Regulatory Affairs Specialist jobs in North Carolina

Regulatory Affairs Specialist supports the oversight of regulatory matters and strategy implementation to ensure the organization complies with applicable regulations. Prepares filings and tracks applications for licensing, certification, and permits and interacts with governmental officials during the regulation and certification process. Being a Regulatory Affairs Specialist monitors compliance with existing regulations and upcoming or changing regulations. Performs impact analysis of regulatory changes and produces status reports. Additionally, Regulatory Affairs Specialist participates in processes to report, investigate, and addresses any issues of non-compliance. Typically requires a bachelor's degree. Typically reports to a supervisor or manager. The Regulatory Affairs Specialist occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. To be a Regulatory Affairs Specialist typically requires 2 -4 years of related experience. (Copyright 2024 Salary.com)

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Regulatory Affairs Operations Specialist
  • Merz Therapeutics
  • Raleigh, NC FULL_TIME
  • Based in the Raleigh, NC Corporate office - Hybrid 

    Step into the future with us at Merz Therapeutics, where our family roots meet a bold new vision. Together, we’re embarking on a transformative journey, blending time-honored traditions with exciting new products. 

    As a private, family-owned company, we have the liberty and support to make decisions for ourselves, our customers and the patients we serve. We pride ourselves on building an inclusive culture where there is room to celebrate individual growth with the ability to contribute to a common good as a collaborative team. Our mission is grounded in a long-term view of making a difference for the common good, while growing together as a family. 

    If you‘re looking to immerse yourself in a passionate team rooted in community, connection and camaraderie, then we’re looking for YOU! #IAmMerz 

    Are you ready to galvanize a team around a culture of care, putting patients first to spark change? 

    The Regulatory Operations Specialist will be responsible for the planning, compilation, and publishing of both routine and complex submissions as well as document archiving of Merz products. This role will ensure quality assurance of submission documentation and published output for technical completeness and accuracy. The Regulatory Operations Specialist will maintain familiarity with current regulatory submission standards and industry best practices. They will collaborate with Regulatory Affairs staff and contributing functional areas to assure adequate prioritization and scheduling of regulatory submissions. This role will help with other projects and activities as assigned by management to support the Regulatory Operations function.  

     

    Major duties 

    Description 

    Publishing/Dossier Management 

    Compile, format, and publish regulatory submissions in accordance with electronic Common Technical Document (eCTD) requirements.  

    Publishing/Dossier Management 

    Ensure accuracy and completeness of regulatory submissions, prior to submission to health authorities. 

    Publishing/Dossier Management 

    Collaborate with cross-functional teams to gather necessary information and documents for regulatory submissions and provide guidance and support on publishing requirements and processes.  

    Publishing/Dossier Management 

    Maintain regulatory submission timelines and ensure timely submission of documents to health authorities. 

     

    Publishing/Dossier Management 

    Perform Regulatory Information Management tasks including file transfer, storage, tracking and archival of Regulatory submission documentation, including agency correspondence in a time-sensitive manner  

    Publishing/Dossier Management 

    Assist in the development and implementation of processes to streamline regulatory publishing activities and improve efficiency. 

     

    General Regulatory Duties 

    Stay current with regulatory guidelines and industry best practices related to electronic submissions and regulatory publishing. 

     

     General Regulatory Duties 

    Functions as a change agent that can exhibit regulatory knowledge and awareness, technical competence, sound judgment and a professional demeanor.  

    Regulatory Systems 

    Support in-house training to ensure optimal use of templates, processes, and tools critical for submission documents and information management. 

     

    Education 

    Bachelor’s degree is Preferred​ 

    Degree in Information Management/Information Technology/Biological Sciences is Preferred

     

    Professional experience 

    • Minimum of 3 years pharmaceutical industry experience; preferably within the Regulatory Affairs/Operations function with knowledge of health agency requirements is ​​Required​

    Don’t meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. At Merz Therapeutics we are dedicated to building a diverse, inclusive, and authentic workplace, so if you’re excited about this role but your past experience doesn’t align perfectly with every qualification in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles. 

