Regulatory Affairs Specialist Jobs in New Jersey
24 New Jersey Regulatory Affairs Specialist jobs found on Monster.Jobs 1 to 20 of 24
Senior Regulatory Affairs Specialist Participate on product development teams and implement strategies to ensure US, EU, Japan and other international regulatory requirements are incorporated as part of the development process • Author and maintain US FDA and EU submissions and other regulatory documents to obtain approval to bring new or modified products to market • Lead post market submissions...
Primary Purpose of this position: With modest supervision, this Regulatory Specialist II position provides regulatory support to the successful commercialization of all personal care product categories, with emphasis on cosmetics and OTC drugs in North America. Essential Functions: ? Provide day-to-day regulatory support for new product development and commercialization projects. ? Review and appr...
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...
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...
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...
TechData is hiring SAS Programmer (Some positions can be telecommute), Biostatistician,QA/Consultant, Senior Assoc. Dir. Medical Affairs, Clinical Data Manager, Medical Writer, Technical Writing Specialist, Clinical Study Manager, Oracle Clinical Global Librarian - Oncologyfor our pharmaceutical clients in Northern NJ. Please see below requirements and send your resume to: dan.chen@techdataservice...
IS Specialist/IS Consultant - DOMASYS - RD19399 Description JOB SUMMARY:The Solution Leader (SL) for DOMASYS is a member of the RD 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-sour...
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...
Johnson & Johnson companies are equal opportunity employers. Senior Therapeutic Specialist, Medical Information Center (1 of 2)-2007131209 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 mos...
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...
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...
A New Beginning-Genesis 2 Multiple
Principal Specialist CQA Auditor Pharmaceutical / Biotech exp in Research & Development New Jersey Benefits - Full Relocation Assistance Available - Yes Bonus Eligible - Yes Interview Travel Reimbursed - Yes 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 responsib...
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...
TechData is hiring for SAS/Statistical Programmer(Some positions can be telecommuting), Biostatistician(Some can be telecommuting), Sr. Clinical Data Manager, Clinical Study Manager, Publisher, Medical Data Specialist, Contract Administratorfor our pharmaceutical clients in Northern NJ. We also have similar positions in MA, PA, MD, DE, NC and CA. Please see below requirements and send your resume...
TechData is looking forBiostatistician, Statistical Programmer (Some positions can be telecommuting), Sr. SAS programmer analyst (Data management group), Submission Publisher, Senior Medical Data Specialist/Medical Dictionary Coding, Contract Recruiter (Contract to Hire),Sr. Clinical Data Manager, Sr. Clinical Study Manager Medical Writer(remote)for our pharmaceutical clients in multiple locations...
Pharmalink Consulting - Global Regulatory Affairs Consultants
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Regulatory Affairs Associate
$38,760.00 - $94,500.00
Typical Salary for Regulatory Affairs Associate in New Jersey
Source: Monster.com Careerbenchmarking Tool
Education / Training
Some College Coursework Completed
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.
Maintains records by updating databases; recording and filing submissions.
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