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Manager, Regulatory Affairs International Jobs

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Manager, Regulatory Affairs

Sagent Pharmaceuticals

Location: Schaumburg, IL, USA Manager, Regulatory Affairs Department: Regulatory Affairs Reports To: Sr Manager, Regulatory Affairs AND/OR Associate Director Regulatory Affairs Job Summary / Overview: The role is primarily responsible for the management and support of Pre

7/4/2015  Schaumburg, IL  Save This Job

Senior Manager, Regulatory Affairs

Relypsa

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, a

8/5/2015  Redwood City, CA  Save This Job

Manager, Regulatory Affairs (EMEA) (1241)

Aegerion Pharmaceuticals, Inc.

The Regulatory Affairs Manager will be responsible for the preparation of CTDs and associated filings in the EU, and will also support international filings as needed. The incumbent will be responsible for managing, evaluating and completing regulatory projects consistent with

8/11/2015  Cambridge, MA  Save This Job

Group Manager, Regulatory Affairs

Globus Medical

Location:Audubon, PA Job Code:GMRAKB0415 Description The Group Manager, Regulatory, is responsible for preparing, submitting and gaining approval of 510(k), IDE, and PMA submissions to the U.S. Food and Drug Administration (FDA) for class II and class III products, and to

7/12/2015  Audubon, PA  Save This Job

Regulatory Affairs Manager (15-585)

MacroGenics

Job Code: 15-585 Location: Rockville, MD Applicants must meet the following requirements: Minimum of Bachelor?s degree in scientific discipline; advanced degree desirable Minimum of 5 years of Regulatory Affairs experience with at least two years in industry, preferably with

8/21/2015  Rockville, MD  Save This Job

REGULATORY AFFAIRS MANAGER

ViewRay

Position Goal: Manage US and international Regulatory Affairs submissions to achieve ViewRay business goals. Job Specifics: Candidate must be able to personally prepare submissions as well as strategize submission strategies and organizational structure Develops and maintains

9/2/2015  Mountain View, CA  Save This Job

Quality Systems Manager

High Throughput Genomics

Job Location Tucson, Arizona Essential Duties Responsible for the maintenance and improvement of key Quality systems and processes as well as insuring those quality requirements are defined and met during design, development and release to manufacturing. The incumbent will work

7/20/2015  Tucson, AZ  Save This Job

Quality Assurance Manager (701)

Aegerion Pharmaceuticals, Inc.

The QA Manager is responsible for oversight of selected quality systems and contract manufacturing (CMO), packaging and testing activities. Act as primary quality contact/liaison with CMO quality organizations. Serves as product quality representative on cross functional project

8/11/2015  Cambridge, MA  Save This Job

Manager, Clinical Operations

Acceleron Pharma

About Acceleron: Acceleron is a clinical stage biopharmaceutical company focused on the discovery, development and commercialization of novel protein therapeutics for cancer and rare diseases. The company is a leader in understanding the biology of the Transforming Growth

7/25/2015  Cambridge, MA  Save This Job

Manager, Pharmacovigilance

Acceleron Pharma

About Acceleron: Acceleron is a clinical stage biopharmaceutical company focused on the discovery, development and commercialization of novel protein therapeutics for cancer and rare diseases. The company is a leader in understanding the biology of the TGF--- protein

7/25/2015  Cambridge, MA  Save This Job