Regulatory Relations Specialist jobs in Elkhart, IN

Regulatory Relations Specialist files applications and interacts with governmental officials during the regulation and certification process for a plant or other facility. Assists in developing procedures to ensure regulatory compliance. Being a Regulatory Relations Specialist gathers data pertaining to organizational projects and their impact on the regulation process. May require a bachelor's degree. Additionally, Regulatory Relations Specialist typically reports to a supervisor or manager. To be a Regulatory Relations Specialist typically requires 4 to 7 years of related experience. Contributes to moderately complex aspects of a project. Work is generally independent and collaborative in nature. (Copyright 2024 Salary.com)

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Regulatory specialist
  • OrthoPediatrics
  • Warsaw, IN FULL_TIME
  • GENERAL SUMMARY : This position is responsible for managing medical device labeling projects and workstreams (including, but not limited to product labels, package inserts / IFUs, patient cards, translations, labeling systems, GS1 / GTIN, GMDN and UDI initiatives) as necessary to market OrthoPediatrics products in compliance with applicable global regulations and standards.

    It requires a broad understanding of medical device regulations (ex. US, EU, Canada, Australia), label and IFU development, change management systems / procedures / concepts, and labeling systems.

    This position must have the ability to work effectively and efficiently with all team members, have a good understanding of global labeling regulations and requirements.

    Strong attention to detail, written and oral communication, teamwork, and organizational skills are essential, as well as an understanding of Orthopediatrics products and their use.

    This position will also provide support during internal and external audits and reviews. Prior experience is a plus.

    ESSENTIAL FUNCTIONS :

    • Serve as the labeling SME within the company under the direction of the RA Director or designee
    • Work with Regulatory, Development, Quality, Operations and IT to develop / create labeling that complies with global and UDI labeling regulations and requirements, as required
    • Serve as the lead team member for labeling initiatives, including but not limited to :
    • new product development, maintenance projects, and UDI tasks associated with product labels, package inserts / eIFUs, and patient cards
    • Initiate change requests for new and revised labeling; create, maintain, and implement compliant labeling, review product labeling against indicated content, and approve / release labeling documentation for label system usage
    • Coordinate effectively with vendors and suppliers of services (e.g., translation vendors, eIFU hosting, UDI systems (ex.

    GUDID, EUDAMED), instrument and / or implant suppliers) to ensure high quality and accuracy of content

    SUPERVISORY RESPONSIBILITIES : There are no supervisor responsibilities with this position.

    QUALIFICATIONS : To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.

    The requirements listed below are representative of the knowledge, skill and / or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)

    • Ability to build strong relationships, work effectively and efficiently with cross functional team members to create and implement labeling changes
    • Proficient in the use of labeling software (ex. Prisym, Loftware, ROBAR, IQVIA, InDesign, Qarad)
    • Knowledge and solid understanding of global labeling regulations and requirements, and a commitment to learn and stay abreast of medical devices regulations
    • An understanding of orthopedic / medical devices and their use relating to labeling, design change control, and document control and management
    • Must have excellent written and oral communication and technical writing skills.
    • Must be analytical and able to solve problems.
    • Must possess exceptional attention to detail, organization, and multi-tasking skills.
    • Demonstration of strong problem-solving skills; able to analyze all aspects of a situation, identify potential solutions, and implement the best solution in a timely manner

    EDUCATION AND / OR EXPERIENCE : Requires a bachelor’s degree in a technical area with a minimum of 1 year of experience in a labeling capacity, or 2 years of equivalent experience in a related regulatory role in a device industry.

    LANGUAGE SKILLS : Ability to read and comprehend instructions, correspondence, and memos. Ability to prepare routine reports and correspondence.

    Ability to communicate effectively with customers, vendors and other employees of the organization. Requires excellent grammar and spelling.

    Mathematical Skills : Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.

    Reasoning Ability : Ability to carry out instructions furnished in written, oral, or diagram form. Ability to use critical thinking to deal with problems involving multiple variables in a variety of situations.

    Certificates, Licenses, Registrations : Requires a valid driver’s license.

    Other Skills and Abilities : Requires the ability to operate a variety of standard office equipment, such as a computer and keyboard, calculator, fax, photocopier, telephone, cell phone, etc.

    Requires proficiency with Must be fluent in MS Office (Microsoft Word, Excel, Outlook and PowerPoint).

    physical demands : (The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

    Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)

    While performing the duties of this job, the employee is regularly required to sit and use hands to finger handle or feel .

    The employee is frequently required to climb stairs, talk and hear. The employee is occasionally required to stand; walk;

    reach with hands and arms; and stoop, kneel, crouch , or crawl . The employee must occasionally lift and / or move up to 25 pounds.

    Work Environment : ( The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.

    Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)

    The noise level in the work environment is that found in a normal office environment; noise levels during visits to other locations in the building may be moderate and occasionally loud.

    The employee will be required to travel 25% of the time.

    The above statement reflects the general details necessary to describe the principle functions of the occupation described and shall not be construed as a detailed description of all the work requirements that may be inherent in the occupation.

