Regulatory Affairs Specialist Jobs in New Jersey
12 New Jersey Regulatory Affairs Specialist jobs found on Monster.
The Playtex strategic business unit, which is a division of Energizer Personal Care, is a leading manufacturer and distributor of a diverse portfolio of consumer and personal products. Playtex is focused on Feminine Care products, including Gentle Glide and Sport tampons; Infant Care products, including spill-proof cups, baby bottles, pacifiers, and Diaper Genie; Sun Care products, including Banan...
THERAKOS® is a global leader in advancing the science of extracorporeal photopheresis (ECP). For 25 years, THERAKOS® employees have pioneered new and industry leading technologies. As we look to drive the next phase of Therakos’ growth, we are seeking to expand our team with talented leaders and professionals in all functional areas. THERAKOS® offers a range of opportunities to work and grow in an...
SPARTAN SEARCH GROUP is the premier placement firm for technical and engineering positions in the Northeastern USA. With offices in Morristown, NJ and a primary focus on medical device opportunities with companies both large and small, we are in constant contact with the top tier, game-changing technical leaders in the industry. We are currently working with a very strong Medical Device company th...
PLEASE NOTE THIS IS A 6-7 MONTH CONTRACT POSITION. Skills:Regulatory Affairs Experience, Biomedical Device Experience, Negotiate Regulatory Submissions, FDA Quality Systems, ISO 13485, Writing SOPs, Product Development Processes Represents Regulatory Affairs on product lifecycle teams by actively contributing to the development and implementation of regulatory strategies. Independently prepares an...
Summary: Work within the All Americas Division (AAD) comprising Diagnostica Stago, Inc., Stago Canada Ltd., and Latin America to plan, execute and support pertinent regulatory submissions during various phases of product life cycle; assist in complaint handling with a process-driven project approach; analyze complaint data to identify unfavorable trends and contribute to effective and efficient co...
DESCRIPTION: Summary: Work within the All Americas Division (AAD) comprising the US, Canada and Latin America to plan, execute and support pertinent regulatory submissions during various phases of product life cycle; assist in complaint handling with a process-driven project approach; analyze complaint data to identify unfavorable trends and contribute to effective and efficient corrective and pre...
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 available in the following locations: East Coast: Somerville, New Jersey and West Chester, Pennsylvania California: Fremont, Menlo...
Requisition ID 11974BR Title Sr. Associate/Specialist, Reg Affairs Operations-Submissions Publisher Job Category Regulatory Affairs Job Description PURPOSE: The Regulatory Operations Senior Associate/Specialist will support the global extent of e-submissions and use of Insight Publisher and/or Novodocs for regulatory submissions in Novo Nordisk and will identify, analyze and develop technical solu...
Regulatory Operations Publishing and Submission Specialist Our client, a leading pharmaceutical company, has a high priority need in its Regulatory Affairs group for a Submissions or Senior Submissions professional in Northern New Jersey. This is a rare opportunity that offers potential for you to leverage your experience and take your career to the next level. In this position, you will play an i...
JOB SUMMARY: The Sr. Principal Specialist, in interaction with Management, is responsible for the development, implementation and management of specific audit activities and programs. These programs are designed to support stated goals for identified development activities both within the CSO Platform and to outside providers including investigators and CROs. The Sr. Principal Specialist is also r...
Job Summary: 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 responsibilities, the audits and activities require proven ability to independantly interact with all internal and external (e.g. Vendors / CRO) operational staff (e.g. Project Teams, Clinical Operations,...
Description The Ethicon Surgical Care business offers a broad range of products, platforms and technologies-including sutures, surgical staplers, clip appliers, trocars and synthetic mesh devices-that are used in a wide variety of minimally invasive and open surgical procedures. Specialties include support for treatment of colorectal and thoracic conditions, women's health conditions, hernias, can...
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Regulatory Affairs Associate
Salaries
$38,760.00 - $94,500.00
Typical Salary for Regulatory Affairs Associate in New Jersey
(109 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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©2013 Monster - All Rights Reserved U.S. Patents No. 5,832,497; 7,599,930 B1; 7,827,125 and 7,836,060 MWW - Looking for Monster Cable? - V: 2013.5.0.223-222