Jobs
>
Winnetka

    Associate Regulatory Affairs Specialist - Winnetka, United States - Medline Industries

    Medline Industries
    Medline Industries Winnetka, United States

    4 weeks ago

    Default job background
    Description
    JOB SUMMARY:

    Under direct supervision, responsible for executing global regulatory activities necessary to obtain and maintain global regulatory approvals. Prepare and review documents for regulatory filings for regulatory authorities under general supervision of RA management. Participate in teams within the department and organization by bringing basic technical skills, critical thinking, and understanding of related regulatory frame-works to meet short-term regulatory goals and business requests.

    MAJOR RESPONSIBILITIES:
    • Investigate federal, state or local licensing requirements through review of laws and regulations or through direct contact with regulatory authorities.
    • In support of business priorities, determine the requirements for marketing and distributing regulated products
    • Communicate appropriate regulatory requirements to internal or external customers or vendors where necessary.
    • Review, identify and assess documentation provided by product managers, vendors, divisional QA's and marketing (internal and external customers) to ensure it meets applicable regulatory requirements.
    • Interact with internal and external customers to complete the proper licensing, registration, listing, or submission for Medline products and/or facilities.
    • Partner with team members, internal customers, external suppliers, and consultants to complete assigned regulatory activities.
    Education
    • B.A. or B.S. degree in life science field (biology, microbiology, chemistry, etc.), engineering, medical technology, regulatory science, or related.


  • Medline Winnetka, United States

    JOB SUMMARY: · Under general supervision, the Regulatory Specialist is responsible for planning and executing global regulatory activities necessary to obtain and maintain global regulatory approvals. Prepare comprehensive regulatory strategies for new devices, new launch markets ...


  • Medline Industries Winnetka, United States

    JOB SUMMARY: · Under general supervision, the Regulatory Specialist is responsible for planning and executing global regulatory activities necessary to obtain and maintain global regulatory approvals. Prepare comprehensive regulatory strategies for new devices, new launch market ...


  • Medline Winnetka, United States

    JOB SUMMARY: · Under general supervision, the Regulatory Specialist is responsible for planning and executing global regulatory activities necessary to obtain and maintain global regulatory approvals. Prepare comprehensive regulatory strategies for new devices, new launch market ...


  • Medline Industries Winnetka, United States

    JOB SUMMARY: · Remote work eligible except in Colorado and Connecticut. · Under limited supervision, the Senior Regulatory Specialist is responsible for planning and executing critical and complex global regulatory projects necessary to obtain and maintain global regulatory app ...


  • Medline Industries Winnetka, United States

    JOB SUMMARY: · Under direct supervision, responsible for executing global regulatory activities necessary to obtain and maintain global regulatory approvals. Prepare and review documents for regulatory filings for regulatory authorities under general supervision of RA management ...


  • Medline Industries Winnetka, United States

    JOB SUMMARY: · Under general supervision, the Regulatory Specialist is responsible for planning and executing global regulatory activities necessary to obtain and maintain global regulatory approvals. Prepare comprehensive regulatory strategies for new devices, new launch market ...


  • ACL Digital Niles, United States

    THE OPPORTUNITY: · We are seeking a highly motivated and detail-oriented individual to join our team as a Regulatory Affairs Specialist for a 9 month contract. We are seeking an experienced individual with a strong background in the medical device industry and extensive knowledg ...


  • Medline Industries Winnetka, United States

    JOB SUMMARY: · Under direct supervision, responsible for executing global regulatory activities necessary to obtain and maintain global regulatory approvals. Prepare and review documents for regulatory filings for regulatory authorities under general supervision of RA management ...


  • GForce Life Sciences Lake Forest, United States

    The position of Regulatory Affairs Specialist II is within our client's Infectious Disease business unit. In this role, you will prepare documentation for EU Technical Files and international product registrations. · TERM & START · 1-year contract starting 6/10/24 with possibili ...


  • Northwestern Memorial Healthcare Chicago, United States Full time

    Job Description · The Regulatory Affairs Specialist reflects the mission, vision, and values of NM, adheres to the organization's Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accredit ...


  • Katalyst HealthCares & Life Sciences North Chicago, United States

    Responsibilities: Prepares robust regulatory applications (either for FDA or for international regulatory agencies) to achieve departmental and organizational objectives. · Creates, reviews, and approves engineering changes. · Acts as core team member providing review and analys ...


  • Metropolitan Water Reclamation District of Greater Chicago Chicago, United States

    General Statement · Under direction, performs a variety of public information assignments including developing and writing press releases, talking points, presentations, fact sheets, and social media messages, and graphic design. · Essential Job Functions · Essential job functi ...


  • McCain Foods Villa Park, United States

    Position Title: Regulatory Affairs Specialist · Position Type: Regular - Full-Time · Position Location: Oakbrook Terrace · Requisition ID: 28326 · The Regulatory Affairs Specialist is responsible for product composition and label regulatory compliance for finished goods manuf ...


  • IMS People Round Lake, United States

    Job Description · Job DescriptionTitle: Regulatory Affairs Ops Specialist II · Location: 25212 W. Illinois Route 120, Round Lake, IL 60073 · Duration: 5 Months contract with possible extension · Description: · Summary: · Responsible for the implementation of complex global regula ...


  • Office of the Illinois State Treasurer Chicago, United States

    JOB OPPORTUNITY ANNOUNCEMENT · Position Title: Community Affairs Specialist · Division: Civic Engagement · Union: Teamsters Local 916 · Location: Chicago, Illinois · Salary: $ 50,000 Annually · Position Summary: · Responsible for developing marketing initiatives and making presen ...


  • Office of the Illinois State Treasurer Chicago, United States

    Job Description · Job DescriptionJOB OPPORTUNITY ANNOUNCEMENT · Position Title: Community Affairs Specialist · Division: Civic Engagement · Union: Teamsters Local 916 · Location: Chicago, Illinois · Salary: $50,000 Annually · Position Summary: · Responsible for developing mark ...


  • McCain Foods Oakbrook Terrace, United States

    Position Title: · Regulatory Affairs Specialist · Position Type: · Regular - Full-Time · Position Location: · Toronto HQ · Requisition ID: · 28326 · The Regulatory Affairs Specialist is responsible for product composition and label regulatory compliance for finished goods ...


  • Abbott Des Plaines, United States

    Job Description · Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and bra ...


  • Northwestern Memorial Healthcare Chicago, United States

    Job Description · The Regulatory Affairs Specialist reflects the mission, vision, and values of NM, adheres to the organizations Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accredit ...


  • Abbott Green Oaks, United States

    The Opportunity · This position is field based and remote to candidates located in the United States. Candidates must be willing to travel up to 50%. · We are seeking an experienced, high caliber Senior Field Clinical Specialist. This position will be primarily responsible for ...