Regulatory Affairs Manager jobs in Colorado

Regulatory Affairs Manager manages regulatory matters and executes the strategy to ensure the organization complies with applicable regulations. Implements processes and systems to ensure that all necessary licensing, filings, certifications, and permits are processed and monitored. Being a Regulatory Affairs Manager utilizes established monitoring policies and procedures to ensure compliance with existing regulations. Anticipates new or changing regulations and coordinates with internal stakeholders to develop strategies to address changes in product, operations, or testing requirements. Additionally, Regulatory Affairs Manager investigates and addresses any reported issues of non-compliance. Requires a bachelor's degree. Typically reports to a director. The Regulatory Affairs Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. To be a Regulatory Affairs Manager typically requires 5 years experience in the related area as an individual contributor. 1 - 3 years supervisory experience may be required. Extensive knowledge of the function and department processes. (Copyright 2024 Salary.com)

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Regulatory Affairs Project Manager
  • RapidAI
  • Golden, CO FULL_TIME
  • RapidAI is the global leader in using AI to combat life-threatening vascular and neurovascular conditions. RapidAI is empowering physicians to make faster decisions for better patient outcomes, leading the next evolution of clinical decision-making and patient workflow. Based on intelligence gained from over 10 million scans in more than 2,000 hospitals in over 60 countries, the Rapid® platform transforms care coordination, offering care teams a level of patient visibility never before possible. RapidAI – where AI meets patient care.


    At RapidAI, we believe in leveraging cutting-edge technology and research to impact millions of lives. Our software products enhance doctors’ capabilities across hospitals worldwide to respond to and make the best decisions for patients quickly. We are looking for a high-energy employee who is excited to be at the forefront medical device software development. The successful candidate will meet the criteria defined below, and in doing so, will help deliver the best patient care to patients all around the world.

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    What you will do:
    • Assemble, distribute, store, track and retrieve information pertinent to the regulatory process, including the regulatory submissions process  
    • Author and publish electronic submissions
    • Manage requests from foreign government and/or distributors as needed
    • Research, analyze and communicate information pertaining to the appropriate regulatory pathway for new or modified products
    • Provide regulatory direction to development project teams as a core team member; helps develop regulatory strategy for new products
    • Evaluate risk of proposed regulatory strategies; may offer solutions
    • Review proposed labeling for compliance with applicable global regulations
    • Review and evaluate promotion and advertising material for compliance with applicable regulations
    • Review proposed product changes for impact on regulatory status of the product
    • Communicate with regulatory and governmental agencies
    • Labeling and promotion materials review
    • Apply FDA regulations to business practices and provides regulatory input, advice and guidance to design teams
    • Assist quality team – including but not limited to training and document control
    • Work with external RA partners to maintain and update foreign registrations
    • This position does not have direct reports.
    • Perform any other related activities assigned by reporting manager.


    What you bring:
    • Strong written/verbal communication and interpersonal skills
    • Strong attention to detail; ability to multi-task and balance competing priorities
    • Knowledge of overall business environment, the SaMD industry, and the marketplace
    • Ability to learn and stay abreast of regulations pertinent to medical devices
    • Ability to building relationships between Regulatory Affairs and other areas of the organization: ability to communicate effectively at all levels
    • Knowledge of FDA, EU, and other regulatory body regulations


    What we offer you:
    • RapidAI pays 100% for employee coverage & 75% for your dependent coverage for medical, dental & vision premiums.
    • Medical Benefits – We offer a range of policies through TriNet 
    • Life Insurance/AD&D is 1X times your annual salary
    • We pay 100% for Short and Long Term Disability.
    • Healthcare and Dependent care flexible spending accounts are available
    • A 401k plan is offered through Empower
    • RapidAI provides $100 a month for internet/cell/phone services.
    Time Off:
    • We have 10 company paid holidays!
    • RapidAI has a flexible vacation policy.  We urge employees to take vacation! Vacation allows employees to renew, reinvigorate, and rejuvenate.
    Other Cool Benefits:
    • Equity - Stock Options
    • Incentive Compensation
    • And most importantly - You are joining an awesome team!


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    Compensation - The salary range target for the role described in this job description is $99,000 to $110,00. Final offer amounts depend on multiple factors including but not limited to candidate experience and expertise, geographic location, compensation/equity mix, and market data. This position may also be eligible for additional incentives such as equity awards, short-term incentives, or sales compensation.


    RapidAI is committed to creating an inclusive and diverse workplace. We provide equal employment opportunities to all employees and applicants and prohibit discrimination and harassment of any type in regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.


    Please review our CPRA policies here.

