Job Search Results - Biospace
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2/11/2016
Biotecher
Orange County / Irvine Area, CA

If you have 3 to years' pharmaceutical industry experience, have an engineering degree, and are a thinker who in into the science of pharmaceutical process engineering, then we want to speak with you. This is an opportunity to take on a management...

2/11/2016
BioSpace Recruiting
Urbandale, IA

Test

2/11/2016
Stemcentrx, Inc.
South San Francisco, CA

SAS® programming to provide programming support for multiple oncology studies in multiple stages of clinical development. This role will interact with Biostatistics, Clinical Data Management, Medical Writing, Clinical Information Systems, Clinical...

2/11/2016
Seattle Genetics, Inc.
Bothell, WA

Seattle Genetics Seattle Genetics is an equal opportunity employer. All qualified applications will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability...

2/11/2016
Zintro
Tacoma, WA

Zintro is looking for candidates on behalf of our client. This is an opportunity for a dedicated medical professional to join our mission of protecting human research subjects as a Board Chair in our Puyallup, Washington location.PLEASE...

2/11/2016
Zintro
Cambridge, MA

Zintro is looking for candidates on behalf of our client. We are seeking a Quality Systems Specialist for a Full-time position based in Cambridge, MA. ***To be considered for this job, Candidates MUST reply with a brief summary of their...

2/11/2016
Zintro
Bothell, WA

Zintro is looking for candidates on behalf of our client. Senior GMP Systems Analyst: This is a full-time employment opportunity onsite in Seattle Washington, USA.***Job Summary***:Designs, implements, and maintains in-house GMP...

2/11/2016
Zintro
Southborough, MA

Zintro is looking for candidates on behalf of our client. This is a full-time employment opportunity onsite in Southborough, MA.**As a Manager, Clinical and Regulatory Medical Writing You Will:- Implement project-specific strategies and...

2/11/2016
Shire Pharmaceuticals Group
Lexington, MA

Primary RoleUnder the direction of the line manager, the Associate Director is responsible for supporting the oversight and management of the Global CMC Regulatory Submissions for Development submissions (IMPD/CTA/IND), Marketing Applications (NDA,...

2/11/2016
Shire Pharmaceuticals Group
Lexington, MA

Primary RoleThe individual will be a key contributor within a group responsible for performing purification process development, including timely completion of small-scale experiments, scale-up, technology transfer and GMP floor support for programs...