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Regulatory Affairs Specialist Jobs

312 jobs

RESPONSIBILITIES: Kforce has a client that is searching for a Senior Regulatory Affairs Specialist in Hazelwood, MO. The Senior Regulatory Affairs Specialist responsibilities encompass the support of US FDA and international product registrations. The regulatory activities include, but are not limited to: Prepare, submit and maintain product specific electronic dossiers per FDA requirements Pa...
A growing and exciting global leader in The Consumer Packaged Goods Industry is looking for a Regulatory Affairs Specialist. Responsibilities: Ensure global compliance of products Conduct raw material and formula reviews Review and approve claims, packaging/labeling and marketing communication materials. Work cross-functionally with RD&E, Sales, Marketing, etc. Represent RD&E on cross functi...
Regulatory Affairs Specialist Piper Clinical Solutions is seeking an Regulatory Affairs Specialist to work as part of a medical devices company in Raleigh / Durham / Chapel Hill area. Qualifications for the Regulatory Affairs Specialist The Regulatory Affairs Specialist will be responsible for assisting regulatory affairs functions through interfacing with various departments to organize docume...
The International Regulatory Affairs Specialist role is a developed position with a highly profitable industry leader in the medical device, health care, and consumer goods industry. Our client is looking for an experienced Regulatory Affairs Specialist to support the legal department and litigation/compliance for the company in regards to international business across Europe and the Middle East. ...
REGULATORY AFFAIRS SPECIALIST/MEDICAL DEVICE INDUSTRY Palo Alto, California (Peninsula) A growing and reputable Medical Device centered Corporation is seeking a Regularity Affairs Specialist for a start-up environment. The duration is for either a 6 month contract-to-hire OR Direct hire depending on experience. This position is responsible for product submissions, license renewals, periodic upd...
If you are a Sr. Regulatory Affairs Specialist with experience, please read on! We are located in San Jose, CA and are a major player in the Medical Device Industry. We are currently looking to hire a very experience Regulatory Affairs Specialist with 510K experience. If you have experience working in the medical device arena doing 510K work we would love the opportunity to tell you more about th...
Regulatory Affairs Specialist TEMP in US - WA - Snoqualmie Job Overview At Spacelabs Healthcare, we are on a mission - to develop innovative medical systems and services that provide patient monitoring, anesthesia delivery and ventilation, and cardiology diagnostics to clinicians and healthcare facilities around the world. Our Mission: To inspire the world to bring the best care experience to p...
Regulatory Affairs Specialist Piper Clinical Solutions is actively seeking an entry- to mid-level Regulatory Affairs Specialist to work with an international medical device company in the Raleigh-Durham (RTP) area. The Regulatory Affairs Specialist will be working on a team that supports international submissions, and will be working in-office in the RTP area. This is a 3-6 month contract opport...
Are you interested in Regulatory Affairs? Do you enjoy working in the pharmaceutical industry? I have the position for you! My client, a leader in the pharmaceutical Industry is looking for a Senior Regulatory Affairs Specialist to join their growing team. This would be an amazing opportunity to join a company that is the best in the market and truly fosters innovation in the field. This will be ...
Are you interested in Regulatory Affairs? Do you enjoy working in the medical device industry? I have the position for you! My client, a leader in the medical device industry is looking for a Regulatory Affairs Specialist to join their growing team. This would be an amazing opportunity to join a company that is the best in the market and truly fosters innovation in the field. This will be a 6 mon...
Job ID: 259461 Contract Length: 6 months Our client is looking for a Regulatory Affairs Specialist for a contract role in Andover, Massachusetts. The primary task for this Regulatory Affairs Specialist is to provide significant regulatory support for the defibrillator PMA submissions to FDA. This will involve strong collaboration with other members of the cross functional PMS team. The RA Speciali...
Contract Regulatory Affairs Specialist - Seattle, WA Requisition ID: 5842 Location: USA, Washington, Seattle Employment Duration: Temp Full time Description Founded in 1989, Natus Medical Incorporated is a leading manufacturer of medical devices and software and a service provider for the Newborn Care, Neurology, Sleep, Hearing and Balance markets. Natus products are used in hospitals, cli...
Senior Regulatory Affairs Specialist - Seattle, WA Requisition ID: 6127 Location: USA, Washington, Seattle Employment Duration: Regular Full time Description Founded in 1989, Natus Medical Incorporated is a leading manufacturer of medical devices and software and a service provider for the Newborn Care, Neurology, Sleep, Hearing and Balance markets. Natus products are used in hospitals, cl...
The Regulatory Affairs Specialist will be responsible for the preparation of regulatory submissions required to market new or modified medical devices and in vitro diagnostic devices in both domestic and international clinical markets. This responsibility entails development, execution and management of procedures and systems designed to ensure that the product development process, including clini...
The Regulatory Affairs Specialist Post-Market is responsible for regulatory review of post-market changes to on-market medical and laboratory products marketed by BDDS.This associate will provide regulatory guidance to change control review boards and will support sustaining engineering teams as assigned concerning regulatory requirements for notification, submission and compliant implementation o...
The Regulatory Affairs Specialist will be responsible for the preparation of regulatory submissions required to market new or modified medical devices and in vitro diagnostic devices in both domestic and international clinical markets. This responsibility entails development, execution and management of procedures and systems designed to ensure that the product development process, including clini...
Looking to fill a position as a Quality & Regulatory Affairs Specialist at a Medical Device company located in Portland, Oregon. Primary Responsibilities: Plan, coordinate and execute risk management activities in accordance with the requirements of ISO 14971 and applicable regulations, standards and / or regional requirements (e.g. ISO 13485, FDA, MDD, CMDR) Ensuring implementation, alignment ...
We are a leading pharmaceutical company who needs a talented regulatory affairs specialist asap! Top Reasons to Work with Us - Competitive Base Salary and Benefits - Leading global supplier of high quality active pharmaceutical ingredients (APIs) for over three decades - Backed by a $317M Pharma Giant What You Will Be Doing 1. Assists in the preparation of new, and helps maintain existing Dr...
Our client, a leading fortune company is looking for an Associate Regulatory Affairs Specialist in their organization. This is a 6 months contract position and is located in Irvine, CA Description/Comment: Support regulatory compliance throughout the organization by performing the required activities that assure compliance with domestic and international regulations. Help refine and maintain sy...
ROLE: This Position reports to the Associate Director of Global Regulatory Affairs and this contract position is located in Irvine, CA. EXPECTATIONS: The incumbent: Assists in developing global regulatory strategies for new, modified medical devices and line extensions. Reviews device labeling, marketing materials, UDI related activities for compliance Reviews product and manufacturing chang...