistant Principal is a full-time, on-site role based in Waukegan, IL. This position supports the Principal in leading the school's academic and... 
    Principal
    Full time

    Waukegan Community Unit District 60

    Waukegan, IL
    1 day ago
  •  ...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... 
    Principal
    Work at office

    Katalyst Healthcares and Life Sciences

    Waukegan, IL
    4 days ago
  •  ...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.... 
    Principal
    Full time
    Work experience placement
    Local area
    Worldwide

    AbbVie Inc.

    North Chicago, IL
    a month ago
  •  ...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... 
    Principal
    Full time
    Local area

    AbbVie Inc.

    North Chicago, IL
    more than 2 months ago
  •  ...development of AbbVie’s clinical candidates. We are seeking a Principal Research Scientist II to lead the Radiochemistry team that is...  ...troubleshooting strategic and experimental issues. Author and review key regulatory documents, laboratory data, technical memos, standard... 
    Principal
    Work experience placement

    Allergan

    North Chicago, IL
    1 day ago
  •  ...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... 
    Principal
    Full time
    Temporary work
    Work experience placement
    Local area

    AbbVie Inc.

    North Chicago, IL
    more than 2 months ago
  •  ...more information about AbbVie, please visit Job Description The Principal Quality Engineer – DevOps is responsible for ensuring that...  ...operations and software lifecycle processes fully comply with regulatory requirements and corporate standards. This role provides leadership... 
    Principal

    AbbVie

    North Chicago, IL
    4 days ago
  •  ...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... 
    Principal
    Full time
    Local area

    AbbVie Inc.

    North Chicago, IL
    19 days ago
  • 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...
    Principal
    Full time
    Local area

    AbbVie Inc.

    North Chicago, IL
    more than 2 months ago
  •  ...onLinkedIn,Facebook,Instagram,XandYouTube. Job Description The Principal Data Scientist will serve as a strategic leader and technical...  ...ML workflow integration that ensure consistency, quality, and regulatory compliance Advanced AI/ML Solution Architecture Oversee the development... 
    Principal

    BioSpace, Inc.

    North Chicago, IL
    1 day ago
  •  ...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... 
    Principal
    Full time
    Work experience placement
    Local area

    AbbVie Inc.

    North Chicago, IL
    8 days ago
  • 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...
    Principal
    Full time
    Local area

    AbbVie Inc.

    North Chicago, IL
    25 days ago
  •  ...Responsibilities Support regional Regulatory Information Management (RIM) activities using systems such as COSMOS, HUBBLE, and CIU. Create...  ...initiatives. Requirements Bachelor's degree in Regulatory Affairs, Pharmacy, Health Sciences, or a related discipline. Experience... 

    Katalyst CRO

    North Chicago, IL
    5 days ago
  •  ...ICU Medical is seeking a Regulatory Affairs professional to support global and US registrations of medical device products. You will analyze regulatory requirements, create and maintain registration dossiers, and ensure compliance across submissions and change management... 

    ICU Medical

    Lake Forest, IL
    1 day ago
  • $109.5k

     ...assignments related to a specific technical field or discipline. A Principal Engineer has full knowledge of other related disciplines...  ...the design solutions for novel or complex problems; integrates regulatory and operational needs; assesses cost benefit. Explores multiple... 
    Principal
    Local area

    AbbVie

    North Chicago, IL
    2 days ago
  • 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...
    Principal
    Full time
    Local area

    AbbVie Inc.

    North Chicago, IL
    more than 2 months ago
  •  ...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... 
    Principal
    Full time
    Local area

    AbbVie Inc.

    North Chicago, IL
    a month ago
  • Job-ID29031369Reference26-22116Purpose: Describe the primary goals, objectives or functions or outputs of this position. Assure compliance with FDA current Good manufacturing Practices (cGMP) and Good Distribution Practices (cGDP) regulations. Assure compliance with Corporate...

    Mindlance

    North Chicago, IL
    1 day ago
  •  ...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... 
    Principal
    Full time
    Local area

    AbbVie

    North Chicago, IL
    2 days ago
  •  ...organization is seeking a highly motivated, talented, and creative Principal Research Scientist II to be a key contributor for our Process...  ..., process development.  Profound knowledge of quality and regulatory requirements for processing and filling equipment for... 
    Principal
    Full time
    Local area

    AbbVie

    North Chicago, IL
    16 days ago
  •  ...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... 
    Principal
    Full time
    Work at office
    Local area

    AbbVie

    North Chicago, IL
    6 days ago
  •  ...and resolution of technical manufacturing issues in a commercial setting. Effective cross functional interactions with quality and regulatory functions and on-site manufacturing personnel is key for successful job performance. The Peptide Process Engineer will research... 
    Principal
    Full time
    Temporary work
    Work experience placement
    Local area

    AbbVie

    North Chicago, IL
    27 days ago
  •  ...interactions with other functions (e.g., technical, quality, regulatory) and on-site manufacturing personnel are key for successful job...  ...radioactive compounds, and GxP compliance.  Effectively function as a principal investigator, generating original technical ideas and research... 
    Principal
    Local area

    AbbVie

    North Chicago, IL
    19 days ago
  • 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...
    Principal
    Full time
    Local area

    AbbVie Inc.

    North Chicago, IL
    a month ago
  • $68k - $136k

     ...medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries. Regulatory Affairs Specialist II Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be... 
    Work experience placement
    Worldwide

    Abbott

    Lake Forest, IL
    2 days ago
  • USG is seeking a senior building codes and fire rated systems professional to serve as a practical, externally credible subject matter expert for building code interpretation, codes and standards development, and complex customer/jobsite issue resolution.This role is part...
    Principal
    Hourly pay
    For contractors

    USG corporation

    Libertyville, IL
    3 days ago
  •  ...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.... 
    Principal
    Full time
    Local area
    Worldwide

    AbbVie

    North Chicago, IL
    1 day ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Principal Regulatory Affairs Specialist. Be the first to apply!