Regulatory Affairs Specialist Jobs in Jersey City, New Jersey

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18 Jersey City, NJ Regulatory Affairs Specialist jobs found on Monster.

Jobs 1 to 18 of 18
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...
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 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...
Facilitate all aspects of credentialing, including appointment and the reappointment of all professional medical/dental staff members and allied health staff pursuant to regulatory requirements and the Hospital Bylaws. Ensure privileging criteria and information is accurate and up-to-date and all necessary supporting documentation is provided. Prepare the agenda and oversee the support and record...
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...
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...
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...
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...
The Stress Testing team form an important part of the risk methodology group of UBS. The team is responsible for the on-going development and maintenance of the stress testing and scenario analysis frameworks of UBS group, UBS's legal entities and most UBS business divisions. The team has a global remit as the methodologies and analysis it produces encompasses all the relevant risk exposures of ea...
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...
Administers the installation, troubleshooting and technical solutions, of products/equipment in order to ensure and deliver the highest level of quality to the customer. Determines and recommends which products and/or services best fit the customer’s needs. Facilitates and acts as liaison between customer and Product Support Specialist or Engineering. Exhibits confident personality. Experience on...

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Regulatory Affairs Associate

Salaries

$42,000.00 - $84,700.00
Typical Salary for Regulatory Affairs Associate in Jersey City
(9 Respondents)
Source: Monster.com Careerbenchmarking Tool

Education / Training

Master's
57.1%
Bachelor's
42.9%
(7 Respondents)
Source: Monster.com Careerbenchmarking Tool

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