Regulatory Affairs Specialist Jobs in New Jersey

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21 New Jersey Regulatory Affairs Specialist jobs found on Monster.

Jobs 1 to 20 of 21
Regulatory Affairs Specialist We have an immediate contract opportunity with a large F500 client in the Franklin Lakes, NJ area. You will manage activities and procedures associated with complaints concerning BD MS, DC, PAS products. You would also be accountable for setting own work direction and completing work tasks. Supervise the processing of customer complaints, Medical Device Reports (MDR),...
Position : Regulatory Affairs Specialist [#7991] Location : 1 Becton Drive Franklin Lakes NJ 07417 UNITED STATES Duration : 5 +Months Contract[Possible extension] Rate : $41.55/hr on W2 (All inclusive) Start Time : 8:00 AM End Time : 5:00 PM Total Hours/week : 40.00 Client : Medical Qualifications: 1. 1-2 years Regulatory Affairs experience in medical device/in vitro diagnostic device companies. 2...
Job Description : Permanent position for a Regulatory Affairs Specialist to maintain compliance for Class II and Class III medical devices. Responsible for compliance documentation with 510(k), FDA and CE Mark submissions. Utilize Trackwise for regulatory filings. Job Requirements : Bachelors Degree in a related field. Minimum 5 years experience with Regulatory Affairs and Compliance for the medic...
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...
Job Description Posting date: May 15, 2014 Position Summary: This position is responsible for managing the CMC (Chemical Product Manufacturing and Controls) compliance of Thermo Fisher Scientific – Global Chemicals products that include hazardous goods, laboratory and analytical reagents, Multi Compendia products, Production chemicals, Class 1 devices, and stains and indicators. Chemical classific...
Posting date: July 10, 2014 Position Summary: Lead and perform regulatory and compliance activities for the company’s regulated products (Multi compendia Production chemicals, cGMP products and medical device products) as directed with primary responsibility for USFDA and Secondary responsibilities for MHRA, TGA, SFDA. Provide International (outside North America) regulatory submission support. Co...
Job Description Posting date: May 6, 2014 Position Summary: Lead and perform regulatory and compliance activities for the company’s regulated products (Multi compendia Production chemicals, cGMP products and medical device products) as directed with primary responsibility for USFDA and Secondary responsibilities for MHRA, TGA, SFDA. Provide International (outside North America) regulatory submissi...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
Company: Yoh Electronic Submission Specialist needed for a contract opportunity with Yoh's client located in Berkeley Heights, NJ. The Big Picture - Top Skills You Should Possess: - Regulatory submissions - IND, NDA, MAA, CTD - Electronic Document Management Systems What You'll Be Doing: - Support Regulatory Affairs personnel in the coordination, preparation, and submission of INDS / NDAs / MAAs a...
Company: Yoh Medical Information Specialist needed for a contract opportunity with Yoh's client located in Woodcliff Lake, NJ. What You'll Be Doing; - The Medical Information Specialist is responsible for meeting the medical information needs of external customers and internal business partners as it relates to the company's products. - He/she will contribute to the development of high-quality Med...
Long term contract opportunity with a fast-growing international pharmaceutical company! Team-oriented work environment! The Medical Information Specialist is responsible for meeting the medical information needs of external customers and internal business partners as it relates to the company’s products. He/she will contribute to the development of high-quality Medical Information deliverables wi...
Long term contract opportunity with a fast-growing international pharmaceutical company! Team-oriented work environment! The Medical Information Specialist is responsible for meeting the medical information needs of external customers and internal business partners as it relates to the company’s products. He/she will contribute to the development of high-quality Medical Information deliverables wi...
Our client, a large pharmaceutical company, is currently seeking a BIOSTATS SPECIALIST. This job will have the following responsibilities: Work under the direction of Medical Affairs Statistics Disease Lead. Actively provide statistical support to the Medical Affairs Department. Provide statistical support for publications, presentations, posters at medical meetings and any other requests not cove...
Our client, a large pharmaceutical company, is currently seeking a BIOSTATS SPECIALIST. This job will have the following responsibilities: Work under the direction of Medical Affairs Statistics Disease Lead. Actively provide statistical support to the Medical Affairs Department. Provide statistical support for publications, presentations, posters at medical meetings and any other requests not cove...
Job Number: 420980 Biostats Specialist CELGJP00002840 Responsibilities will include, but are not limited to, the following: Work under the direction of Medical Affairs Statistics Disease Lead. Actively provide statistical support to the Medical Affairs Department. Provide statistical support for publications, presentations, posters at medical meetings and any other requests not covered in the clin...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
Are you looking for a Clinical Research position with a large pharmaceutical company Maryland, Northern NJ and PA areas. TechData Service has multiple positions in Pharmaceutical companies in clinical research, Medical Writing, Electronic Submissions, Technical Writer, Manufacturing Tech., Accounts Payable Clerk and Biostatistics/SAS Programming positions (both home based and work on site). We can...
Are you looking for a Clinical Research position with a large pharmaceutical company Maryland, Northern NJ and PA areas. TechData Service has multiple positions in Pharmaceutical companies in clinical research, Medical Writing, Electronic Submissions, Technical Writer, Manufacturing Tech., Accounts Payable Clerk and Biostatistics/SAS Programming positions (both home based and work on site). We can...
TechData is looking for Scientist I, Scientist II, Biostatistician (on site or telecommuting), SAS Programmer/Statistical Programmer/telecommuting, CDISC programmer (remote, multiple positions as sr. or lead positions), Java Programmer (Remote), Medical Writer, Sr. Clinical Data Manager, Drug Safety Specialist for our pharmaceutical clients in Central and Northern NJ. Please see below requirements...
Any combination of skills, experience will do, please see full descriptions below. PLEASE HAVE PHARMA INDUSTRY EXPERIENCE Director * Market Access up to 170k base Senior Director, Customer Support up to 200k base Sr Dir Marketing up to 210k base Sr Dir Marketing- Cardiovascular up to 210k base Sr Dir Marketing-Cardiovascular up to 210k base Sr Director Marketing (Marketing Business Partner/Marketi...

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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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