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Resumes 41 - 49 of 49 |
Towson, MD
... Generation and maintenance of QC reports and assisting in planning and documentation of CAPA. . Performing quality checks on internal and external study database to ensure compliance with protocol requirements. . Coordinating high-level meetings and ...
- 2014 Jan 31
Laurel, MD
... conduct risk assessments, qualify suppliers, and improve quality system • Provided subject matter expertise for CAPA and complaint handling processes • Oversaw process changes for components, manufacturers and packaging contractors KATHERINE M. ...
- 2013 Oct 24
Silver Spring, MD
... Experience in SOP development, CAPA process, research protocol development, IRB, GLP, GCP, cGMP (Part 210/211), USP, LIMS, ISO standards, statistical analysis with project management expertise, FDA and ICH regulatory experience, effective oral and ...
- 2013 Jun 14
Baltimore, MD
... Leading and investigating quality issues including that may arise, reporting them to management, implementing corrective action and preventive action (CAPA) and identifying departmental strengths and weaknesses. Ensure compliance with quality system ...
- 2013 Feb 22
Washington, DC
... Data forwarding systems5,12, 22,23, 25,46, 59 are used when Mathie et al.,22,23, 25 Wilson et al.,12,59 and Prado et al.43,44 have each designed more complex systems, capa- the weight of the wearable system is a key factor, as a data storage or a ...
- 2012 Nov 21
Elkridge, MD
... Led and reviewed investigations, represented Logistics for customer audits, and held responsibility for warehouse-related CAPA strategies and plans. aa Achieved 100% satisfaction rating from pharmaceutical customers based on their vendor management ...
- 2012 Nov 13
Gaithersburg, MD, 20878
... Management of Deviations, CAPA, Biotracker, Change control, Biorepository, Regulatory activities, FDA, ISO guidelines etc Interaction and management of contractors to assure quality and regulatory compliance, RFI, RFP writing and helping BD sales. ...
- 2012 Feb 14
Linthicum Heights, MD, 21090
... Performed CAPA, Risk Assessment, GAP Analysis and GxP Criticality Assessment. . Experience in Manual and Automation Testing. Experience with HP tools like QTP and Quality center. Involved in Defect Tracking and Defect Management. . Experience in ...
- 2010 Oct 19
Washington, DC, 20011
... of FDA's 21 CFR 210/211, Validation Master Plan Development and Review, IQ,/OQ,PQ requirements for process equipment and utilities, Process Validation, Deviation investigations and CAPA, Change Control EXPERIENCE Kymanox, Inc., Cary, NC. ...
- 2010 Sep 29