Regulatory Affairs Specialist jobs in Anderson, IN

Regulatory Affairs Specialist supports the oversight of regulatory matters and strategy implementation to ensure the organization complies with applicable regulations. Prepares filings and tracks applications for licensing, certification, and permits and interacts with governmental officials during the regulation and certification process. Being a Regulatory Affairs Specialist monitors compliance with existing regulations and upcoming or changing regulations. Performs impact analysis of regulatory changes and produces status reports. Additionally, Regulatory Affairs Specialist participates in processes to report, investigate, and addresses any issues of non-compliance. Typically requires a bachelor's degree. Typically reports to a supervisor or manager. The Regulatory Affairs Specialist occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. To be a Regulatory Affairs Specialist typically requires 2 -4 years of related experience. (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.

  • 9 Days Ago

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Benefits Specialist
  • TF Partners Inc.
  • Muncie, IN FULL_TIME
  • TF Partners Inc is calling all customer service rockstars to apply to join our amazing team as a full-time Benefits Specialist! WHY YOU SHOULD JOIN OUR TEAM We are an agency that offers a supportive w...
  • 1 Month Ago

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Transition specialist
  • Capleo Global LLC
  • Pendleton, IN FULL_TIME
  • Job Title : Transition Specialist / CSR Location : Pendleton, IN 46064 (100% Onsite from Day 1) Duration : 6 Months Contract (with a possible extension) Job Description : Facilitate the implementation...
  • 7 Days Ago

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Marketing specialist
  • Marion Health
  • Marion, IN FULL_TIME
  • Job Summary Strategically implement the marketing plan's paid verticals to support clinical areas, ancillary programs and the hospital system as a whole. Develop and coordinate the identification of m...
  • 7 Days Ago

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Employment Specialist
  • Developmental Services, Inc. - Kokomo
  • Kokomo, IN FULL_TIME
  • Our Vision The elimination of barriers that restrict individuals with disabilities from community inclusion. We strive to eliminate all barriers that keep our clients from being a part of their commun...
  • 7 Days Ago

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To Go Specialist
  • Olive Garden
  • Anderson, IN OTHER
  • For this position, pay will be variable by location - See additional job details and benefits below.Our Winning Family Starts With You! Check out these great benefits!Flexible schedules to help you ba...
  • 7 Days Ago

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0 Regulatory Affairs Specialist jobs found in Anderson, IN area

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Patient Access Specialist
  • Aspire Indiana Health, Inc
  • Anderson, IN
  • WE SERVE ALL. WE HIRE ALL. WE ACCEPT ALL. Now interviewing for a Patient Access Specialist! Aspire Indiana Health is a n...
  • 4/14/2024 12:00:00 AM

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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...
  • 4/13/2024 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...
  • 4/13/2024 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...
  • 4/13/2024 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...
  • 4/13/2024 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...
  • 4/13/2024 12:00:00 AM

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Financial Representative - Carmel, IN
  • Fidelity TalentSource LLC
  • Carmel, IN
  • Job Description: Financial Representative We believe that as a Financial Representative, you make a key impact on the br...
  • 4/12/2024 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...
  • 4/12/2024 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 Affairs Specialist jobs
$70,334 to $94,258
Anderson, Indiana area prices
were up 1.3% from a year ago

Regulatory Affairs Specialist in Long Beach, CA
In addition to keeping informed of licensing and legal documentation requirements, a regulatory affairs specialist is involved in less-visible yet vastly important industry issues, such as packaging and labeling.
December 16, 2019
Regulatory Affairs Specialist in Albuquerque, NM
Coordinate and document internal regulatory processes, such as internal audits, inspections, license renewals, or registrations.
February 20, 2020
Regulatory Affairs Specialist in Petaluma, CA
Becoming a regulatory affairs specialist is one of the most common ways to break into the industry.
February 10, 2020
The regulatory affairs industry plays an important role in ensuring the safety of countless products that Americans use every day—from food and beverages to pharmaceuticals and medical devices to electronics and more.
February 02, 2020