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Raptor Pharmaceuticals
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4/14/2014
Raptor Pharmaceuticals
Novato, CA

The Manager, Document Control has overall responsibility for developing, implementing, managing and the Document Control Systems according to FDA GxP requirements, ICH GxP requirements, internal and typical pharmaceutical industry practices. •In...

4/14/2014
Raptor Pharmaceuticals
Novato, CA

The Associate Director, QA Lot Disposition is responsible for directing the quality activities required to accurately complete the review and approval of the Raptor QA document and record review for drug substance and commercial and clinical drug...

3/21/2014
Raptor Pharmaceuticals
Novato, CA

The Associate Manager/ Manager, Regulatory Affairs is responsible for supporting regulatory activities, will write and prepare IND/NDA documents, contribute to the completion of projects, assist with development programs, and ensure compliance with...

3/20/2014
Raptor Pharmaceuticals
Novato, CA

Summary Description The Quality Assurance Executive Director is responsible for leading the Quality Assurance department in accordance to cGMP regulations and internal standards. The Executive Director will provide leadership in the oversight of...

3/20/2014
Raptor Pharmaceuticals
Novato, CA

Summary Description The Senior Director Quality Control will provide oversight of developing and maintaining in-house analytical expertise for all drug substance, drug product, and bio-analytical methods. The Senior Director Quality Control will...




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