| Resume alert | Resumes 71 - 80 of 179 |
Materials
St. Petersburg, FL
... 02/18 – Current – QC Inspector Inspect/Test Vendor Manufactured TIPS before receiving into stock per assigned Company Quality Standards, FDA 21 CFR820, ISO 13485:2003 AND cGMP. Complete Inspection documentation. Verify final assembly of manufactured ... - 2018 Dec 27
... 02/18 – Current – QC Inspector Inspect/Test Vendor Manufactured TIPS before receiving into stock per assigned Company Quality Standards, FDA 21 CFR820, ISO 13485:2003 AND cGMP. Complete Inspection documentation. Verify final assembly of manufactured ... - 2018 Dec 27
Drug Regulatory affairs, medical devices
Tampa, FL
... Data Management, Coral draw, Adobe • Diligence and tendency towards pursuit of a problem till end • recognize roles of FDA and other standard setting organizations, their perspective on drug quality and the tools they use to ensure standards. ... - 2018 Dec 10
... Data Management, Coral draw, Adobe • Diligence and tendency towards pursuit of a problem till end • recognize roles of FDA and other standard setting organizations, their perspective on drug quality and the tools they use to ensure standards. ... - 2018 Dec 10
Project Manager Quality
Largo, FL, 33778
... Subject matter expert in ISO 9001 and FDA compliance with proven strengths in driving achievement of corporate quality objectives. Known for achievements in earning high customer satisfaction ratings while increasing productivity. Trained in Gallup ... - 2018 Dec 06
... Subject matter expert in ISO 9001 and FDA compliance with proven strengths in driving achievement of corporate quality objectives. Known for achievements in earning high customer satisfaction ratings while increasing productivity. Trained in Gallup ... - 2018 Dec 06
Medical Health
Tampa, FL
... Ensured compliance of Food and Drug Administration (FDA) Code of Federal Regulations, good Page 3 of 4 laboratory practices and good clinical practices of medical devices. Established research and development protocols for the performance of ... - 2018 Oct 19
... Ensured compliance of Food and Drug Administration (FDA) Code of Federal Regulations, good Page 3 of 4 laboratory practices and good clinical practices of medical devices. Established research and development protocols for the performance of ... - 2018 Oct 19
Junior Business Analyst
Clearwater, FL
... for requests that meet FDA indicated diagnoses and CMS guidelines ●Escalate denials and requests requiring extensive clinical review to pharmacists ●Develop reports and provided them to providers, and/or management Data Entry Technician Dec. ... - 2018 Oct 08
... for requests that meet FDA indicated diagnoses and CMS guidelines ●Escalate denials and requests requiring extensive clinical review to pharmacists ●Develop reports and provided them to providers, and/or management Data Entry Technician Dec. ... - 2018 Oct 08
Technical Writer/Editor
Clearwater, FL
... 8/2014-1/2015, (Contract) Technical Editor/Writer, Actavis Laboratories FL, Inc., Davie, FL In support of Pharmaceutical Technologies, ensured compliance with the FDA current Good Documentation/Manufacturing Practices (cGD/MPs). Updated Bottle ... - 2018 Oct 01
... 8/2014-1/2015, (Contract) Technical Editor/Writer, Actavis Laboratories FL, Inc., Davie, FL In support of Pharmaceutical Technologies, ensured compliance with the FDA current Good Documentation/Manufacturing Practices (cGD/MPs). Updated Bottle ... - 2018 Oct 01
ServiceNow Consultant
Tampa, FL
... System (CCMS) TrackWise • Performed IQ and OQ for validated systems like LIMS following SOP and GDP • Experienced working in GMP/FDA regulated environment • Supported applications hosted on Citrix • Experienced working with highly technical end user ... - 2018 Sep 29
... System (CCMS) TrackWise • Performed IQ and OQ for validated systems like LIMS following SOP and GDP • Experienced working in GMP/FDA regulated environment • Supported applications hosted on Citrix • Experienced working with highly technical end user ... - 2018 Sep 29
Quality Assurance Philosophies, Techniques
Palm Harbor, FL
... Develop train and manage audit teams to ensure FDA, GMPs and ISO compliance. Assemble and lead process improvement teams to resolve issues, improve/optimize existing functions. Spearhead and develop cost saving initiatives /projects. Lead and ... - 2018 Sep 14
... Develop train and manage audit teams to ensure FDA, GMPs and ISO compliance. Assemble and lead process improvement teams to resolve issues, improve/optimize existing functions. Spearhead and develop cost saving initiatives /projects. Lead and ... - 2018 Sep 14
Medical Device Quality
Safety Harbor, FL, 34695
... SUMMARY OF QUALIFICATIONS: Auditing, FDA, FAA, QMS, QSR, ISO, AS, Regulatory Affairs, Complaint Investigation, CAPA, Documentation, Statistical Process Control, Equipment Calibration, Inspection, G, D & T, Supplier Surveillance (SQE), Lean ... - 2018 Aug 27
... SUMMARY OF QUALIFICATIONS: Auditing, FDA, FAA, QMS, QSR, ISO, AS, Regulatory Affairs, Complaint Investigation, CAPA, Documentation, Statistical Process Control, Equipment Calibration, Inspection, G, D & T, Supplier Surveillance (SQE), Lean ... - 2018 Aug 27
Quality Engineer Manager
Apollo Beach, FL, 33572
... Drove all drug regulatory knowledge and strategy to the organization ensuring understanding and adherence to target region PET drug regulations and licensing requirements - emphasis on US FDA, EU and US Pharmacopoeia, ANDA and GMP requirements. ... - 2018 Aug 26
... Drove all drug regulatory knowledge and strategy to the organization ensuring understanding and adherence to target region PET drug regulations and licensing requirements - emphasis on US FDA, EU and US Pharmacopoeia, ANDA and GMP requirements. ... - 2018 Aug 26