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Job (this posting is now closed/inactive)


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General Information

(3645095)

Job title: Quality Systems Manager, Document Control and Training
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Job location: Durham, NC  27713 United States
Requisition code: 613962
Date posted: 07/31/2017
Compensation:
Job category:Quality Control
Employment type:Full time
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Job Description


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The Quality Systems Manager will be responsible for managing the entire document lifecycle including document issuance, format review, routing documents for review and approval, scanning and filing documents in the Master Control EDMS and maintaining hard copy original files as applicable within a fast paced development and manufacturing environment.

Specifically focused on establishing a complete and accurate index of Novan documents maintained by the Quality organization. Maintaining paper and electronic files in the Company's quality document management system in accordance with Company document lifecycle policies and procedures, federal regulations, and audit requirements. Managing GxP retention and archival schedule as well as off-site storage vendor to archive and retrieve documents as necessary. And leading the implementation and company-wide training efforts in support of cGMP activities.



The Quality Systems Manager will be responsible for managing the entire document lifecycle including document issuance, format review, routing documents for review and approval, scanning and filing documents in the Master Control EDMS and maintaining hard copy original files as applicable within a fast paced development and manufacturing environment.

Specifically focused on establishing a complete and accurate index of Novan documents maintained by the Quality organization. Maintaining paper and electronic files in the Company's quality document management system in accordance with Company document lifecycle policies and procedures, federal regulations, and audit requirements. Managing GxP retention and archival schedule as well as off-site storage vendor to archive and retrieve documents as necessary. And leading the implementation and company-wide training efforts in support of cGMP activities.

Ideal candidate will have worked within both small and large scale environments and able to work independently with influence to diverse functions in organization.


For more information, or to apply now, you must go to the website below. Please DO NOT email your resume to us as we only accept applications through our website.

https://www.applicantpro.com/j/613962-43980
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Job Requirements


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