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Resume alert |
Resumes 1 - 10 of 103 |
Archdale, NC, 27263
... Provided support prior and during internal and external regulated quality management systems ISO/FDA audits on an as needed basis. Coordinated the maintenance of records including, but not limited to Document Change Request in the documentation ...
- May 23
Greensboro, NC
... Field Quality Support Manager — Immunotek Biocenters July 2018 - July 2023 ● Lead Internal Audits and prepared centers for Regulatory Audits (FDA, CLIA, PPTA) ● Monitored employee performance through Data Analysis utilizing Power BI ● Reviewed ...
- May 15
Reidsville, NC
... Implement training for DOT, MDSAP and FDA compliance. Maintain training records for audits. Secure and maintain document control for patient/ client privacy. Investigate/Respond to client issues and concerns in a timely manner. Cycle count daily for ...
- May 14
Greensboro, NC
... My back- ground in medical administration has equipped me with a strong understanding of regu- latory compliance, including FDA regulations and CGMP guidelines. I excel in analyzing data to identify quality improvements and am adept at collaborating ...
- Apr 18
High Point, NC
... 336-***-**** ad40aw@r.postjobfree.com High Point, NC 27265 FDA and HIPAA compliance Insurance verification Pharmacy operations Drug inventory control Insurance billing Restock shelves Serve customers Label products Monitor pharmacy security Secure ...
- Apr 14
Kernersville, NC
... Rhode Island School of Electronics SMU Dartmouth- Nursing Massasoit Community College- Computer Programming Training Programs FDA CFR-21 ISO 9001 Customer Oriented Selling and Servicing Hematology application and instrumentation LIS/EHR integration ...
- Feb 15
High Point, NC
... the company gene therapy products through performing the following responsibilities: oActed as the global project manager for all clinical trials running in North America, Europe & Middle East, ensuring FDA inspection readiness status is maintained. ...
- Jan 01
Burlington, NC
... Organized and maintained FDA, IRB and GCP required regulatory documentation for individual sites and studies. Maintained ongoing study-specific clinical trial tracking documents and distributed as needed. Clinical Research Coordinator II Kelly ...
- 2023 Nov 25
Greensboro, NC
... While the company dealt with Food and Drug Administration (FDA) issues, tasked to manage client expectations. Senior Vice President of North American Pharmaceutical and Nutritional Product Sales (2003–2005) Guided North American nutritional and ...
- 2023 Nov 01
Kernersville, NC
... Made sure concourse was empty at end of the day to ensure safety to passengers Made sure FDA procedures were carried out. Worked directly with [departments, clients, management] to achieve safety. Mostly US AIR who was directly involved with the ...
- 2023 Sep 21