Regulatory Affairs Specialist Jobs in New Jersey

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23 New Jersey Regulatory Affairs Specialist jobs found on Monster.

Jobs 1 to 20 of 23
Spartan Search Group is the premier placement firm for technical positions both permanent and contract. With a primary focus on the Northeastern USA, we work with all Medical Device companies large and small and are in constant contact with the top tier, game-changing technical leaders in our industry. We are currently working with a major New Jersey-based Medical Device company that has an immedi...
Responsibilities: Excellent employment opportunity for a Regulatory Affairs Specialist in Raritan, NJ area. Manage and oversee the coordination, compilation and submission of regulatory applications to worldwide regulatory agencies, including new licenses/registrations, and will support day to day Regulatory Operations. The ideal candidate will interpret regulatory requirements and develop strateg...
REG AFFAIRS SPECIALIST: RARITAN, NJ 6-24 months The Regulatory Affairs Specialist will be responsible for managing and overseeing the coordination, compilation and submission of regulatory applications to worldwide regulatory agencies, including new licenses/registrations, and will support day to day Regulatory Operations. The ideal candidate will interpret regulatory requirements and develop stra...
Title: Regulatory Affairs Specialist Location: Mahwah NJ, 07430 Positions: 3 (PLEASE REFER!) Requirements: § BA/BS. Engineering strongly preferred § RAC certification desired § Minimum 1+ years’ experience in FDA regulated industry § Working knowledge of Medical Device Regulations (FDA required) Core Responsibilities: § Plan, organize and implement strategies and activities required to procure reg...
Rising pharmaceutical company is seeking a Senior Regulatory Affairs Specialist or Manager level to join their team. The company has a robust clinical pipeline including an upcoming phase III study. This will be an individual contributor role instrumental in all aspects of Regulatory Affairs. This is a tremendous opportunity to work with a collaborative group of scientists and professionals commit...
Johnson & Johnson companies are equal opportunity employers. Regulatory Affairs Leadership Development Program - United States-00000MCJ 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...
Plan, organize and implement strategies and activities required to procure regulatory approval for new and revised product lines. Participate in cross functional team activities from initial stages to securing government approvals and product launch. Ensure compliance to all internal, US, EU and other international requirements and corporate policies and procedures for market approval of medical d...
Regulatory Specialist needed for a contract opportunity with Yoh's client located in Berkeley Heights, NJ. The Big Picture - Top Skills You Should Possess: - Regulatory Intelligence and Policy What You'll Be Doing: - Develop effective and systematic approaches to regulatory intelligence information and report activities, including the monitoring of industry sources of information, intelligence and...
Regulatory Specialist will provide regulatory and quality support to following business segments: (Human Nutrition, Animal Nutrition, Pharma and Flavors and Fragrances) for Fortune 500 company in the chemical industry. Regulatory Specialist (Chemist) Job Responsibilities · Manages and organizes all group and individual Site Audits. · Requires coordination with various site representatives and cust...
A Regulatory Documentation Specialist needed for a contract opportunity with Yoh's client located in Edison, NJ The Big Picture - Top Skills You Should Possess: - Regulatory submissions - Publishing tools (ISI Toolbox, Documentum) - Clinical Documentation What You'll Be Doing: - Perform the preparation of regulatory submissions in paper format. The ability to prepare submissions in electronic form...
Regulatory Specialist will provide regulatory and quality support to following business segments: (Human Nutrition, Animal Nutrition, Pharma and Flavors and Fragrances) for Fortune 500 company in the chemical industry. Regulatory Specialist (Chemist) Job Responsibilities Manages and organizes all group and individual Site Audits. Requires coordination with various site representatives and customer...
The Regulatory Affairs Sr. is responsible for 1) supervising, coordinating, compiling, and submitting applications to FDA, the EU and other regulatory bodies, 2) working with development teams and management to ensure rapid and timely approval of new devices and continued regulatory support of marketed devices including review of labeling and promotional materials, 3) interacting with regulatory a...
Job Description: Regulatory Affairs Specialist BA/BS in Scientific discipline required. Engineering strongly preferred RAC certification desired Plan, organize and implement strategies and activities required to procure regulatory approval for new and revised product lines. Participate in cross functional team activities from initial stages to securing govenrment approvals and product launch. Ensu...
TechData is hiring SAS Programmer (Some positions can be telecommute), Biostatistician(Some can be telecommute), Clinical Research Scientist/Clinical manager, Contract Specialists, Outsourcing Manager, Informed Consent Setup and study start up, Sr. Clinical Data Managerfor our pharmaceutical clients in Northern NJ. Please see below requirements and send your resume to: *****...
TechData is hiring SAS Programmer (Some positions can be telecommute), Biostatistician(Some can be telecommute), Clinical Research Scientist/Clinical manager, Contract Specialists, Outsourcing Manager, Informed Consent Setup and study start up, Sr. Clinical Data Managerfor our pharmaceutical clients in Northern NJ. Please see below requirements and send your resume to: *****...
TechData is looking for Talent Identification Specialist, Outcome Research Biostatistician, Marketing Consultant, Biostatistician (one can be telecommute), SAS Programmer (some can be remote), Clinical Trial Manager, (One is a director level)for our pharmaceutical clients in Central NJ. Please see below requirements and send your resume to: *****. TechData is a leading pro...
Job Description : Permanent position for a Quality Systems Specialist providing support to the Quality Systems department by monitoring and maintaining change control and master data systems. Maintaining divisional responsibility for administration of systems including PLM, ERP and MDM. Provides support to change control process including but not limited to ensuring compliance to internal procedur...
TechData is hiring for Oracle Clinical Programmer (Inform, SAS, Jreview), SAS/Statistical Programmer(Some positions can be telecommuting), Biostatistician(Some telecommuting), Drug Safety Specialist, Clinical Data Manager/Data Specialist for our pharmaceutical clients in Central NJ.Please see below requirements and send your resume to: *****. TechData is a leading provider f...
Johnson & Johnson companies are equal opportunity employers. Sr. Therapeutic Specialist, Medical Information Center-2007140325 Description Janssen Scientific Affairs, LLC, 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 important unm...
Contracts Specialist 6 month, renewable contract W2 candidates only Requirement: 2-3 years experience in pharmaceutical services with 4-6 years contract management and/or medical start-up activities including vendor and site contract negotiations and management. Duties Independently negotiates and finalizes confidentiality/non-disclosure agreements, consultancy agreements, clinical trial agreement...
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Answers for Regulatory Affairs Specialist Jobs

Questions & Answers Powered by Yahoo! Answers
Whats the future scope of drug regulatory affaire..?
i am doing this can u tell me whats the job prospects and scope in futuer
Anyone knows whats the basic functions of a International regulatory specialist?
I have been offered a position at a medical devices company as an International Regulatory Specialist. They don't necessarily ask for experience, so I was wondering if anyone can give me some insight...

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Regulatory Affairs Associate

Salaries

$38,760.00 - $94,500.00
Typical Salary for Regulatory Affairs Associate in New Jersey
(110 Respondents)
Source: Monster.com Careerbenchmarking Tool

Education / Training

Bachelor's
38.8%
Master's
38.8%
Associates
9%
Some College Coursework Completed
4.5%
High School
3%
Doctorate
3%
(67 Respondents)
Source: Monster.com Careerbenchmarking Tool

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