Regulatory Relations Specialist jobs in Easton, PA

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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Sr. Regulatory Affairs Specialist
  • B. Braun Medical Inc.
  • Center, PA FULL_TIME
  • Overview

    About B. Braun 

     

    B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the B. Braun Group of Companies in the U.S., which includes B. Braun Interventional Systems, Aesculap® and CAPS®.

     

    Globally, the B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise® philosophy, B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about B. Braun Medical, visit www.BBraunUSA.com.

    Responsibilities

    Position Summary:

     

     

    Responsibilities: Essential Duties

    • Plans and prepares registration documents for marketing approval of drug and device products in the US and in foreign countries.  
    • Serves as a regulatory liaison for new product development and make regulatory assessments of proposed changes to existing products for impact to regulatory documentation.  
    • Provides strategic input and guidance to project teams in conjunction with supervisor.
    • Plans and prepares dossiers for registration of drug and device products.
    • Independently reviews and analyzes proposed modifications to drug and device products for regulatory impact.
    • Independently reads, reviews, interprets and keeps current with regulations and publications regarding drug and device products and communicate within the department.
    • May oversee and direct the work of other Regulatory Affairs professionals.
     The job function listed is not exhaustive and shall also include any responsibilities as assigned by the Supervisor from time to time. 

    Expertise: Knowledge & Skills

    • Requires full working knowledge of relevant business practices and procedures in professional field. Uses standard theories, principles and concepts and integrates them to propose a course of action.
    • Work under minimal supervision. Relies on experience and judgement to plan and accomplish assigned goals. May periodically assist in orienting, training, assigning and checking the work of lower level employees. Referring only complex problems and issues
    • Judgement is required in resolving complex problems based on experience.
    • Contacts are primarily with department supervisors, leads, subordinates, and peers. Frequent contact with external contractors/vendors.

    #ID#LI#MSL

    Target Based Range

    $92,830 - $116,030

    Qualifications

    Expertise: Qualifications -Education/Experience/Training/Etc

     

    Required:

    • Bachelor's degree required.
    • 06-08 years related experience required.
    • Applicable industry/professional certification required.
    • Regular and predictable attendance
    • Frequent business travel required, Secrecy and invention agreement and non-compete agreement, Ability to work non-standard schedule as needed

     

    While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee frequently is required to use hands to handle or feel and reach with hands and arms. The employee is occasionally required to stand and walk. The employee must occasionally lift and/or move up to 20 pounds.

     

     

     

     

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    Additional Information

    Responsibilities: Other Duties:

     

    The preceding functions have been provided as examples of the types of work performed by employees assigned to this position. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed in this description are representative of the knowledge, skill, and/or ability required. Management reserves the right to add, modify, change or rescind the work assignments of different positions due to reasonable accommodation or other reasons.

     

    Physical Demands:

    While performing the duties of this job, the employee is expected to:

    • Light work - Exerting up to 20 lbs of force occasionally, and/or up to 10 pounds of force frequently, and/or a negligible amount of force constantly to move objects.

    Lifting, Carrying, Pushing, Pulling and Reaching:

    • Occasionally:Reaching upward and downward, Push/pull, Stand, Visual Acuity with or without corrective lenses
    • Frequently:Sit
    • Constantly:N/A

    Activities:

    • Occasionally:Climbing stairs/ladders, Handling, Push/pull, Reaching upward and downward, Standing, Walking
    • Frequently:Finger feeling, Hearing - ordinary, fine distinction, loud (hearing protection required), Seeing - depth perception, color vision, field of vision/peripheral, Sitting , Talking - ordinary, loud/quick
    • Constantly:N/A

    Environmental Conditions:

    • Occasionally:Proximity to moving parts, Exposure to toxic or caustic chemicals (in most areas)
    • Frequently:N/A
    • Constantly:N/A

    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.

