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
Our client in Mahwah, NJ is seeking Regulatory Affairs Specialist. This is an immediate need. Kindly respond to this positing if you are interested. 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...
Regulatory Affairs Senior Specialist (Great Temp to Perm opportunity) Basking Ridge, NJ Our biopharmaceutical client is currently expanding their Regulatory Affairs team, and is seeking an experienced Regulatory Affairs Senior Specialist. This position offers very strong compensation, career growth and a great work environment! This is the perfect opportunity for an experienced Regulatory Affairs...
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...
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...
A highly regarded Pharmaceutical Organization is currently recruiting for a CMC Consultant for a critical assignment ongoing until the end of 2014. Based in Princeton NJ, this company specializes in cutting edge Oncology therapeutics. This is an ideal opportunity for an experienced CMC Consultant looking for a new contract to make a critical impact at a Pharmaceutical company. The purpose of this...
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 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...
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...
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Answers for Regulatory Affairs Specialist Jobs

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Regulatory affairs specialist career?
From what i've been reading, this seems like a lucrative career..can anyone else give me some more information about the field? I know the requirements are a bachelors, so would it help if i worked to...
What can I do with a BS degree in Political Science? My 'specialization' is in Foreign Affairs.?
I know I can teach, but is there any other paths I could choose too. I also am aware that I could attend Law School.

Legal Career Tools

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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