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Morrisville, NCFull-time Company Description Liquidia Technologies, founded in 2004, is a privately held biotechnology company located in Research Triangle Park, North Carolina. By leveraging precise fabrication techniques of the semiconductor industry, Liquidia has become the4/5/2016 Morrisville, NC Save This Job
TARIS Biomedical is a unique therapeutically-focused urology company developing drug-device combination products for the treatment of genitourinary diseases. This individual will provide leadership and expertise for regulatory activities that support assigned TARIS? pipeline3/12/2016 Lexington, MA Save This Job
Department: Regulatory Affairs Position Type / FLSA Status: Full Time / Exempt Location: Emeryville, CA Position Summary This position is primarily responsible for developing, coordinating and implementing regulatory strategies for new product development registrations,4/19/2016 Emeryville, CA Save This Job
Job ID87 OverviewResponsible for independently developing regulatory strategy and filings (e.g. Annual Reports, Supplements, CBEs (Changes Being Effected), Protocols, etc.), providing critical review of CMC (Chemistry, Manufacturing, and Controls) and clinical submissions,4/4/2016 Blue Ash, OH Save This Job
We are seeking a highly experienced candidate with an advanced medical and science degree, preferably in oncology, to lead our effort into the clinical development of the company immunodiagnostic assay pipeline, and provide strategic guidance in regulatory affairs and compliance.3/5/2016 Emeryville, CA Save This Job
ID 2016-1020 # of Openings 1 Job Locations US-MD Posted Date 2/4/2016 Category Other More information about this job: Overview: Leads and drives Quality System function and associated activities Proactively provides guidance to the functional teams to ensure Quality System2/8/2016 Baltimore, MD Save This Job
Location: Schaumburg, Illinois, USA Senior Associate Operations, Regulatory Affairs Department: Regulatory Affairs Reports To: Associate Director, Regulatory Affairs Job Summary / Overview: Responsible for the support of Pre and Post approval regulatory affairs activities as4/6/2016 Schaumburg, IL Save This Job
Location: Schaumburg, Illinois, USA Associate Operations, Regulatory Affairs Department: Regulatory Affairs Reports To: Associate Director, Regulatory Affairs Job Summary / Overview: Responsible for the support of Pre and Post approval regulatory affairs activities as3/7/2016 Schaumburg, IL Save This Job
Company Overview Relypsa, Inc. is a late clinical-stage pharmaceutical company leading the discovery and development of novel non-absorbed polymeric drugs for important applications in cardiovascular and renal diseases. Relypsa's lead product candidate is patiromer, a3/9/2016 Redwood City, CA Save This Job
Req Id 3421 - Posted 03/25/2016 - United States - Massachusetts - Cambridge - Regulatory Affairs The Director, Regulatory Affairs, REMS, is responsible for providing strategic and operational leadership for the Risk Evaluation and Mitigation Strategies (REMS) for the Company?s4/14/2016 Cambridge, MA Save This Job
The Associate Director/Director, Regulatory Operations reports to the VP Regulatory Affairs. This position is responsible for the oversight and management of day-to-day Regulatory submissions to Global Health Authorities (i.e., FDA, Health Canada, EMEA, SFDA, etc.). This5/3/2016 San Francisco, CA Save This Job
SENIOR DIRECTOR, GLOBAL REGULATORY AFFAIRS We have an exciting newly created opportunity for an outstanding Head of Regulatory Affairs in our dynamic, successful and fast growing pharmaceutical company. ABOUT ENANTA Enanta Pharmaceuticals is a research and development-focused4/18/2016 Watertown, MA Save This Job
Discovery Cambridge, MA, United States Director of Regulatory Affairs, Discovery Merrimack is a fully integrated biopharmaceutical company that views cancer as a complex engineering challenge. Through systems biology, which brings together the fields of biology, computing and4/13/2016 Cambridge, MA Save This Job
COMPLIANCE Department: Finance Job Location: South San Francisco Cytokinetics is a late-stage biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators as potential treatments for debilitating diseases in which muscle4/5/2016 South San Francisco, CA Save This Job
Location:Pleasanton, California DESCRIPTION Summary: Provide leadership over the Regulatory Affairs function to ensure the departmental activities align with overall Company goals and strategies. Responsible for establishing and administering sound Regulatory policies,3/21/2016 Pleasanton, CA Save This Job
Director of Quality AssuranceEmail inShare Location: East Windsor, NJ Aprecia is a specialty pharmaceutical company committed to transforming customers' experience with highly prescribed high-dose medications. Built upon our proprietary three-dimensional printing (3DP)5/4/2016 Blue Ash, OH Save This Job
Company Overview Relypsa, Inc. is a biopharmaceutical company focused on the discovery, development and commercialization of polymeric medicines for patients with conditions that are often overlooked and undertreated and can be addressed in the gastrointestinal tract. The3/9/2016 Redwood City, CA Save This Job
Reporting to the Senior Director of Chemical Development, the successful incumbent will work on all process chemistry aspects of new small molecule pharmaceuticals Responsibilities will include: Assisting in oversight of CMO activities related to technology transfer, development,5/3/2016 San Francisco, CA Save This Job
Location:USA - CA Company Order Number:397 # of openings:1 Description About the Company TeraRecon is the largest independent, vendor neutral medical image viewing solution provider with a focus on advanced image processing innovation. TeraRecon iNtuition and iNteract+ solutions3/19/2016 San Mateo, CA Save This Job
The Manager / Sr. Manager of Regulatory Operations is responsible for oversight and hands-on day-to-day support of Regulatory Operations. This role will actively participate in Paper and Electronic dossiers for submissions to Global Regulatory Health Authorities (i.e., FDA,5/3/2016 San Francisco, CA Save This Job