    • Noise Intensity:Low
    • Occasionally:N/A
    • Frequently:N/A
    • Constantly:Office environment

     

    Referral Amount

    Notices

    Equal Opportunity Employer Veterans/Disabled

  • 1 Month Ago

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Manager of Regulatory Affairs
  • Tyber Medical LLC
  • Bethlehem, PA FULL_TIME
  • DescriptionResponsible for managing the regulatory affairs activities throughout the organization. Manages and compiles regulatory submissions in the USA, EU and other jurisdictions as required. Requi...
  • 21 Days Ago

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Director of Compliance and Regulatory Affairs
  • Sharp Packaging Services
  • Allentown, PA FULL_TIME
  • SUMMARYThe Director of Compliance & Regulatory Affairs leads a cGMP, FDA and DEA compliance program for Sharp’s three US Commercial Packaging locations in Pennsylvania. Reporting to the VP Quality for...
  • 1 Month Ago

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Accounting and Regulatory Reporting Manager
  • The Cigna Group
  • Singapore, PA OTHER,FULL_TIME
  • The job profile for this position is Accounting Supervisor, which is a Band 3 Management Career Track Role.Excited to grow your career?We value our talented employees, and whenever possible strive to ...
  • 1 Month Ago

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Sr. Life Sciences / Regulatory Attorney
  • B. Braun Medical Inc.
  • Bethlehem, PA FULL_TIME
  • Overview About B. Braun B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry...
  • 1 Month Ago

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Client Relations Manager
  • PSA BDP
  • Allentown, PA FULL_TIME
  • PSA BDP, a member of the PSA Group, is a leading provider of globally integrated and port-centric supply chain, transportation, and logistics solutions. The company is headquartered in Philadelphia, P...
  • 1 Day Ago

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0 Regulatory Relations Specialist jobs found in Easton, PA area

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Senior Regulatory Affairs Specialist
  • Bausch + Lomb
  • Bridgewater, NJ
  • Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of ...
  • 4/26/2024 12:00:00 AM

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USA-Regulatory Affairs Specialist II (Clinical)
  • eTeam Inc.
  • Bridgewater, NJ
  • Regulatory Affairs Specialist II (Clinical) Bridgewater, NJ-100% Remote 7 Months contract Pay Rate: $45-55/hr on w2 Cand...
  • 4/24/2024 12:00:00 AM

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CMC Regulatory Affairs Specialist
  • Spectraforce Technologies Inc
  • Bridgewater, NJ
  • Job title: CMC Regulatory Technical Writer II Location: Bridgewater, NJ, Hybrid Duration: 1 year SHIFT SCHEDULE 1st shif...
  • 4/23/2024 12:00:00 AM

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CMC Regulatory Affairs Specialist
  • Spectraforce Technologies Inc
  • Bridgewater, NJ
  • Job title: CMC Regulatory Technical Writer II Location: Bridgewater, NJ, Hybrid Duration: 1 year SHIFT SCHEDULE 1st shif...
  • 4/23/2024 12:00:00 AM

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Regulatory Affairs Specialist Team Lead
  • The Fountain Group LLC
  • Bridgewater, NJ
  • The Fountain Group are a national staffing firm and are currently seeking a Regulatory Affairs Lead for a prominent Phar...
  • 4/23/2024 12:00:00 AM

B
Sr. Regulatory Affairs Specialist
  • B. Braun Medical Inc. (US)
  • Bethlehem, PA
  • Responsibilities: Essential Duties Plans and prepares registration documents for marketing approval of drug and device p...
  • 4/22/2024 12:00:00 AM

B
Sr. Regulatory Affairs Specialist
  • B. Braun
  • Center Valley, PA
  • About B. Braun B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and mark...
  • 4/22/2024 12:00:00 AM

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Lead Regulatory Affairs Specialist
  • Globus Medical, Inc.
  • Audubon, PA
  • About Us: At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of ...
  • 4/22/2024 12:00:00 AM

Easton is a city in and the county seat of Northampton County, Pennsylvania, United States. The city's population was 26,800 as of the 2010 census. Easton is located at the confluence of the Delaware River and the Lehigh River, roughly 55 miles (89 km) north of Philadelphia and 70 miles (110 km) west of New York City. Easton is the easternmost city in the Lehigh Valley, a region of 731 square miles (1,893 km2) that is home to more than 800,000 people. Together with Allentown and Bethlehem, the Valley embraces the Allentown-Bethlehem-Easton metropolitan area, including Lehigh, Northampton, an...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Regulatory Relations Specialist jobs
$74,676 to $102,516
Easton, Pennsylvania area prices
were up 1.5% 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
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