Regulatory Affairs Specialist Jobs in Raritan, New Jersey
14 Raritan, NJ Regulatory Affairs Specialist jobs found on Monster.Jobs 1 to 14 of 14
The Regulatory Operations Specialist is responsible for preparing and publishing documentation is support of international and U.S. FDA submissions, expert user of regulatory information systems, including the regulatory release process and regulatory data/documentation system. Position Responsibilities Maintain current knowledge to ensure compliance to the applicable regulatory and corporate st...
Firmenich is a leading International company with headquarters in Geneva, Switzerland. Our reputation for excellence as a creator and manufacturer of specialty chemicals, flavors and perfumery products is recognized worldwide. From our award-winning fragrances to our irresistible candy ingredients, our team has been combining experience and innovation to perfume and flavor our clients' products fo...
COMPANY PROFILE: For more than 80 years, the name Terumo® has been synonymous with innovative medical devices. From its start as a manufacturer of clinical thermometers, Terumo has grown worldwide to a position of leadership in such areas as hollow fiber technology, blood management systems, and the creation of new technologies in endovascular therapy. Terumo has distinguished itself as a high qua...
Description: Reporting to the Manager of Regulatory Affairs. Under supervision, this role provides strategic and operational CMC regulatory direction and documentation for projects/products covering development, registration and approval/post approval activities. Key Responsibilities: · Under supervision, provide and/or implement CMC regulatory strategies for development projects or marketed produ...
Johnson & Johnson companies are equal opportunity employers. Regulatory Affairs Leadership Development Program - United States-00000G1K Description The Medical Devices and Diagnostics (MD&D) franchise of Johnson& Johnson is recruiting a Regulatory Affairs Specialist II to join the Regulatory Affairs Leadership Development Program (RALDP). This is a permanent, full-time position with J&J. Positions...
Our client, a global pharmaceutical organization is seeking a Regulatory Affairs Specialist-Publishing to join their expanding team. This is an exciting time to join this organization as they recently brought several new products to market. Position offers tremendous growth, competitive compensation, comprehensive benefits and a rewarding working environment. Position Requirements: · BS degree in...
Are you a Regulatory Affairs specialist with global experience? If so, review the job description below and submit your resume for this full-time, permanent opportunity with a highly reputable pharmaceutical company. The Global Regulatory Affairs Manager is responsible for providing technical regulatory leadership to ensure compliance of commercial products and for the development of Chemistry, Ma...
A highly distinguished & highly reputable pharmaceutical corporation is currently seeking a qualified and experienced Drug Safety Data Specialist to work in Plainsboro, NJ. Job Role: • Responsible for collection and processing of spontaneous and clinical trial adverse event and pregnancy reports, which includes data entry and verification of information into the safety database. • Responsible for...
Requisition ID 18539BR Title Safety Data Specialist- Case Management II Job Category Regulatory Affairs Job Description PURPOSE: Responsible for the daily processing of post-marketing and clinical trial adverse events. To ensure compliance with FDA regulations regarding collection, verification, and maintenance of records concerning adverse drug/device reports. Responsible for telephone and writte...
Johnson & Johnson companies are equal opportunity employers. Senior Therapeutic Specialist- Medical Information Center (MIC)-9720131017 Description Janssen Scientific Affairs, L.L.C., is recruiting for a Senior Therapeutic Specialist, Medical Information Center (MIC) located in Titusville, NJ. Janssen Pharmaceuticals Companies of Johnson & Johnson are dedicated to addressing and solving the most i...
JOB SUMMARY: The Solution Leader (SL) for DOMASYS is a member of the R&D IS team, reporting to the Head of Resource Center, and is responsible for providing global leadership to develop the roadmap of business and application requirements, coordinating the activities of a team, and leveraging services, external relationships and/or out-sourcing management to ensure solution lifecycle management, t...
This position requires someone who is fluent in French. Native speaker preferred. Read, write, and communicate fluently. Knowledge of Medical Terminology in French is required. High volume call center environment. Provides product information support within the Drug Information Center, Medical Information Dept. for COMPANY products. Individual will be responsible for providing information to both...
Job Summary: The Principal Specialist is responsible for the initiation, conduct, and follow-up of audits as assigned by CQA Management. Within the frame of the Principal Specialist's mission and responsibilities, the audits and activities require proven ability to independantly interact with all internal and external (e.g. Vendors / CRO) operational staff (e.g. Project Teams, Clinical Operations,...
Johnson & Johnson companies are equal opportunity employers. PRINCIPAL ENGINEER- Metallurgy-0044130530 Description The Ethicon Surgical Care business offers a broad range of products, platforms and technologies-including sutures, surgical staplers, clip appliers, trocars and synthetic mesh devices-that are used in a wide variety of minimally invasive and open surgical procedures. Specialties inclu...
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Maybe it is just me, but doesn't the dr, usually have you sign hippa at?
Your very first appointment, before anything else is done, I feel for hippa to be more respectable and help ful to the individual it should be signed on a case by case basis to more carefully evaluate...
Whats the future scope of drug regulatory affaire..?
i am doing this can u tell me whats the job prospects and scope in futuer
I dont know if I want to go to medical school or be a doctor anymore. advise?
So the more i hear about how hard everything will be in med school and how it doesnt stop there but the work of a doctor is very demanding and that they have no lives it all just seems so depressing t...
Please let me know soon???
Hello, I am currently looking for jobs related to biological research and pharmaceutical research. has anyone heard of EspoirBridge Recruiters? I submitted some of my information to them, but I jus...
Dropping out of medical school, advice on a career transition?
Finished my first year of medical school and have decided that medicine and the massive amount of debt is not for me. I'd like to pursue a career in financial services if anyone has suggestions on how...
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Regulatory Affairs Associate
$42,000.00 - $84,700.00
Typical Salary for Regulatory Affairs Associate in Raritan
Source: Monster.com Careerbenchmarking Tool
Education / Training
Source: Monster.com Careerbenchmarking Tool
Regulatory Affairs Associate
Ensures regulatory compliance by determining submissions requirements; assembling and preparing submissions; collecting and providing information.
Rate of Growth
Size of Industry in 2006:
Source: Bureau of Labor Statistics, May 2006
Prepares regulatory submissions by assembling, reviewing, and coordinating required information; compiling and preparing responses to regulatory agency questions.
Prepares reports by providing information to support product claims and advertising; collecting, analyzing, and summarizing regulatory data and trends.
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