| Distance: | Resume alert | Resumes 381 - 390 of 25500 |
Trade Compliance Leader with 25+ Years Experience
El Paso, TX
... Deep expertise in CBP/CBSA regulations, HTSUS/HS classification, valuation, country of origin, and FDA- regulated imports for medical devices and safety equipment. Builds audit-ready programs—SOPs, internal controls, broker governance, and CF28/CF29 ... - Jan 21
... Deep expertise in CBP/CBSA regulations, HTSUS/HS classification, valuation, country of origin, and FDA- regulated imports for medical devices and safety equipment. Builds audit-ready programs—SOPs, internal controls, broker governance, and CF28/CF29 ... - Jan 21
Senior Quality Engineer Med Device & Manufacturing
Ocala, FL
... Experience/Skills include: ISO 9001 & 13485 Quality Engineering/Systems/Management Six Sigma principles Lean Manufacturing FDA/cGMP regulations Supplier Management Design Controls ISO 14001 Management Review Internal/External Audits MS Office – Word ... - Jan 21
... Experience/Skills include: ISO 9001 & 13485 Quality Engineering/Systems/Management Six Sigma principles Lean Manufacturing FDA/cGMP regulations Supplier Management Design Controls ISO 14001 Management Review Internal/External Audits MS Office – Word ... - Jan 21
Biomedical Engineer - Clinical Research & Tissue Recovery Specialist
Salt Lake City, UT
... , Undergraduate Research Scholar Distinction EXPERIENCE Ocular Tissue Recovery Specialist III Aug 2022 – Present Utah Lions Eye Bank, Murray, UT • Performed 400+ aseptic corneal and ocular tissue recoveries under FDA and EBAA regulatory standards. ... - Jan 21
... , Undergraduate Research Scholar Distinction EXPERIENCE Ocular Tissue Recovery Specialist III Aug 2022 – Present Utah Lions Eye Bank, Murray, UT • Performed 400+ aseptic corneal and ocular tissue recoveries under FDA and EBAA regulatory standards. ... - Jan 21
Senior Technical Program Manager - Retail IT Solutions
San Jose, CA
... ● Integrated business applications and created required reports from EZCap application for audit and FDA and ICD code requirements. ● Led a integration pilot with Epic to EZCap. ● Developing and sharing required reports for executives on regular ... - Jan 20
... ● Integrated business applications and created required reports from EZCap application for audit and FDA and ICD code requirements. ● Led a integration pilot with Epic to EZCap. ● Developing and sharing required reports for executives on regular ... - Jan 20
Matchmaking & Sales Professional - Client Relationships Expert
Lebanon, NJ
... • Social Media Advertising consultant Massage Envy Customer Service and Office Manager/Sales 2018 • Customer Service/FDA/Wellness Advisor/Member Concierge • Answered basic customer emails and phone calls • Checking clients in and out • Booking ... - Jan 20
... • Social Media Advertising consultant Massage Envy Customer Service and Office Manager/Sales 2018 • Customer Service/FDA/Wellness Advisor/Member Concierge • Answered basic customer emails and phone calls • Checking clients in and out • Booking ... - Jan 20
Experienced CDL Driver & Property Manager, Ready for Relocation
Bridgeport, CT, 06610
... Partnered with NASA, Bemer is a FDA Class II Consumer Medical Device: BEMER (bio- electromagnetic energy regulation) for preventative health and wellness, discomforts, injury, or illness for horses and humans. Regional OTR Driver Schneider National ... - Jan 20
... Partnered with NASA, Bemer is a FDA Class II Consumer Medical Device: BEMER (bio- electromagnetic energy regulation) for preventative health and wellness, discomforts, injury, or illness for horses and humans. Regional OTR Driver Schneider National ... - Jan 20
IT Sales Professional with Medical Solutions Experience
Ashburn, VA
... Maintained accountability for all pharmaceutical samples and stock packages in accordance with FDA and PDMA. Planed, support, host attended various company functions, included events scheduled before or after regular working hours. Accomplishments: ... - Jan 19
... Maintained accountability for all pharmaceutical samples and stock packages in accordance with FDA and PDMA. Planed, support, host attended various company functions, included events scheduled before or after regular working hours. Accomplishments: ... - Jan 19
Regulatory Affairs Expert 25+ Years in Pharma Regulatory
Cape Coral, FL
... Owner, Data Verification, Proofreading, SharePoint, eCTD regulatory submissions management including advanced user status and FDA Gateway expertise, ANGEL, eCTDXPress, Lorenz Validator, Virtual Document creation/concatenation, stability auditing. ... - Jan 18
... Owner, Data Verification, Proofreading, SharePoint, eCTD regulatory submissions management including advanced user status and FDA Gateway expertise, ANGEL, eCTDXPress, Lorenz Validator, Virtual Document creation/concatenation, stability auditing. ... - Jan 18
Quality Assurance Leader Medical Devices & ISO Standards
Porter, TX
... 2/2022- 8/2023 Director of Quality - Houston, TX Responsible for assessing the current Quality Management System and implementing changes to assure compliance with FDA Part 820 Quality System Regulations, ISO-13485 and ISO-14971. Identified and ... - Jan 17
... 2/2022- 8/2023 Director of Quality - Houston, TX Responsible for assessing the current Quality Management System and implementing changes to assure compliance with FDA Part 820 Quality System Regulations, ISO-13485 and ISO-14971. Identified and ... - Jan 17
Pharmaceutical Compliance & Validation Specialist
Jopul, Maharashtra, India
... Reviewed and Validated Computer Systems in compliance with 21 CFR Part 11 and GxP FDA Regulations. Actively participated in the Validation Life Cycle of regulated projects by reviewing validation documentation, participating in application ... - Jan 17
... Reviewed and Validated Computer Systems in compliance with 21 CFR Part 11 and GxP FDA Regulations. Actively participated in the Validation Life Cycle of regulated projects by reviewing validation documentation, participating in application ... - Jan 17