Fri, 06 Nov 2009 13:13:00 GMT
Knowledge of cGMP/GLP Regulatory Requirements.
Review of documentation for conformance to established procedures and regulatory guidelines.
Conduct daily auditing, inspecting and reporting on quality functions.
Perform QA functions in support of cGMP manufacturing as necessary.
Ensure that work conforms to appropriate regulatory requirements, including SOP’s, US FDA and US EPA Good Laboratory Practices (GLP) and US FDA current Good Manufacturing Practices (cGMP).
Candidates must live local to the Norwood MA area and be a US Citizen or Permanent Resident Green Card Holder
Email resume as a word attachement to: jobs@cwsciences.com
Commonwealth Sciences, Inc.
http://www.cwsciences.com
Location: Norwood
Principals only. Recruiters, please dont contact this job poster.
Please, no phone calls about this job!
Please do not contact job poster about other services, products or commercial interests.
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