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Job: Document Control Specialist (4982228) in Palo Alto, CA
Hound Ref. code: N/A   |    posted on 01/21/2012


Summary
Job Responsibilities and Requirements: Most likely candidates are currently employed or have been employed in similar types of positions but want to be part of a paradigm-shifting company doing innovative work and gain tremendous personal and career growth. Candidates must be hard working with unfaltering determination to excel in an intense start-up environment.

Job Type
Full time
Responsibilities
Major duties will include transitioning and scaling the company document change and configuration control system; ensuring accuracy and timely release of all pre-production activities. Ensure that all document control systems adhere to applicable FDA QSR and ISO 13485 standards.
Required Skills
Understanding of and adherence to GMP, QSR and ISO practices. Issuing of part numbers. Issuing and maintaining records for laboratory notebooks. Ability to train others on the document control system a plus.
 
 
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94301, Within 50 miles of 94301

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Education and
Experience
A bachelor's degree is required. 4 plus years document control experience with emphasis in medical devices, biotech or pharmaceuticals. GMP experience; medical devices, biotechnology or pharmaceuticals. A strong knowledge of Microsoft Office a must. Good interpersonal skills and training skills; ability to work independently, and problem solve. Requires proof-reading, editing and technical writing skills. Strong technical bent to problem solve. Knowledge of DRM is a plus.
Additional
Information
For more information of this job please visit us at http://www.hound.com/gjviewjob.php?jid=4aa8fe4900f0a5a1393678545d7324f36a3fb3
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