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Resume alert |
Resumes 11 - 20 of 296 |
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
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
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
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
Rogers, MN
... Provided support for FDA submissions. Business unit VP liaison with 45 software and hardware engineers. Contractor, Environmental, Health and Safety, Corporate Services Identified ISO 9001 auditors and initiated Scope of Work and Request for ...
- Feb 18
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
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
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
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
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