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8/28/2014
Verenium Corporation
San Diego , CA

This role is responsible for prosecution of part of the enzyme patent portfolio of GVF/N at the San Diego site (Verenium) under the oversight of a senior patent agent (IP Manager for Enzymes). The San Diego site has been designated as a global R&D...

8/28/2014
Verenium Corporation
jSan Diego , CA

Are you a self-starter that thrives in team environments? Do you enjoy leading a team into success? Are you able to prioritize multiple projects and tasks to accomplish goals on time? Is this the type of challenge you are looking for in your next...

8/28/2014
Verenium Corporation
San Diego , CA

Are you a self-starter that thrives in team environments? Do you enjoy leading a team into success? Are you able to prioritize multiple projects and tasks to accomplish goals on time? Is this the type of challenge you are looking for in your next...

8/28/2014
Vertex
Boston, MA

The Lead Quality Assurance Specialist- GMP works independently on multiple complex projects and takes a lead role in the design and execution of new projects and systems.  The Lead adapts to new and multiple projects, effectively ensuring...

8/28/2014
Vertex
Boston, MA

The Sr. Director / VP of Business Development will work with the Head of Business Development to revise Vertex’s outreach strategy and will ultimately be responsible for executing that strategy. This will involve a formalized approach to the...

8/28/2014
Vertex
Boston, MA

The Associate Director/Senior Manager, Clinical Documentation is responsible for developing and managing the standards, processes and tools to ensure the quality, completeness, and inspection readiness as well as ongoing stewardship of the Trial...

8/28/2014
Vertex
Boston, MA

Vertex Pharmaceuticals is seeking an Associate Director/Director of Program Management with proven success managing mid to late stage drug development programs.  This position will report to the Senior Director of R&D Program Management and...

8/28/2014
Vertex
Boston, MA

The Quality Lead- GMP (Post Marketing) is responsible for conducting and monitoring internal GMP activities in support of Quarterly Trending, Stability Monitoring and Product Complaints. *    Demonstrates broad and deep...

8/28/2014
Roche Molecular Diagnostics
Pleasanton, CA

Adhere to all procurement policies and procedures and ensure compliance. Implement supply chain strategies and plans consistent with overall department and corporate strategic direction in all day-to-day activities.  Responsible for maintaining and...

8/28/2014
Roche Molecular Diagnostics
Pleasanton, CA

The selected Manager of Regulatory Affairs will be expected to perform the following:Manages regulatory responsibilities associated with the development, support, and manufacturing of the ompany’s Point of Care (PoC) medical device products...