Regulatory Affairs Manager jobs in District of Columbia

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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Manager Regulatory Affairs
  • Philip Morris International
  • Washington, DC FULL_TIME
  • Be a part of a revolutionary change

    At PMI, we’ve chosen to do something incredible. We’re totally transforming our business and building our future on one clear purpose – to deliver a smoke-free future.

    In late 2022, PMI acquired Swedish Match and its leading oral nicotine product portfolio. We can now provide legal age nicotine users who would otherwise continue to smoke, access to a broader range of better alternatives to combustible products.

    With huge change, comes huge opportunity. So, wherever you join us, you’ll enjoy the freedom to dream up and deliver better, brighter solutions and the space to move your career forward in endlessly different directions.

    Our success depends on people who are committed to our purpose and have an appetite for progress.

    Your ‘day to day’:

    1. Manages regulatory submission development & assembly
    • Coordinates communication across multifunctional submission preparation teams to ensure that all parties are aligned
    • Manages project timeline, include tasks, responsible parties, and target completion dates
    • Identifies any issues that present risk to submission readiness in a timely manner and facilitates resolution of issues by appropriate parties
    • Manages TPSAC preparation activities
    • Develops documentation of steps to assemble marketing applications & other FDA submissions and identifies changes to streamline & expedite the process
    2. Serve as key writer for regulatory submissions
    • Identifies opportunities to create submissions likely to receive FDA authorization
    • Helps develop framing of submissions narratives (storyboards)
    • Serves as the primary author for drafting submission executive summaries
    • Helps to ensure that each module is written such that the full assembled submission is integrated to support the narrative

    3. Monitors & facilitates internal & external activities related to regulatory submissions
    • Monitors research being conducted for regulatory submissions
    • Identifies any issues with research that may negatively impact regulatory submission content and timeline
    • Liaises with US Commercial to ensure regulatory needs are being met
    • Networks with external stakeholders interested in regulatory submissions

    Who we’re looking for:

    • Advanced degree in a scientific or medical field
    • 5 or more years of related public health and industry work experience
    • Knowledge of tobacco science
    • Ability to collaborate cross-functionally in a matrixed organization
    • Demonstrated ability to influence peers and organizational leadership on significant policy decisions
    • Experience communicating orally and in writing to a variety of audiences (e.g., scientists, clinicians, lawyers, government officials, and businesspersons)
    • Reputation for ethical conduct and unquestionable integrity
    • Strong interpersonal and networking skills
    • Demonstrated creative and strategic thinking

    It is preferred that the person holding this position have the following qualifications:

    • 3 or more years of experience at FDA’s Center for Tobacco Products
    • 3 or more years of experience at tobacco manufacturer or related organization
    • Thorough understanding of FDA regulatory processes for tobacco products
    • Relationships with a wide range of stakeholders at tobacco government agencies, NGOs, and product manufacturers

    What we offer

    • We offer a competitive base salary, annual bonus (applicable based on level of position), great medical, dental and vision coverage, 401k with a generous company match, incredible wellness benefits, commuter benefits, pet insurance, generous PTO, and much more!
    • We have implemented Smart Work, a hybrid model of working that promotes flexibility in the workplace.
    • Seize the freedom to define your future and ours. We’ll empower you to take risks, experiment and explore.
    • Be part of an inclusive, diverse culture where everyone’s contribution is respected; Collaborate with some of the world’s best people and feel like you belong.
    • Pursue your ambitions and develop your skills with a global business – our staggering size and scale provides endless opportunities to progress.
    • Take pride in delivering our promise to society: To improve the lives of a billion smokers.

    Annual Base Salary Range: $148,000-$203,500

    PMI is an Equal Opportunity Employer

    PMI Global Services Inc. and PM Global Brands Inc. are a subsidiary of Philip Morris International Inc. Philip Morris International (PMI) is leading a transformation in the tobacco industry to create a smoke-free future and ultimately replace cigarettes with smoke-free products to the benefit of adults who would otherwise continue to smoke, society, the company, its shareholders and its other stakeholders. PMI is a leading international tobacco company engaged in the manufacture and sale of cigarettes, as well as smoke-free products, associated electronic devices and accessories, and other nicotine-containing products in markets outside the U.S. In addition, PMI ships versions of its IQOS Platform 1 device and consumables to Altria Group, Inc. for sale under license in the U.S., where these products have received marketing authorizations from the U.S. Food and Drug Administration (FDA) under the premarket tobacco product application (PMTA) pathway; the FDA has also authorized the marketing of a version of IQOS and its consumables as a Modified Risk Tobacco Product (MRTP), finding that an exposure modification order for these products is appropriate to promote the public health. PMI is building a future on a new category of smoke-free products that, while not risk-free, are a much better choice than continuing to smoke. Through multidisciplinary capabilities in product development, state-of-the-art facilities and scientific substantiation, PMI aims to ensure that its smoke-free products meet adult consumer preferences and rigorous regulatory requirements. PMI's smoke-free product portfolio includes heat-not-burn and nicotine-containing vapor products. As of September 30, 2023, PMI's smoke-free products are available for sale in 82 markets in key cities or nationwide, and PMI estimates that approximately 19.7 million adults around the world, excluding Russia and Ukraine have already switched to IQOS and stopped smoking. For more information, please visit www.pmi.com and www.pmiscience.com.
  • 2 Months Ago

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Manager/Senior Manager, Retail Compliance & Regulatory Affairs
  • Retail Industry Leaders Association
  • Washington, DC FULL_TIME
  • RILA is growing! (Apply here - https://app.builtforteams.com/rila/jobs/fd75441a)At Retail Industry Leaders Association (RILA), we convene top retail executives and decision-makers, advocate for the re...
  • 1 Month Ago

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Regulatory Affairs Specialist US
  • Clinglobal Group
  • Washington, DC OTHER
  • Regulatory Affairs Specialist - United States of America Clinglobal is an Animal Health Contract Research Organisation and supports our global operations in various countries. We are currently looking...
  • 1 Month Ago

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VP, Legal - Regulatory Affairs
  • US01 Illumina, Inc.
  • Washington, DC FULL_TIME
  • What if the work you did every day could impact the lives of people you know? Or all of humanity? At Illumina, we are expanding access to genomic technology to realize health equity for billions of pe...
  • 15 Days Ago

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Director, Regulatory Affairs
  • American Pharmacists Assoc
  • Washington, DC FULL_TIME
  • Director, Regulatory AffairsWashington, D.C.The American Pharmacists Association is the largest association representing pharmacists in all practice settings in the United States and is the only organ...
  • 21 Days Ago

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Public Policy and Regulatory Affairs
  • Cohere
  • Washington, DC FULL_TIME
  • Who are we?Our mission is to scale intelligence to serve humanity. We’re training and deploying frontier models for developers and enterprises who are building AI systems to power magical experiences ...
  • 2 Months 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...
  • 5/23/2024 12:00:00 AM

Washington, D.C. is located in the mid-Atlantic region of the U.S. East Coast. Due to the District of Columbia retrocession, the city has a total area of 68.34 square miles (177.0 km2), of which 61.05 square miles (158.1 km2) is land and 7.29 square miles (18.9 km2) (10.67%) is water. The District is bordered by Montgomery County, Maryland to the northwest; Prince George's County, Maryland to the east; Arlington County, Virginia to the south; and Alexandria, Virginia to the west. The south bank of the Potomac River forms the District's border with Virginia and has two major tributaries: the An...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Regulatory Affairs Manager jobs
$154,115 to $217,381

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