| Resume alert | Resumes 21 - 30 of 45 |
regulatory affairs
Lehighton, PA, 18235
... BRAUN MEDICAL INC., Allentown, PA 2006-2013 Medical Device/Pharmaceutical Company Regulatory Affairs Managed and directed all ADEs (Adverse Drug Events) to FDA, both current ADEs and literature searches. Researched the package insert of the drug and ... - 2015 Jun 23
... BRAUN MEDICAL INC., Allentown, PA 2006-2013 Medical Device/Pharmaceutical Company Regulatory Affairs Managed and directed all ADEs (Adverse Drug Events) to FDA, both current ADEs and literature searches. Researched the package insert of the drug and ... - 2015 Jun 23
Accounting Human Resources
Duryea, PA
... •Full P&L Statements •Employee benefit program, Medical, Life, etc •Controlled Substance Reporting (FDA) (Narcotics) •Data Processing department reported to me. Company went out of business in March 1995 EDUCATION Attended Penn State-Altoona Campus, ... - 2015 Jun 17
... •Full P&L Statements •Employee benefit program, Medical, Life, etc •Controlled Substance Reporting (FDA) (Narcotics) •Data Processing department reported to me. Company went out of business in March 1995 EDUCATION Attended Penn State-Altoona Campus, ... - 2015 Jun 17
Sales Leadership, Marketing Leadership, Customer/Trade Marketing Leade
Mountain Top, PA
... Traveled internationally to negotiate long term contracts with over 15 new manufacturing partners (China, Singapore, Malaysia, Germany) to lead product development, FDA compliance, and supply chain deliverables . Developed equipment maintenance ... - 2015 May 06
... Traveled internationally to negotiate long term contracts with over 15 new manufacturing partners (China, Singapore, Malaysia, Germany) to lead product development, FDA compliance, and supply chain deliverables . Developed equipment maintenance ... - 2015 May 06
Management Sales
Tobyhanna, PA, 18466
... The project goal was to implement an Argus environment integrated with a FDA and EMEA for compliance and regulatory needs and generated intelligence reports on clinical trial and data collected for adverse effect. Responsibilities: Evaluated the ... - 2015 Feb 10
... The project goal was to implement an Argus environment integrated with a FDA and EMEA for compliance and regulatory needs and generated intelligence reports on clinical trial and data collected for adverse effect. Responsibilities: Evaluated the ... - 2015 Feb 10
Sales Account Executive
Stroudsburg, PA
... Marketing – Successful at marketing complex scientific and engineering concepts to government agencies (FDA and the Office of Science Technology Policy at the White House), hospitals, and professional healthcare and engineering associations. ... - 2015 Jan 16
... Marketing – Successful at marketing complex scientific and engineering concepts to government agencies (FDA and the Office of Science Technology Policy at the White House), hospitals, and professional healthcare and engineering associations. ... - 2015 Jan 16
Quality Assurance
Wilkes-Barre, PA
... TEVA PHARMACEUTICALS., Fairfield, NJ / Sellersville, PA 2006 - 2009 Assistant Engineer / Associate Engineer Generate process characterization/technical protocols, reports, stability summaries and FDA summaries based upon process characterization ... - 2014 Aug 17
... TEVA PHARMACEUTICALS., Fairfield, NJ / Sellersville, PA 2006 - 2009 Assistant Engineer / Associate Engineer Generate process characterization/technical protocols, reports, stability summaries and FDA summaries based upon process characterization ... - 2014 Aug 17
Technician Safety
Bartonsville, PA, 18321
... regarding safety issues that were observed during inspections and testing • Maintain qualifications for working in FDA controlled production buildings and access to TSA shipping areas Emergency Medical Technician Northern Valley EMS 7/2008 ... - 2014 Jul 10
... regarding safety issues that were observed during inspections and testing • Maintain qualifications for working in FDA controlled production buildings and access to TSA shipping areas Emergency Medical Technician Northern Valley EMS 7/2008 ... - 2014 Jul 10
BioPharma Technical Writer /QC Associate
Stroudsburg, PA
... Project Change Control documentation DCO tracking, cGMP practices, Research and Development, FDA Part 11, 210 &211 and 820 requirements for GMP's, GDP's, Document Management, Protocol Specification modification processing. Performs red- line editing ... - 2014 Mar 13
... Project Change Control documentation DCO tracking, cGMP practices, Research and Development, FDA Part 11, 210 &211 and 820 requirements for GMP's, GDP's, Document Management, Protocol Specification modification processing. Performs red- line editing ... - 2014 Mar 13
Customer Service Project Manager
Drums, PA, 18222
... as Chair of Relay for Life in 2012 Recognized for, “Mammography Excellence”, by Community Health Systems, after passing ACR/FDA compliance Operations Manager Advanced Radiology Services • East Stroudsburg, PA 2004-2010 Radiology Supervisor Advanced ... - 2013 Dec 11
... as Chair of Relay for Life in 2012 Recognized for, “Mammography Excellence”, by Community Health Systems, after passing ACR/FDA compliance Operations Manager Advanced Radiology Services • East Stroudsburg, PA 2004-2010 Radiology Supervisor Advanced ... - 2013 Dec 11
Customer Service Supply Chain
Kingston, PA
... Project/Program Management Process Innovation/Improvement KPIs/Fulfillment/e-Commerce Cost Productivity/Containment DOT/USDA/FDA/DEP/OSHA/HAZMAT Compliance High-Volume SKU Management Materials Planning/Purchasing Facility/Product/Service Start-Up ... - 2013 Jul 28
... Project/Program Management Process Innovation/Improvement KPIs/Fulfillment/e-Commerce Cost Productivity/Containment DOT/USDA/FDA/DEP/OSHA/HAZMAT Compliance High-Volume SKU Management Materials Planning/Purchasing Facility/Product/Service Start-Up ... - 2013 Jul 28