Senior Manager, Regulatory Affairs (Strategy and CMC)
Lake Zurich, Illinois
Job Summary The Senior Manager, Regulatory Affairs (Strategy and CMC) delivers regulatory guidance which includes strategic and CMC input in Biosimilar Development and Life Cycle Management to find smart solutions for optimized submission, ...
12d
| Job Type | Full Time |
Sr. Director, Regulatory Affairs
Lincolnshire, Illinois
Sr. Director, Regulatory Affairs Job Location(s) US-IL-Lincolnshire # of Openings 1 Job ID 2024-4181 Category Surgical Robotics Business Travel 25% Overview Find a Better Way... ...to use your skills and experience. This is the time to let ...
12d
| Job Type | Full Time |
QA Associate Director, CMC Regulatory Submission QC and Audit
Boston, Massachusetts
Vertex Pharmaceuticals Incorporated
Job Description The QA Associate Director, CMC Regulatory Submission QC and Audit, is responsible for the audit/review of all regulatory submissions in support of submission readiness for small molecule, biologics, and medical devices. This...
12d
| Job Type | Full Time |
Manager, Regulatory Compliance and Permitting
Arlington, Virginia
Company Description Founded in Denmark, Ramboll is a foundation-owned people company. We have more than 18,000 experts working across our global operations in 35 countries with thousands of experts working across 70 offices in the Americas....
12d
| Job Type | Full Time |
MEDICAL DEVICE REGULATORY AFFAIRS PROJECT MANAGER
Jacksonville, Florida
Job Details Job Location Corporate Office - Jacksonville, FL Position Type Full Time Education Level 4 Year Degree Travel Percentage None Job Shift Day Description **This will be a local remote position and you must reside within 125 mile...
12d
| Job Type | Full Time |
Cambridge, Massachusetts
How will your role help us transform hope into reality? As a recognized expert in drug substance development and manufacturing, you will enable advancement of Blueprint Medicines' clinical and commercial programs. You will be expected to co...
12d
| Job Type | Full Time |
Director, Global Regulatory Strategist (Eye Care)
Oyster Point Pharma, Inc (Delaware corp) At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers p...
12d
| Job Type | Full Time |
Senior Director-Regulatory SPM & CMC
Massachusetts
Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a differ...
13d
| Job Type | Full Time |
Senior Manager, Process Sciences
Cambridge, Massachusetts
This role is considered On-Site. Overview This position will be a part of the CMC Drug Substance Process Sciences group, leading a small team. This role will include process development, in-house non-GMP manufacturing of siRNA and process t...
13d
| Job Type | Full Time |
Director, Global Labeling Operations
The Director, Global Labeling Operations provides regulatory expertise and guidance for Regulatory labeling operations, to deliver high quality submission labeling and artwork for complex drug, device and combination products, specific ther...
13d
| Job Type | Full Time |