Job Search Results - Biospace
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Your search returned 1227 jobs



5/25/2016
Bulletproof Documentation, Inc.
Novato, CA

Responsible for the management of GxP computer validation activities for on premises and externally hosted applications. The manager will ensure computer system validation activities adhere to FDA, EMA and local regulations and guidances, ICH...

5/25/2016
Bulletproof Documentation, Inc.
Burlingame, CA

The GMP Quality System Compliance Consultant will work with global quality system teams to restructure content of the corporate standards/policies and global procedures. validation documentation. The Consultant will provide global cGMP compliance...

5/25/2016
Bulletproof Documentation, Inc.
San Mateo, CA

Scope of Work: In alignment with ongoing periodic review of the body of controlled clinical operations documentation, a technical/medical writer needed to review and revise SOPs and controlled documents to: • Meet periodic review due dates • Address...

5/25/2016
Theravance Biopharma US, Inc.
South San Francisco, CA

An Associate Director/Director in Safety Assessment designs programs for the safety evaluation of development candidates and prepares nonclinical sections of regulatory submissions. This person serves as a senior member of the department, providing...

5/25/2016
Theravance Biopharma US, Inc.
South San Francisco, CA

Theravance Biopharma is a biopharmaceutical company focused on the discovery, development and commercialization of small molecule medicines across a range of therapeutic areas. We are competitively positioned with a pipeline of internally discovered...

5/25/2016
Theravance Biopharma US, Inc.
South San Francisco, CA

The Associate Director will provide statistical leadership and technical expertise in support of post-marketing and clinical development activities for multiple therapeutic areas. The Associate Director will be responsible to provide strategic and...

5/25/2016
Theravance Biopharma US, Inc.
South San Fransico, CA

The Regulatory Affairs Professional (Director) will be responsible for the comprehensive management of regulatory aspects of the company’s development projects while actively contributing as a member of the project team(s). This position will also...

5/25/2016
Theravance Biopharma US, Inc.
South San Francisco, CA

The main job activities include working in the CMC team and other cross-functional project teams to support and enable the compound and drug product development, including designing and developing formulations and processes, optimizing and scaling up...

5/25/2016
Becton Dickinson
Menlo Park, CA

The Scientist II is responsible for assisting in the development and evaluation of new assays, enhancements to existing assays and instrument protocols. Assists in the execution of assay development experiments. Uses independent judgment to adapt...

5/25/2016
Anthera Pharmaceuticals, Inc.
Hayward, CA

- This position will report to the Senior Director, Clinical Operations - The individual will be responsible for all aspects of clinical trial materials packaging, labeling, distribution and inventory management - Coordinate packaging and labeling...