Hello Everyone, Greetings of the day. This is Vydehi from Intellectt Inc. We currently have an opening for a Regulatory Affairs Analyst with one of our medical device clients. …
Job Title Principal Regulatory Affairs Specialist Job Description Principal Regulatory Affairs Specialist- Software & Artificial Intelligence (U.S. Hub Based) The Principal R…
Associate Director, Regulatory Affairs - Boston, MA - Permanent Proclinical is seeking a strategic regulatory leader to join a renowned biotech. This is a permanent position loca…
SENIOR REGULATORY AFFAIRS SPECIALIST - Digital Technologies The Senior Regulatory Affairs Specialist will play a key role in launching new products and sustaining the current pro…
Performs full-range of regulatory functions required for Global product registrations, new product development, and internal documentation review for assigned strategic business un…
The Regulatory Affairs Specialist is responsible for identifying, evaluating, and ensuring compliance with all applicable laws, regulations, and standards. The Regulatory Affairs…
Overview The Director, RA CMC Combination Products will work cross-functionally to lead development and implementation of global combination product/Medical Devices regulatory st…
Job Title: Senior Software Engineer Location: Bedford, Massachusetts Company Overview: [Company Name] is a leading medical device company dedicated to advancing healthcare th…
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed…
Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chron…
Company Overview: Our client is a cutting-edge medical device company dedicated to revolutionizing healthcare through innovative technology solutions. Their mission is to improve p…
The Regulatory Affairs Intern will support the Regulatory Affairs team in daily tasks, projects, and FDA submission activities including: Assist in drafting, organizing, and editi…
You are motivated by working alongside a team filled with subject matter experts that will help you learn and grow… You wake up every day and do what you do … because patients …
Job Description: The Regulatory Affairs Intern will support the Regulatory Affairs team in daily tasks, projects, and FDA submission activities including: Assist in drafting, or…
Job Description The head of the device development group is responsible for the development of state-of-the-art drug delivery systems that have the potential to transform the way…
I – JOB INFORMATION Job Title: Digital Device Quality Expert Reports to: Digital Quality Lead, Health Solutions Department Name: Digital Quality Operations Location Cambrid…
The Clinical Research Resources Office (CRRO) is an office under the Human Research Protection Program (HRPP), which is a shared program of Boston Medical Center and BU Medical Cam…
The Clinical Research Resources Office (CRRO) is an office under the Human Research Protection Program (HRPP), which is a shared program of Boston Medical Center and BU Medical Cam…