| Resume alert | Resumes 11 - 20 of 285 |
Technical Publications Project Manager
Minneapolis, MN, 55488
... • Editing and preparing for publication, internal documents for FDA approval, such as the Device Labeling document. • Complying with the General Provisions of FDA CFR, Parts 11, 810, 812, and 820. • Designing and implementing context-sensitive on ... - Feb 21
... • Editing and preparing for publication, internal documents for FDA approval, such as the Device Labeling document. • Complying with the General Provisions of FDA CFR, Parts 11, 810, 812, and 820. • Designing and implementing context-sensitive on ... - Feb 21
Machine Operator Customer Service
Saint Paul, MN
... quality control to ensure that products met or exceeded expectations • Worked according to guidelines set by OSHA and the FDA to ensure safety of product Temporary Associate 2/14 – 12/14 Manpower (at Con Agra) • Met or exceeded production goals ... - Feb 19
... quality control to ensure that products met or exceeded expectations • Worked according to guidelines set by OSHA and the FDA to ensure safety of product Temporary Associate 2/14 – 12/14 Manpower (at Con Agra) • Met or exceeded production goals ... - Feb 19
Maintenance/forklift
Minneapolis, MN
... Local and international ●Proficient with ISO/FDA documentation ●Service Tech for injection mold and production ●Got proficient with Castillo software Training/Certificates ●Hazardous Waste Training ●Forklift Training STARKEY JOB SUMMARY While ... - Feb 19
... Local and international ●Proficient with ISO/FDA documentation ●Service Tech for injection mold and production ●Got proficient with Castillo software Training/Certificates ●Hazardous Waste Training ●Forklift Training STARKEY JOB SUMMARY While ... - Feb 19
Data Scientist Analytics
Minneapolis, MN
... Led two retrospective cardiovascular medical device studies requested by FDA, determined study limitations by literature review for sample size, power, methods, table shells, and novel approach. Determined sample sizes for new studies and ... - Feb 18
... Led two retrospective cardiovascular medical device studies requested by FDA, determined study limitations by literature review for sample size, power, methods, table shells, and novel approach. Determined sample sizes for new studies and ... - Feb 18
Clinical Research Nurse
Saint Paul, MN
... (Duopa had been with Abbott and Solvay Pharmaceuticals and was FDA approved in May 2015.) • Interacted directly with neurologists and clinic staff on proper use of the medication and pump/device. Advised Endoscopy and Surgical OR staff on surgical ... - Feb 10
... (Duopa had been with Abbott and Solvay Pharmaceuticals and was FDA approved in May 2015.) • Interacted directly with neurologists and clinic staff on proper use of the medication and pump/device. Advised Endoscopy and Surgical OR staff on surgical ... - Feb 10
Regulatory Affairs Technical Documentation
Anoka, MN
... Equipped with a strong scientific and technical background and well-versed in U.S FDA Regulation, EU MDD and MDR 2017/745, and other international medical device, drugs, and biologics regulations. Effective leader, accustomed to building, mentoring, ... - Feb 09
... Equipped with a strong scientific and technical background and well-versed in U.S FDA Regulation, EU MDD and MDR 2017/745, and other international medical device, drugs, and biologics regulations. Effective leader, accustomed to building, mentoring, ... - Feb 09
Quality Control Assurance Specialist
Andover, MN
... •Knowledge ISO13485/ISO 9001 Standards •Knowledge of FDA regulations & requirement in Medical industry. •Tooling •Detail oriented •Environmental monitoring. •Able to recognize major and minor defects in product workmanship. •Ability to work ... - Jan 28
... •Knowledge ISO13485/ISO 9001 Standards •Knowledge of FDA regulations & requirement in Medical industry. •Tooling •Detail oriented •Environmental monitoring. •Able to recognize major and minor defects in product workmanship. •Ability to work ... - Jan 28
Quality Control Maintenance Worker
Blaine, MN
... Amport Foods,Minneapolis MN — Quality Control Technician February 1998-March 2016 Enforcing the company policy toward producing good products in all production processes developed,following the standards established by the FDA and OSHA as are GMP ... - Jan 27
... Amport Foods,Minneapolis MN — Quality Control Technician February 1998-March 2016 Enforcing the company policy toward producing good products in all production processes developed,following the standards established by the FDA and OSHA as are GMP ... - Jan 27
Clinical Research Project Management
Plymouth, MN
... Proficient in research protocols, FDA regulations, and clinical trial operations. Skilled in project management, clinical trial software, and data management. Detail-oriented problem solver with a keen interest in enhancing healthcare systems. Quick ... - Jan 23
... Proficient in research protocols, FDA regulations, and clinical trial operations. Skilled in project management, clinical trial software, and data management. Detail-oriented problem solver with a keen interest in enhancing healthcare systems. Quick ... - Jan 23
Six Sigma Process Improvement
Maple Grove, MN
... Technical support of manufacturing operations, equipment and processes validation (IQ, OQ and PQ) Attention to details and adhering to FDA standards and quality initiatives. Tested protocols using Minitab - SPC statistical analysis software ... - 2023 Dec 16
... Technical support of manufacturing operations, equipment and processes validation (IQ, OQ and PQ) Attention to details and adhering to FDA standards and quality initiatives. Tested protocols using Minitab - SPC statistical analysis software ... - 2023 Dec 16