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Yoh has a longterm contract opportunity for a QA Engineer to join our client, a medical device company, in Raleigh, NC area. Job Responsibilities: Collaborate ...
Researches, writes and edits clinical reports, summarizing statistical data from clinical studies for submission to FDA / regulatory authorities and for publication ...
We currently have an excellent opportunity for a Project Manager / Project Director with a background leading clinical trials (Phase II and III) in Infectious ...
Our client, an established and expanding firm that provides consulting and contract research support to the pharmaceutical industry, is actively recruiting ...
Plan and direct the operations of an R&D department focused on: ** Developing liquid and gel formulations for customer provided entities. ** Creating analytical ...
Medical Director Internal Medicine, CRO, North Carolina Medical Director Internal Medicine: My client is one of the world's leading CROs, with global sites ...
**Job location is dependent upon experience and qualifications for the position Under minimal supervision, the Feasibility Medical Writer researches, prepares, ...
PPD is a leading global contract research organization providing drug discovery, development and lifecycle management services. Our clients and partners include ...
Seeking Phd in molecular biology or similar and at least 7 years working experience with cloning, qPCR, RTPCR, assay optimization, and nucleic acid isolation ...
1116SMH (Associate) Director Pharmaceutical Commercial Manufacturing Location: Research Triangle Park, NC Salary Range: Commensurate with Experience + Bonus ...
For your reference, we have included the original job posting below.
Director Regulatory Affairs - Medical Device - Class III
Job Number:
43360016
Company Name:
CyberCoders Pharmaceutical
Job Location:
Raleigh, NC US
Job Category:
Science & Biotech
Director Regulatory Affairs - Medical Device - Class III
This position is open as of 1/25/2012. Director Regulatory Affairs - Medical Device - Class III ••• Position is located in BEAUTIFUL Irvine, CA and we will pay for relocation ••• Are you a Director of Regulatory Affairs with Class III Medical Device experience? Are you looking for an opportunity where you can help develop and establish a growing Regulatory Affairs team? If so, I have a GREAT opportunity for you! Located in beautiful Orange County, CA, we are a rapid...