Regulatory Affairs Specialist jobs in Indiana

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 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 Zimmer Biomet product or technology every 8 seconds.


    As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered, and recognized.


    How You'll Create Impact
    • Assist with assembly, distribution, storage, tracking and retrieval of information pertinent to the regulatory process; including the regulatory submissions process.
    • Author and publish electronic submissions.
    • Respond to requests from foreign governments and/or distributors to prepare and submit documentation for marketing approval as well as provide routine regulatory information to associates and affiliates.
    • Assist with research, analysis, and communication of information pertaining to the appropriate regulatory pathway for new or modified products.
    • Provide regulatory direction to development project teams as a core team member; develops regulatory strategy for new products.
    • Evaluate risk of proposed regulatory strategies and offers solutions.
    • Review proposed labeling for compliance with applicable US and international regulations.
    • Write, manage, and approve the development of package inserts.
    • Review, evaluate, and approve promotion and advertising material for compliance with applicable regulations.
    • Review proposed product changes for impact on regulatory status of the product.
    • Follow Zimmer Biomet regulatory affairs policy and procedures.
    • May provide training and/or guidance to entry-level associates, analysts, interns, and specialists.
    • Communicate with regulatory and governmental agencies.
    Your Background

    Requires a Bachelor’s degree in Regulatory Affairs, Engineering, or Life Sciences, or related field.

    Requires 5 years of experience in the job offered or a related role.

    Must have 3 years of experience in orthopaedic or medical device industry.

    Must have 3 years of experience with FDA and EU regulations (including labeling regulations) and regulations outside of the US/EU.

    Must have 2 years of experience working with medical products and advanced anatomic knowledge.

    Must have 2 years of experience with Interpreting and applying FDA regulations to business practices and providing regulatory input, advice, and guidance to the organization and design teams.

    Travel Expectations

    Position permits remote work throughout the U.S. Position requires up to 15% domestic travel.


    EOE/M/F/Vet/Disability

  • Just Posted

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Regulatory Affairs Specialist
  • Actalent
  • Franklin, IN OTHER
  • ****IMMEDIATE OPENING FOR REGULATORY SPECIALIST- ONSITE****This role involves preparing documentation to support international product registration, maintaining registration files and electronic datab...
  • Just Posted

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Regulatory Affairs Specialist - EPA
  • US01 Elanco US Inc.
  • Greenfield, IN FULL_TIME
  • At Elanco (NYSE: ELAN) – it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm anima...
  • 23 Days Ago

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Regulatory Affairs Specialist - Urgently Hiring!
  • Zimmer Biomet
  • Indiana, IN FULL_TIME
  • This job offer is not available in your country. Valued Team member : We are glad you are exploring new opportunities within Zimmer Biomet! How You'll Create Impact Assist with assembly, distribution,...
  • 1 Day Ago

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Quality Assurance and Regulatory Affairs Specialist
  • Red Star
  • Larwill, IN FULL_TIME
  • SUMMARY: The position of QARA Specialist is responsible for planning, directing, and/or coordinating regulatory affairs activities of Red Star Contract Manufacturing to ensure compliance with regulati...
  • 8 Days Ago

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Regulatory Affairs Technical Writer
  • Curium Pharma
  • Noblesville, IN FULL_TIME
  • About Curium Curium is the world’s largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world-class radiopharmaceutical products to ...
  • 19 Days Ago

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Regulatory Affairs Specialist
  • GForce Life Sciences
  • Lake Forest, IL
  • Regulatory Affairs Specialist – Onsite in Lake Forest, IL Must be able to work W2 Summary Our client, a Fortune-500 Medi...
  • 4/26/2024 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...
  • 4/26/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • Highridge Medical
  • Westminster, CO
  • Job Summary: HIGHRIDGE creates the worlds most innovative spinal solutions across the spectrum from Motion Preservation ...
  • 4/26/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • ProKatchers LLC
  • St Louis, MO
  • Job Title: Regulatory Affairs Specialist Location: 63103, St Louis, Missouri, United States Duration: 24 Months Job Desc...
  • 4/25/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • Insight Global
  • Greensboro, NC
  • Location: Greensboro, NC - remote to start, but will transition to a hybrid model in the coming months Contract: 3 month...
  • 4/25/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • Coltene
  • Cuyahoga Falls, OH
  • About the Organization Coltene is a global leader in the development, manufacture and sale of consumables and small-size...
  • 4/25/2024 12:00:00 AM

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Regulatory Affairs Specialist
  • Prokatchers Llc
  • Saint Louis, MO
  • Job Title: Regulatory Affairs Specialist Location: 63103, St Louis, Missouri, United States Duration: 24 Months Job Desc...
  • 4/22/2024 12:00:00 AM

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Regulatory Affairs Specialist II - Electrophysiology
  • Abbott Laboratories
  • Plymouth, MN
  • Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-chan...
  • 2/22/2024 12:00:00 AM

Indiana /ˌɪndiˈænə/ (listen) is a U.S. state located in the Midwestern and Great Lakes regions of North America. Indiana is the 38th largest by area and the 17th most populous of the 50 United States. Its capital and largest city is Indianapolis. Indiana was admitted to the United States as the 19th U.S. state on December 11, 1816. Indiana borders Lake Michigan to the northwest, Michigan to the north, Ohio to the east, Kentucky to the south and southeast, and Illinois to the west. Before becoming a territory, various indigenous peoples and Native Americans inhabited Indiana for thousands of ye...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Regulatory Affairs Specialist jobs
$73,676 to $98,737

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