    Recruitment Note: Merz Therapeutics only sends emails from verified “merz.com” addresses and never asks for sensitive, personal information or money. If you have any doubts about the authenticity of any type of communication from, or on behalf of Merz Therapeutics, please contact Therapeutics.HR@merz.com 

  • 4 Days Ago

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Regulatory Affairs Specialist III
  • Thermo Fisher Scientific
  • Asheville, NC FULL_TIME
  • Do you have a passion for innovative ideas and groundbreaking discoveries? With over $1 billion invested annually in R&D, at Thermo Fisher Scientific you’ll help solve some of the world’s toughest cha...
  • 1 Day Ago

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Regulatory Affairs Specialist III
  • myGwork - LGBTQ+ Business Community
  • Asheville, NC FULL_TIME
  • This inclusive employer is a member of myGwork – the largest global platform for the LGBTQ business community. Job DescriptionDo you have a passion for innovative ideas and groundbreaking discoveries?...
  • 1 Day Ago

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Senior Regulatory Affairs Specialist
  • WorkPath Partners
  • Huntersville, NC OTHER
  • The Senior Regulatory Affairs Specialist will be responsible for ensuring compliance with all regulatory requirements for medical devices and pharmaceutical products.This position requires a deep unde...
  • 12 Days Ago

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Regulatory Affairs Senior Specialist - Medical Devices
  • Career Opportunities at Merz North America
  • Raleigh, NC FULL_TIME
  • The Regulatory Affairs Senior Specialist - Medical Devices coordinates the regulatory activities for development projects including new products and life cycle management. This includes assisting with...
  • 20 Days Ago

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Sr Manager, Regulatory Affairs
  • myGwork - LGBTQ+ Business Community
  • Weaverville, NC FULL_TIME
  • This inclusive employer is a member of myGwork – the largest global platform for the LGBTQ business community. Job DescriptionAs part of the Thermo Fisher Scientific team, you'll discover meaningful w...
  • 2 Days Ago

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Regulatory Affairs Specialist
  • GForce Life Sciences
  • Santa Clara, CA
  • Regulatory Affairs Specialist II – Santa Clara, CA Must be able to work on a W2 Job Summary We're looking for a Regulato...
  • 6/11/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • Experis
  • Maplewood, MN
  • Our client, is seeking a Regulatory Specialist to join their team. As a Regulatory Specialist, you will lead/ coordinate...
  • 6/11/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • Planet Pharma
  • Immediate need for Regulatory Affairs Specialist with a Clinical Research Organization in Raleigh. Hybrid position - wil...
  • 6/10/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • Astrix
  • Fort Worth, TX
  • Exciting 2 year development opportunity to work for a global leader dedicated to helping people see brilliantly. The lar...
  • 6/10/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • Highridge Medical
  • Westminster, CO
  • Job Summary: HIGHRIDGE creates the world’s most innovative spinal solutions across the spectrum from Motion Preservation...
  • 6/9/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • CM Medical Recruitment
  • CM Medical is seeking an experienced regulatory professional to join a fast growing team in the EP/CRM device space. In ...
  • 6/8/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • Baylor College of Medicine
  • Texas City, TX
  • Division: Office of Research Work Arrangement: Onsite only Location: Texas Medical Center, Houston, TX Salary Range: $54...
  • 6/8/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • Net2Source Inc.
  • Palo Alto, CA
  • Job Title: Regulatory Affairs Professional 4 Duration: 12 months (Possible Extension ) Location: Palo Alto CA 94304 (Hyb...
  • 6/7/2024 12:00:00 AM

North Carolina (/ˌkærəˈlaɪnə/ (listen)) is a state in the southeastern region of the United States. It borders South Carolina and Georgia to the south, Tennessee to the west, Virginia to the north, and the Atlantic Ocean to the east. North Carolina is the 28th-most extensive and the 9th-most populous of the U.S. states. The state is divided into 100 counties. The capital is Raleigh, which along with Durham and Chapel Hill is home to the largest research park in the United States (Research Triangle Park). The most populous municipality is Charlotte, which is the second-largest banking center in...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Regulatory Affairs Specialist jobs
$73,292 to $98,219

Regulatory Affairs Specialist in Petaluma, CA
The regulatory affairs industry plays an important role in ensuring the safety of countless products that Americans use every day—from food and beverages to pharmaceuticals and medical devices to electronics and more.
February 02, 2020
Becoming a regulatory affairs specialist is one of the most common ways to break into the industry.
February 10, 2020
Regulatory Affairs Specialist in Boulder, CO
They often advise project teams on subjects such as premarket regulatory requirements, export and labeling requirements, or clinical study compliance issues.
February 03, 2020
Regulatory Affairs Specialist in Concord, NH
Are you working as a Regulatory Affairs Specialist? Help us rate Regulatory Affairs Specialist as a Career.
December 31, 2019