Regulatory Relations Specialist jobs in Anderson, IN

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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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 help patients around the globe. Our proven heritage combined with a pioneering approach are the hallmarks to deliver innovation, excellence and unparalleled service.


    With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life-threatening diseases to over 14 million patients annually. The name ‘Curium’ honors the legacy of pioneering radioactive researchers Marie and Pierre Curie, after whom the radioactive element curium was named and emphasizes our focus on nuclear medicine. The tagline ‘Life Forward’ represents our commitment to securing a brighter future for all those we serve: An enhanced quality of care for our patients. A trusted partner to our customers. A supportive employer to our valued team.


    Summary of Position

    The Regulatory Affairs Technical Writer supports projects related to Curium’s business strategy in the space of sterile drug manufacturing including reactor and cyclotron derived new products. This position focuses on the creation, revision, and maintenance of technical documentation necessary for regulatory submissions and compliance within a regulated industry, such as pharmaceuticals, biotechnology, or medical devices. A keen attention to detail, strong writing skills, and the ability to synthesize complex information into clear, concise, and compliant documentation are essential.


    Essential Functions

    • Draft, revise, and finalize technical documents required for regulatory submissions, ensuring compliance with local and international regulatory standards and guidelines.
    • Utilize technical writing strategies to ensure content of documentation is clear, concise, and complete.
    • Work closely with subject matter experts (SMEs) across various departments to gather, interpret, and accurately represent data and information in regulatory documents.
    • Participate in process and equipment testing to learn systems being documented.
    • Review and edit technical documents for clarity, grammar, format, and compliance. Ensure all documentation is accurate, up-to-date, and adheres to established standards and SOPs.
    • Manage the lifecycle of regulatory documents, including version control, archiving, and retrieval. Ensure the integrity and confidentiality of sensitive information.
    • All programs must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.).

    Requirements

    • Bachelor Degree or equivalent work experience required.
    • 3 or more years of relevant experience in technical writing required.
    • Experience with technical writing in a regulatory affairs environment preferred.
    • Experience in the pharmaceutical, biotechnology, or medical device industry is highly preferred.
    • Must be able to communicate clearly in English and have solid communication skills including grammar and composition.
    • Demonstrated understanding of GMP / cGMP regulations.
    • Skill in communication, written and verbal with the ability to interact with cross-functional teams.
    • Proven time management skills and a strong attention to detail.
    • Proven ability to manage and coordinate multiple projects in a fast-paced, highly professional environment.
    • Ability to work well with others and independently.
    • Able to read, understand and follow work instructions in a safe, accurate and timely manner.
    • Proficiency in document management systems and Microsoft Office Suite. Familiarity with eCTD structure and requirements is desirable.

    Working Conditions

    • Willingness to work in plant producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels.
    • Responsibilities include the ability to lift up to 70 pounds, kneeling, crouching, twisting the upper body, walking, bending, stooping, pushing, pulling, reaching, must be able to physically negotiate stairs and evacuation ladders with or without accommodation, wear and operate safety equipment, enter vessels, and inspect equipment.
    • Material handling devices (e.g., hand truck, fork truck, and conveyors) are used when possible, however, use of proper lifting and movement techniques is necessary to prevent injury.
    • Must be willing to wear a variety of Personal Protective Equipment (PPE) and hearing protection as needed.
    • May be required to sit or stand for long periods of 8 hours a day while performing duties.
    • Must possess good hand-eye coordination; close attention to detail is required.
    • Must be able to work indoors and outdoors with exposure to mechanical/moving parts, hazards including corrosive, flammable and toxic material, dust, dirt, odors, and irritants.
    • Willingness to complete safety training within allotted timeframes, and work in a team-based environment.
    • Must be able to work outside of regular work hours, including off shift, weekend, and holiday work as business needs require.

    Disclaimer

    The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.


