Get Our FREE Industry eNewsletter


Refine Job Search:

Clear All Selections
Selected Area of Expertise
Development

Clear All Selections

Your search returned 13 jobs



10/23/2014
SillaJen, Inc.
San Francisco, CA

SillaJen, Inc., headquartered in Seoul, with laboratory facilities in Busan, South Korea and offices in San Francisco, USA, is an R&D company specializing in the translational and clinical development of complex biologics. The company is comprised...

10/23/2014
AuraSense Therapeutics
Chicago, IL

AuraSense Therapeutics (AST) is a biopharmaceutical company developing first-in-class therapies based upon its proprietary Spherical Nucleic Acid (SNA) gene regulation and immune modulation strategies. AST is leading the translation of SNA constructs...

10/23/2014
Ultragenyx Pharmaceutical Inc.
Novato, CA

Why Join Us Ultragenyx is a clinical stage biotechnology company committed to bringing to market novel products for the treatment of rare and ultra-rare diseases with an initial focus on serious debilitating metabolic genetic diseases. Founded in...

10/22/2014
Applied BioCode, Inc.
Santa Fe Springs, CA

Applied BioCode is a privately held biotechnology company with headquarters in Santa Fe Springs, California. Applied BioCode manufactures and markets Barcoded Magnetic Beads (BMB) and detection systems for the development of highly multiplexed...

10/21/2014
wondfo USA
San Diego, CA

Essential Duties and Responsibilities - Build a regulation approved R&D lab from the ground up. - With market-oriented concepts, develop new products and design experiments based on scientific research results until they are successfully launched...

10/21/2014
Ataxion Inc.
Cambridge, MA

Ataxion, Inc. is a discovery-stage biopharmaceutical company developing novel therapies for rare, debilitating, and underserved neurologic diseases. Our lead program is focused on a group of orphan genetic disorders termed hereditary ataxias. These...

10/17/2014
HTG Molecular Diagnostics
Tucson, AZ

Essential Duties: • Responsible for creating required documents such as SOPs, reagent manufacturing work instructions, incoming material specifications and performance verifications. • Analyze procedures and production methods to improve quality,...

10/17/2014
Xellia Pharmaceuticals
Raleigh, NC

POSITION SUMMARY Responsible for supervising the activities of Environmental Monitoring technicians and scientists that provide production coverage on all shifts. Responsible for effectively hiring, developing, coaching, counseling, managing and...

10/15/2014
Shire Pharmaceuticals Group
Lexington, MA

Primary Role: The Head of Nonclinical Regulatory Submissions is responsible and accountable for the planning, tracking, compilation and delivery of all nonclinical documents for regulatory submissions. The successful group leader is expected to...

10/10/2014
NewLink Genetics
Ames, IA

POSITION SUMMARY The Purpose of this position is to develop and validate robust analytical test methods in the Tumor Immunology Department to support the testing of Clinical Samples. In addition, analytical methods to test for the Quality Attributes...