Regulatory Affairs Manager jobs in Racine, WI

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 Operations
  • Round Lake, Illinois
  • Round Lake, IL FULL_TIME
  • This is where you save and sustain lives

    At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. 

    Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

    Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. 

    Join us at the intersection of saving and sustaining lives— where your purpose accelerates our mission. 

    What you will be doing:

    • Managing the preparation of regulatory submissions for IND, ANDA, NDA, 510K, AdProm, and other electronic submission types
      • Creating timelines for regulatory filings
      • Providing and maintain templates for authoring.
      • Overseeing authoring and reviewing of regulatory documents
      • QC submission documents
    • Managing external publishing teams supporting submissions in different markets (OUS).
    • Managing Authoring support team working on electronic submissions.
    • Contribute to the development of process improvements and procedural documents.
    • Identifying and assessing regulatory risks and risks to timelines.
    • Providing regulatory updates to the project team on different milestones.
    • Working cross functionally with project management, operations, IT and other functions.
    • Coordinate submission scheduling with regulatory publishing and ensures delivery of high-quality documents.
    • Working closely with other members of the Regulatory team and provide support to their projects as needed.
    • Maintaining archival of submissions and health authority communications in Veeva RIM system.
    • Provide regulatory representation on key meetings, including meetings with health agency.  

    What do you bring:

    • Solid understanding and experience and interpretation of regulatory requirements, with particular emphasis on the US region.
    • Strong organization skills and the ability to track multiple timelines in parallel and manage deadlines.
    • Excellent written and verbal communication and ability to collaborate across functions.
    • Experience with Veeva Vault systems is preferred
    • Strong team player, self-motivated and able to function independently as well as part of a team
    • Able to work on multiple projects concurrently and adapt to a continuously changing environment.
    • BA/BS in a scientific field and 5-7 years of proven experience

    Baxter is committed to supporting the need for flexibility in the workplace. We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite. This policy provides the benefits of connecting and collaborating in person to support our Mission.

    We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $104,000 to $143,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

    The successful candidate for this job may be required to verify that he or she has been vaccinated against COVID-19, subject to reasonable accommodations for individuals with medical conditions or religious beliefs that prevent vaccination, and in accordance with applicable law.

    Equal Employment Opportunity

    Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
                                                                                                                                                                   
    EEO is the Law 
    EEO is the law - Poster Supplement 
    Pay Transparency Policy

    Reasonable Accommodations

    Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

    Recruitment Fraud Notice

    Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

    129996
  • 20 Days Ago

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Regulatory Affairs Specialist
  • Actalent
  • Round Lake, IL OTHER
  • Description: Managing the preparation of regulatory submissions for IND ANDA NDA 510K AdProm and other electronic submission types o Creating timelines for regulatory filings o Providing and maintain ...
  • Just Posted

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Regulatory Affairs Specialist I
  • Primary Talent Partners
  • Round Lake, IL FULL_TIME
  • Primary Talent Partners has an exciting opportunity with our client in Round Lake, Illinois. This is a contract position with a duration of 12 months. C2C candidates will not be considered for this ro...
  • 1 Day Ago

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Regulatory Affairs Associate
  • Infobahn Softworld Inc
  • North Chicago, IL PART_TIME,CONTRACTOR
  • Position will be 100% onsite 5 years experience, preferably in IVD Reg Affairs. Top 5 skills/requirements Reg Affairs, IVD or Medical Device, Project Management, previous Client would be ideal Brief s...
  • 7 Days Ago

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Regulatory Affairs Specialist
  • DivIHN Integration, Inc
  • Bluff, IL FULL_TIME
  • Title: Regulatory Affairs Specialist Location: Abbott Park, ILDuration: 7 Months Description Main Responsibilities Provide regulatory input to product lifecycle planning. Assist in SOP development and...
  • 7 Days Ago

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Regulatory Affairs Associate
  • Collabera
  • North Chicago, IL FULL_TIME
  • Company DescriptionAbout Collabera:Established in 1991, Collabera is one of the fastest growing end-to-end information technology services and solutions companies globally. As a half a billion dollar ...
  • 1 Month Ago

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0 Regulatory Affairs Manager jobs found in Racine, WI area

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Regulatory Affairs Associate
  • GForce Life Sciences
  • North Chicago, IL
  • Regulatory Affairs Associate – On-site near North Chicago, IL (60064) Term & Start • 8-month contract with possibility t...
  • 4/18/2024 12:00:00 AM

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Regulatory Affairs Associate
  • Intellectt Inc
  • North Chicago, IL
  • Role Regulatory Affairs Associate Location North Chicago, Illinois, 60064 Duration 8 Months on W2 Accountability / Scope...
  • 4/18/2024 12:00:00 AM

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Regulatory Affairs Associate - Onsite
  • Viva Usa Inc.
  • North Chicago, IL
  • Title: Regulatory Affairs Associate - Onsite Description: Accountability / Scope: As the professional in the Regulatory ...
  • 4/18/2024 12:00:00 AM

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Regulatory Affairs Associate
  • Gforce Life Sciences
  • Lake Forest, IL
  • Regulatory Affairs Associate Abbott Park, IL Must be able to work on a W2 Job Summary: As an individual contributor, the...
  • 4/18/2024 12:00:00 AM

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Regulatory Affairs Associate
  • Planet Pharma
  • North Chicago, IL
  • Accountability / Scope: As the professional in the Regulatory Affairs function, the individual will assist teams in the ...
  • 4/17/2024 12:00:00 AM

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Regulatory Affairs Associate I
  • Integrated Resources, Inc ( IRI )
  • Round Lake, IL
  • Job Title: Regulatory Affairs Associate I Duration: 12 Months Location: Round Lake, IL 60073 – Hybrid Hybrid - 3 days on...
  • 4/17/2024 12:00:00 AM

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Supply Management Analyst
  • STS Technical Services
  • Wauwatosa, WI
  • STS Technical Services is hiring a Supply Management Analyst in Wauwatosa, Wisconsin. Position Summary: Product Developm...
  • 4/16/2024 12:00:00 AM

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Specialist Regulatory Affairs
  • DivIHN Integration Inc
  • North Chicago, IL
  • DivIHN (pronounced “divine”) is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, C...
  • 4/16/2024 12:00:00 AM

Racine (/rəˈsiːn/ rə-SEEN) is a city in and the county seat of Racine County, Wisconsin, United States. It is located on the shore of Lake Michigan at the mouth of the Root River. Racine is located 22 miles south of Milwaukee. As of the 2010 U.S. census, the city had a population of 78,860, making it the fifth-largest city in Wisconsin. Its median home price of $103,625 makes it one of the most affordable cities in Wisconsin to buy a home. In January 2017, it was rated "the most affordable place to live in the world" by the Demographia International Housing Affordability survey. Racine is th...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Regulatory Affairs Manager jobs
$134,178 to $189,265
Racine, Wisconsin area prices
were up 1.8% from a year ago

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The ideal candidate will have strong working knowledge of the agrochemical regulatory requirements.
December 24, 2019
Regulatory Affairs Manager in Stockton, CA
The world’s leading research-based pharmaceutical and healthcare companies is looking for a Regular Affairs Manager.
December 01, 2019
Regulatory Affairs Manager in Pierre, SD
Pharmaceutical companies, cosmetics manufacturers, food producers, and medical device suppliers hire regulatory affairs managers to make sure they adhere with all regulations.
February 01, 2020