    Last updated : 2024-04-23

  • 1 Day Ago

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Regulatory Affairs Specialist
  • Zimmer Biomet
  • Warsaw, IN FULL_TIME
  • At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a ...
  • 1 Day Ago

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Client Relations Specialist
  • The Shyft Group USA, Inc
  • Bristol, IN FULL_TIME
  • Client Relations Specialist | Utilimaster | Bristol, IN (Main) Regular Employee | Salary Non-Exempt Who we are At The Shyft Group we are driven to deliver, and as the North American leader in specialt...
  • 22 Days Ago

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CPS and Foster Care - Services Specialist 9-12 - Cass
  • CPS and Foster Care - Services Specialist 9-12 -...
  • Cassopolis, MI FULL_TIME
  • Salary $49,795.20 - $81,931.20 Annually Location Cassopolis, MI Job Type Permanent Full Time Job Number SS - CASS Department Health and Human Services - Counties Opening Date 06/08/2023 Bargaining Uni...
  • Just Posted

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Part Time Regulatory Compliance Administrator
  • Instrumedical Technologies, Inc.
  • Warsaw, IN PART_TIME
  • Company Overview:Instru-Med is a leading contract manufacturer operating in accordance with ISO 13485 standards. We specialize in providing high-quality manufacturing solutions for medical devices. Ou...
  • 1 Month Ago

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Leasing and Tenant Relations Coordinator
  • Property Management Services
  • Goshen, IN FULL_TIME
  • Join Our Team as a Leasing and Tenant Relations Manager! Are you a people person with a passion for real estate and love helping people? Do you thrive in a fast-paced environment where no two days are...
  • Just Posted

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0 Regulatory Relations Specialist jobs found in Elkhart, IN area

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Regulatory Specialist - Labeling
  • Orthopediatrics
  • Warsaw, IN
  • GENERAL SUMMARY:This position is responsible for managing medical device labeling projects and workstreams (including, b...
  • 4/26/2024 12:00:00 AM

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Medical Receptionist
  • Beacon Health System
  • Elkhart, IN
  • Full-time 500 Arcade Avenue Clerical Day $1,000 USD SIGNING BONUS Reports to the Practice Manager and works under the di...
  • 4/26/2024 12:00:00 AM

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Senior Security Analyst
  • Lippert
  • Elkhart, IN
  • Overview: Who We Are: Lippert is a leading, global manufacturer and supplier of highly engineered products and customize...
  • 4/26/2024 12:00:00 AM

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Chef
  • Enlivant
  • Elkhart, IN
  • ** Chef** **Job Category****:** Dining **Requisition Number****:** COOKC08624 Showing 1 location **Job Details** **Descr...
  • 4/26/2024 12:00:00 AM

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Director of Infosec & Compliance
  • Lippert Components Inc.
  • Elkhart, IN
  • OverviewWho We Are:Lippert is a leading, global manufacturer and supplier of highly engineered products and customized s...
  • 4/24/2024 12:00:00 AM

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Regulatory Specialist - Labeling
  • OrthoPediatrics
  • Warsaw, IN
  • GENERAL SUMMARY:This position is responsible for managing medical device labeling projects and workstreams (including, b...
  • 4/23/2024 12:00:00 AM

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Environmental, Health & Safety Manager
  • Nibco Inc
  • Elkhart, IN
  • NIBCO is a recognized leader in the flow control industry. Headquartered in Northern Indiana, with a manufacturing histo...
  • 4/22/2024 12:00:00 AM

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Support Services Coordinator (QIDP)
  • Mosaic
  • Osceola, IN
  • If making a positive impact in the lives of others is a constant on your to-do list -- you'll LOVE working with a team t...
  • 3/21/2024 12:00:00 AM

Elkhart /ˈɛlkɑːrt/ is a city in Elkhart County, Indiana, United States. The city is located 15 miles (24 km) east of South Bend, Indiana, 110 miles (180 km) east of Chicago, Illinois, and 150 miles (240 km) north of Indianapolis, Indiana. Elkhart has the larger population of the two principal cities of the Elkhart-Goshen Metropolitan Statistical Area, which in turn is part of the South Bend-Elkhart-Mishawaka Combined Statistical Area, in a region commonly known as Michiana. The population was 50,949 at the 2010 census. Despite the shared name, it is not the county seat of Elkhart County; that ...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Regulatory Relations Specialist jobs
$71,112 to $97,625
Elkhart, Indiana area prices
were up 1.3% from a year ago

Regulatory Relations Specialist in Albany, GA
The Regulatory Relations Specialist is responsible for the execution of the overall strategy for regulatory engagement and enterprise-wide standards.  This includes assisting with the management of regulatory examinations, inquiries and meetings.  Additional responsibilities include.
December 09, 2019
Regulatory Relations Specialist in Monroe, LA
We are looking for a Marketing Specialist to plan, coordinate and manage marketing campaigns and activities across marketing channels.
February 06, 2020