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  • 4 Days Ago

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R&D Regulatory Affairs Manager
  • 24 Seven Talent
  • Englewood, CO FULL_TIME
  • Job title: R&D Regulatory Affairs ManagerContract type:Location: EnglewoodDiscipline:Remote: NoSalary: $80,000/year - $120,000/yearReference: 462836Contact name: Nora GillernJob DescriptionOur client ...
  • 15 Days Ago

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Manager, Quality Assurance & Regulatory Affairs - Englewood, CO
  • Getinge
  • Denver, CO FULL_TIME
  • At Getinge we have the passion to perform Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge, our passion is to secure t...
  • 1 Month Ago

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Senior Regulatory Affairs Specialist
  • Eurofins Agroscience Services
  • Centennial, CO FULL_TIME
  • Company DescriptionEurofins Scientific is an international life sciences company, which provides a unique range of analytical testing services to clients across multiple industries. The Group believes...
  • 5 Days Ago

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VP Government and Regulatory Affairs
  • UCHealth
  • Aurora, CO FULL_TIME
  • The Opportunity Vice President, Government & Regulatory Affairs The Vice President Government & Regulatory Affairs develops, directs, executes, and manages UCHealth's strategic and day-to-day relation...
  • 7 Days Ago

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Regulatory Affairs Specialist
  • Highridge Medical
  • Westminster, CO FULL_TIME
  • Job Summary:HIGHRIDGE creates the world’s most innovative spinal solutions across the spectrum from Motion Preservation to MIS to Bone Healing to Core Spine. Working at HIGHRIDGE is not just work. Lif...
  • 7 Days Ago

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Regulatory Affairs Manager
  • Dental Technologies Inc
  • Lincolnwood, IL
  • Job Description Job Description Job Title: Regulatory Affairs Manager Department: Quality Assurance Reports To: Vice Pre...
  • 6/11/2024 12:00:00 AM

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Regulatory Affairs Manager
  • Catalyst Life Sciences
  • Chicago, IL
  • Opportunity to join a global diagnostics company at their HQ just outside of Chicago, focused on the strategy for existi...
  • 6/10/2024 12:00:00 AM

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Regulatory Affairs Manager
  • Blueroot Health™
  • PURPOSE STATEMENT: This position will be responsible for managing and coordinating implementation of regulatory requirem...
  • 6/10/2024 12:00:00 AM

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Regulatory Affairs Manager
  • Lumicity
  • This opportunity is with a company revolutionizing the medical device industry with its cutting-edge technologies and co...
  • 6/9/2024 12:00:00 AM

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Regulatory Affairs Manager
  • Tandym Group
  • Stamford, CT
  • Top hospital in Fairfield county, CT, just over the border from Westchester county NY, is seeking an experienced Regulat...
  • 6/8/2024 12:00:00 AM

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Regulatory Affairs Manager
  • Mastech Digital
  • Oakland, CA
  • Position: HIM Director-Regulatory Affairs Manager Location: Oakland CA USA 94612 (5 days onsite) Duration: 12+ Months (P...
  • 6/7/2024 12:00:00 AM

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Regulatory Affairs Manager
  • SS White Dental
  • Lakewood, NJ
  • SS White Dental is seeking a Senior Regulatory Affairs Manager to support our Regulatory team. Candidates should have a ...
  • 6/7/2024 12:00:00 AM

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Regulatory Affairs Manager
  • Procter & Gamble
  • Reading, England
  • Job Location Reading Job Description P&G is a leading global consumer goods company whose winning brands are Procter & G...
  • 5/22/2024 12:00:00 AM

Colorado (/ˌkɒləˈrædoʊ, -ˈrɑːdoʊ/ (listen), other variants) is a state of the Western United States encompassing most of the southern Rocky Mountains as well as the northeastern portion of the Colorado Plateau and the western edge of the Great Plains. It is the 8th most extensive and 21st most populous U.S. state. The estimated population of Colorado was 5,695,564 on July 1, 2018, an increase of 13.25% since the 2010 United States Census. The state was named for the Colorado River, which early Spanish explorers named the Río Colorado for the ruddy silt the river carried from the mountains. The...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Regulatory Affairs Manager jobs
$141,237 to $199,217

Regulatory Affairs Manager in Wichita Falls, TX
Other names for this job might include Clinical Trials Systems Administrator, Global Regulatory Affairs Manager, Regulatory Administrator, Regulatory Affairs Director, Regulatory Affairs Manager, Regulatory Affairs Portfolio Leader, Regulatory Consultant, Regulatory Leader, Regulatory Process Manager, Regulatory Product Manager.
January 17, 2020
Regulatory Affairs Manager in Baltimore, MD
Lead strategic contributions and initiatives to develop regulatory services and improve current processes and procedures.
January 18, 2020
Regulatory Affairs Manager in Fort Lauderdale, FL
Regulatory Domain Support for business development, including solutioning and developing innovative solutions, creation of materials for and participation in sales pursuits, key client meetings, bid defences for RFIs and RFPs.
December 04, 2019