Regulatory Affairs Specialist Jobs
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Full-Time | Pay: $0 - $100k/year
Senior Regulatory Affairs Specialist The Senior Regulatory Affairs Specialist is responsible for preparing regulatory and technical documentation to support and obtain regulatory approvals and maintain regulatory compliance. Responsibilities Prepare regul...
Cherry Hill, NJ
Kelly Scientific is seeking a Regulatory Affairs Specialist to join a well-known biotech in the Bothell, WA area! The primary focus of the Specialist in Regulatory Affairs role will be to provide support for the regulatory affairs department with products...
The Regulatory Affairs Specialist I at Cook Inc. is responsible for the planning and preparation of submissions to obtain regulatory approvals for new and modified Class I, II, III and IV medical devices in specific markets. In addition to submissions, th...
Sarah Cannon is the research arm of HCA’s global cancer enterprise. Focused on advancing therapies for patients, it is one of the world’s leading clinical research organizations conducting community-based clinical trials in oncology, cardiology and orthop...
Sarah Cannon Research Institute Clinical Operations
3322 West End Avenue
Aerotek Scientific is searching for a Regulatory Affairs Specialist with a Medical Device company here in the Jacksonville, FL area. Qualifications: * Either a Bachelor's degree with 5+ years' experience in regulatory affairs OR * Bachelor's degree with m...
Requisition ID: 35501 Title: Regulatory Affairs Specialist Division: Arthrex, Inc. (US01) Location: INC- Naples, FL (US08) Main Objective: Supports Regulatory Affairs activities for Arthrex, Inc. Essential Duties and Responsibilities: With minimal supervi...
The Regulatory Affairs Specialist assists in writing, submitting and gaining clearance for 510(k) submissions and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products. This position entails develop...
Valley Forge Business Center
2560 General Armistead Ave.
The QTI Group has partnered with a leading pharmaceutical company to recruit for an Regulatory Affairs Specialist to join their Quality team. This individual will help prepare and maintain regulatory agency submissions and maintain required compliance rep...
Johnson & Johnson Medical Devices, a member of Johnson & Johnson family of companies, is currently recruiting for a Regulatory Affairs, Specialist III located in Cincinnati, OH. Less than 10% travel is required. Johnson & Johnson Medical Devices is curren...
Pharmaceutical company seeking a Regulatory Affairs Specialist to join their team! Responsibilities: Preparation of more complex ANDAs, Supplements, Annual Report and responses to FDA review letters/requests for additional information in support of existi...
Costa Mesa, CA
Central Garden & Pet (Central), is a leading innovator, marketer and producer of quality branded products for the lawn and garden and pet supplies markets. The Regulatory Affairs Specialist will assure FDA, state, and international government documentatio...
Senior Regulatory Affairs Specialist Wilmington, DE Opportunity This position assists Regulatory Affairs management with providing consultation and guidance to senior leaders throughout M&T with respect to regulatory and examination activity impacting the...
People are at the center of who we are and what we do. Are you seeking… A culture defined with the help of your voice? Recognition for your talent and continued growth opportunity? Upfront tuition assistance (eligible day one of employment)? A dynamic ben...
Additional Job Description The Senior RA Specialist will provide regulatory support on a range of medical devices and activities which include new product introduction, post market design changes, regulatory submissions, regulatory compliance, internation...
Sr. Regulatory Affairs Specialist Education: BS Degree in Life Sciences or related field Experience: Minimum of 4+ years experience in a regulatory role from a Medical Device company “Required Skills”: Experience with European submissions is required Expe...
Looking to work for a leader in their industry? Interested in working for an employer who has never had layoffs? How many companies can say the have doubled in size over the last 2 years? This one can! This premiere employer is seeking an experienced Regu...
Full-Time | Pay: $999,999/year
The Principal Regulatory Affairs Specialist works as a high level independent contributor and is responsible for supporting the development and implementation of the overall objectives and long-range regulatory strategies that impact the introduction of n...
Must have some knowledge of regulatory experience to help review licenses that are being entered into our system by our Distribution Center. Responsibilities & Qualifications: • 1-2 years of experience in Regulatory Affairs • Strong Excel and Microsoft Of...
Environmental Specialist--TSCA Lyndhurst, NJ Regardless of where in the world you call home, the impact of Sika’s innovations are never far away. From the adhesives that make your car stronger and safer, to the concrete that makes the bridges you drive ac...
201 Polito Avenue
A strong Scientific and technological pioneering spirit drives bioMérieux development since its creation in 1963. We design innovative in vitro diagnostic solutions for our customers that initiate new forms of scientific partnerships to be at the forefron...
St. Louis, MO, United States, MO
Contract to Hire | Pay: $50k - $55k/year
Open Scientific is seeking full-time Clinical research specialist to join our regulatory and clinical research team. Experience in medical device research is preferred, but willing to train the right candidate. In this role you will: Collect and coordinat...
Boca Raton, FL
2 days ago
Full-Time | Pay: $0 - $120k/year
Job Number: 2112929 Sr. Regulatory Affairs Specialist Irvine/Costa Mesa, CA Up to 120k POSITION SUMMARY: With minimal guidance, assists with the compliance of the Quality Systems. Responsible for facilitating continuous quality improvements and ensuring r...
Costa Mesa, CA
Requisition ID 50042BR Title Specialist - Regulatory Affairs Job Category Regulatory Job Description Purpose Provide proactive support and technical assistance to more experienced regulatory personnel. Identify issues and inform appropriate individuals. A...
Plainsboro Center, NJ
We currently are seeking a dynamic, strategic, and innovative Regulatory Affairs Specialist - Asia . This key position will be based in our corporate offices in Northridge, CA (Southern CA). For more than 45 years, Pharmavite has been a trusted leader in...
Los Angeles, CA
Specialist, Regulatory Affairs for a contract opportunity with Yoh's client located in South Athens, GA. The Big Picture - Top Skills You Should Possess: 2 or more years of experience in the pharmaceutical, biologics and/or related industries Regulatory A...
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