    Equal Opportunity Employer

    Curium is an equal opportunity employer and believes everyone deserves respect, dignity and equality. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

  • 17 Days Ago

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Regulatory Affairs Manager-Clinical
  • Synergy Solutions
  • Noblesville, IN CONTRACTOR
  • Initial 9 month onsite contract with possible extension and/or conversion to permanent employment. The main focus of this position will be on new submissions associated with new chemical entity (NCE) ...
  • 6 Days Ago

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(Contractor) Senior Manager Regulatory Affairs - CMC
  • Curium Pharma
  • Noblesville, IN CONTRACTOR
  • (Contractor) Senior Manager Regulatory Affairs - CMC Date: Apr 4, 2024 Location: Noblesville, IN, United States About Curium Curium is the world's largest nuclear medicine company with more than a cen...
  • Just Posted

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Community Relations Director
  • Northwood Manor
  • Marion, IN FULL_TIME
  • Location Information Northwood Manor is a beautiful community in Marion, IN, with more than 50 units offering independent living. Key Responsibilities At this time, we are seeking a Community Relation...
  • 20 Days Ago

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Director of Public Relations
  • Kokomo Healthcare Center
  • Kokomo, IN FULL_TIME
  • Kokomo Healthcare Center, a member of the CommuniCare Health Services, is seeking an experienced health care professional with sales and marketing abilities for the position of Director of Public Rela...
  • 1 Month Ago

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Customer Relations Associate
  • Bass Pro, LLC
  • Noblesville, IN FULL_TIME
  • POSITION SUMMARY:The Customer Relations Associate performs various Customer Service activities, to include greeting and acknowledging all customers in a prompt and friendly manner, handling merchandis...
  • 23 Days Ago

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0 Regulatory Relations Specialist jobs found in Anderson, IN area

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Personal Lines Account Manager
  • McGowan Insurance Group
  • Anderson, IN
  • About Us McGowan Insurance Group has a concentrated geographic footprint in the Indianapolis, IN area with a diverse off...
  • 4/23/2024 12:00:00 AM

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Superintendent, Light and Power
  • City Of Anderson
  • Anderson, IN
  • About the Job: Job Category: Light and Power Work Location: 550 Dale Keith Jones Rd, Anderson, IN 46011 Job Type & Durat...
  • 4/23/2024 12:00:00 AM

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Personal Lines Account Manager
  • Mcgowan Insurance Group
  • Anderson, IN
  • About UsMcGowan Insurance Group has a concentrated geographic footprint in the Indianapolis, IN area with a diverse offe...
  • 4/23/2024 12:00:00 AM

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Licensed Therapist
  • Eventus WholeHealth
  • Anderson, IN
  • Job Description Job Description Position Summary: Eventus WholeHealth delivers an integrated model of care to adults who...
  • 4/23/2024 12:00:00 AM

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Experienced Real Estate Agent
  • Carpenter Realtors
  • Anderson, IN
  • Job Description An Experienced Real Estate Agent is a professional with a proven track record in real estate sales. Frie...
  • 4/23/2024 12:00:00 AM

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Real Estate Buyer's Agent
  • Carpenter Realtors
  • Anderson, IN
  • Job Description A Real Estate Buyer's Agent is a real estate agent who helps clients with their home purchasing needs. Y...
  • 4/23/2024 12:00:00 AM

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Entry-Level Real Estate Agent
  • Carpenter Realtors
  • Anderson, IN
  • Job Description A Real Estate Agent plays an essential role in a real estate transaction. Real estate is an exciting ind...
  • 4/23/2024 12:00:00 AM

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Regulatory Affairs Specialist - EPA
  • Elanco Animal Health Incorporated
  • Indianapolis, IN
  • At Elanco (NYSE: ELAN) - it all starts with animals! As a global leader in animal health, we are dedicated to innovation...
  • 4/22/2024 12:00:00 AM

Anderson is a city in and the county seat of Madison County, Indiana, United States. It is the principal city of the Anderson, Indiana Metropolitan Statistical Area which encompasses Madison County. Anderson is the headquarters of the Church of God (Anderson) and home of Anderson University, which is affiliated with Christian denomination. Highlights of the city include the historic Paramount Theatre and the Gruenewald Historic House. The population was 56,129 at the 2010 census. This is down from 70,000 in 1970. Anderson is located at 40°06′00″N 85°40′53″W / 40.100041°N 85.681525°W / 40.10...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Regulatory Relations Specialist jobs
$68,737 to $94,364
Anderson, Indiana area prices
were up 1.3% 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
We are looking for a Marketing Specialist to plan, coordinate and manage marketing campaigns and activities across marketing channels.
February 06, 2020