Biotechnology Regulatory jobs in New York
Broaden your search
Refine your search
-
Biotechnology
Remove selection
- Regulatory Remove selection
-
New York
Remove selection
- New York City 3
- Rensselaer 10
- Sleepy Hollow 1
- Tarrytown 25
Found 39 jobs
-
Director, Regulatory Affairs
Job Summary: The Director, Regulatory Affairs is responsible for regulatory affairs for specific drug development programs (pre and post market app
Top job
-
Technical Services Research Associate III
Mispro Biotech Services is seeking a Technical Services Research Associate III for its South San Francisco location. The candidate will be...
Top job
-
Employment Lawyer
We are looking for an Associate General Counsel, Employment, to join us in our mission to design drugs and materials to improve human health and incre
-
Sr. Sourcing Mgr., Pre-clinical Studies, Research Svcs. & Collab.
The Senior Manager Sourcing will be responsible to support and assist in the development of the Category Management strategy by gathering and anticipa
-
Manager, Regulatory Submission Project Management
Summary Responsible for project management of submission deliverables such as INDs and amendments, CTAs and amendments, BLAs and amendments/supplement
-
-
TEMP - Senior Manager, GPS CERM
The Senior Manager Case Management is responsible for proactively managing routine Vendor Management and Case Processing results and activities in acc
-
Associate Director, Vendor and Relationship Management
The Associate Director of Global Clinical Operations, Vendor & Relationship Management will be Responsible for leading integration projects for select
-
Manager Regulatory Affairs - Combination Products
Leads combination product regulatory activities, including device development activities, protocol reviews, leading/managing Health Authority (HA) cor
-
Senior Specialist, Regulatory Affairs CMC
Act as the CMC Regulatory representative for a subset of programs at the IOPS facility. Evaluate proposed changes to IOPS documents and procedures to
-
CMC Regulatory Sciences Specialist-Post Approval Commercial Submission
Summary: Responsible for providing Chemistry, Manufacturing, and Controls (CMC) support across Regeneron's sites. Routine activities include dossier
-
Manager, CMC Regulatory Affairs
This position involves utilizing a proven understanding of CMC elements and regulatory requirements to support, and provide guidance to, the Industria
-
Temp Sr Project Associate - Research Program Management
We are looking for a Temporary Senior Project Associate to join the Research Program Management Team. Using prior research and project management know
-
Associate Director, Compliance Counsel
In this newly built role at Regeneron, the Associate Director, Compliance Counsel will work on investigations to ensure compliance with all laws, regu
-
Associate Director, External Manufacturing Compliance
We are currently looking to fill an Associate Director External Manufacturing Compliance position. This position will supervise a group that supports
-
Associate Manager, Regulatory Affairs
The Associate Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects related to
-
Quality Compliance Specialist (Complaints)
We are currently looking to fill a Quality Compliance Specialist (Complaints) position. This position maintains site compliance of operations focused
-
Senior Toxicologist
We're looking to hire a Senior Toxicologist to join us in our mission to discover and develop drugs that improve human health and materials that incre
-
CMC Regulatory Sciences Specialist
Summary: Responsible for providing Chemistry, Manufacturing, and Controls (CMC) support across Regeneron's sites. Routine activities include dossier
-
CMC Regulatory Sciences Specialist
We are currently looking to fill a CMC Regulatory Sciences Specialist. Regeneron successfully manufactures a range of biopharmaceuticals for patients
-
Associate Director, Regulatory Operations- RIM
Accountable for leading, developing, and mentoring members of the RIM Process team, which includes overseeing managers and staff who are responsible f
-
Manager, Regulatory Submission Project Management
Responsible for project management of submission deliverables such as INDs and amendments, CTAs and amendments, BLAs and amendments/supplements, MAAs
-
Manager, Regulatory Publishing
Summary: Responsible for leading Regulatory Publishing staff who format and publish electronic documents, build Regulatory submission deliverables suc