| Distance: | Resume alert | Resumes 111 - 120 of 25555 |
Quality Engineer Assurance
Atlanta, GA
... January 2010 to December 2013 Quality Engineer Bioform Medical January 2006 to December 2010 • Led quality improvements, risk assessments, supplier audits/capability studies, internal audits and quality assurance impact analyses for regulatory FDA ... - Aug 20
... January 2010 to December 2013 Quality Engineer Bioform Medical January 2006 to December 2010 • Led quality improvements, risk assessments, supplier audits/capability studies, internal audits and quality assurance impact analyses for regulatory FDA ... - Aug 20
Administrative Assistant Support Specialist
Mahwah, NJ
... • Ensured accuracy of change controls in batch records • Provided initial quality training for new Pharmaceutical Operators • Maintained records in compliance with departmental regulations, FDA, OSHA, and DEA • Calculated production product yields; ... - Aug 20
... • Ensured accuracy of change controls in batch records • Provided initial quality training for new Pharmaceutical Operators • Maintained records in compliance with departmental regulations, FDA, OSHA, and DEA • Calculated production product yields; ... - Aug 20
Clinical Research Project Management
Indianapolis, IN
... internal and external customers as a technical expert of the Reference Laboratory Interface Department Maintained accurate FDA compliant protocol specifications relating to medical data transfer, specification documentation, and format design and ... - Aug 20
... internal and external customers as a technical expert of the Reference Laboratory Interface Department Maintained accurate FDA compliant protocol specifications relating to medical data transfer, specification documentation, and format design and ... - Aug 20
Regulatory Compliance Director
Asbury Park, NJ
... DEA/FDA & state specific reporting (ARCOS/CSOS/WDD&3PL,NDC Database)/Microsoft Excel for Financial and Compliance analysis/Microsoft PowerPoint for Operational Management reviews, EDI/EPCIS 1.1,1.2/GS1 implementation point person for DSCSA ... - Aug 20
... DEA/FDA & state specific reporting (ARCOS/CSOS/WDD&3PL,NDC Database)/Microsoft Excel for Financial and Compliance analysis/Microsoft PowerPoint for Operational Management reviews, EDI/EPCIS 1.1,1.2/GS1 implementation point person for DSCSA ... - Aug 20
Project Manager
Rockland County, NY
... Ensured FDA warehouse compliance and ran audits. Handled supplier negotiations, procurement, and inventory using Lean Six Sigma practices. - Aug 19
... Ensured FDA warehouse compliance and ran audits. Handled supplier negotiations, procurement, and inventory using Lean Six Sigma practices. - Aug 19
Project Manager Program
Downingtown, PA
... Class II and III medical devices are categories defined by the FDA based on their level of risk to patients and the required regulatory controls for their approval. Experience with Class I, II Devices: Regulatory Pathways: Manufacturers often find ... - Aug 19
... Class II and III medical devices are categories defined by the FDA based on their level of risk to patients and the required regulatory controls for their approval. Experience with Class I, II Devices: Regulatory Pathways: Manufacturers often find ... - Aug 19
Drug Discovery Patient Care
Yucaipa, CA
... Regulatory Affairs: Familiarity with FDA regulations, ICH guidelines, and drug approval processes. Bioinformatics: Familiar with tools for sequence analysis, protein structure prediction, and molecular modeling (e.g., Gold, Hermes, PyRx, Biovia ... - Aug 19
... Regulatory Affairs: Familiarity with FDA regulations, ICH guidelines, and drug approval processes. Bioinformatics: Familiar with tools for sequence analysis, protein structure prediction, and molecular modeling (e.g., Gold, Hermes, PyRx, Biovia ... - Aug 19
Quality Assurance Engineer
Cypress, CA
... Conduct and maintain complete complaint files and databases for all customer complaints per US engineering activities in compliance with FDA Regulations, ISO 13485 and other national and international quality and regulatory (as applicable) ... - Aug 19
... Conduct and maintain complete complaint files and databases for all customer complaints per US engineering activities in compliance with FDA Regulations, ISO 13485 and other national and international quality and regulatory (as applicable) ... - Aug 19
Business Process Development
Austin, TX
... Clearance Held: Tier 2 Public Trust - Veterans Affairs, Dept Health and Human Services, CDC, FDA NIH, ITII. DoD Secret, TS SBI DoD Army BEN PILEWSKI Austin, TX 78750 703-***-**** ***.********@*****.***, Linkedin.com/in/benpilewski Hello, As the Sr ... - Aug 19
... Clearance Held: Tier 2 Public Trust - Veterans Affairs, Dept Health and Human Services, CDC, FDA NIH, ITII. DoD Secret, TS SBI DoD Army BEN PILEWSKI Austin, TX 78750 703-***-**** ***.********@*****.***, Linkedin.com/in/benpilewski Hello, As the Sr ... - Aug 19
Regulatory Affairs Quality Assurance
Boston, MA
... Regulatory Affairs June 2024 - Present Relevant Coursework: Regulatory Strategy for Product Development & Lifecycle Management, FDA Medical Device Regulation, Quality Management, Risk Management, Medical Device Development, Safety Sciences, Project ... - Aug 19
... Regulatory Affairs June 2024 - Present Relevant Coursework: Regulatory Strategy for Product Development & Lifecycle Management, FDA Medical Device Regulation, Quality Management, Risk Management, Medical Device Development, Safety Sciences, Project ... - Aug 19