| Job alert | Jobs 1 - 10 of 288 |
Software Verification Engineer
Blue Star Partners LLC
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Saint Paul, MN
... Role, Responsibilities, and Deliverables: Work independently and as a team member to plan, write, and execute test cases according to company practices, FDA regulatory, and ISO standard procedures. Design new test suites for new features and ... - Apr 06
Toolroom Supervisor
Cretex
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Coon Rapids, MN, 55433
... technical degree Supervisory experience Medical manufacturing experience Familiar with ISO and FDA requirements Certifications in a related field rms Company Benefits As a Cretex Medical company, rms offers a full benefit package to its employees. ... - May 03
Sr Manufacturing Engineer
VitalPath
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North Saint Paul, MN, 55109
... You will be responsible for the support and troubleshooting of the entire scope of the manufacturing process and direct participation in managing CIs, quality issues investigations NMRs to ensure full compliance to FDA QSR and applicable ISO 13485 ... - May 03
Regulatory Affairs Manager
Custom Search, Inc.
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Minnetonka, MN, 55345
... Support inspections by FDA, notified body, and other regulatory agencies. Desired Profile: Bachelor’s Degree with at least 5-8 years of related Regulatory experience, mostly in medical devices. 1+ years’ experience in a Regulatory Affairs management ... - Apr 26
Electrical Engineer (medical device)
Intellectt INC
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Saint Paul, MN
... Demonstrates commitment to the development, implementation and effectiveness of Abbott Quality Management System per ISO, FDA, and other regulatory agencies. Top 3 skills manager is looking for: Electrical engineering in medical device space, ... - May 01
Quality Engineer
TALENT Software Services
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Saint Paul, MN, 55130
... Providing continuous and rigorous assessment of Material control processes to ensure compliance with FDA regulations, ISO 13485, and Medical Device Requirements and applicable global regulations. Ownership of highly visible, global, systemic CAPAs. ... - May 03
Assembler
CathX
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Fort Snelling, MN, 55111
... This role complies to FDA QSR (21 CFR 820), ISO 13485 requirements and adheres to the Quality Management System (QMS). ESSENTIAL FUNCTIONS: Reads work orders, follows production drawings and sample assemblies, or receives verbal instructions ... - Apr 12
RN - Medical Policy/Utilization Management
Javen Technologies
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Eagan, MN, 55122
... Research issues on an ad hoc basis to determine coverage status of other health plans, FDA approval status; this may also require limited research of evidence-based literature. Lead work groups as needed. Lead projects that support Medical Policy ... - Apr 20
Manufacturing / Process Development Engineer
Hemostasis, LLC
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White Bear Lake, MN
... specific technical support as needed · Lead projects or project teams, as needed · Understand and comply with ISO 13485, FDA, and CE requirements · Generate and maintain all aspects of design history records per the Hemostasis Quality Management ... - Apr 15
Sanitation Supervisor
Great Lakes Coca-Cola
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Saint Paul, MN
... Position Responsibilities may include, but not limited to: Assist with completion of and ensure compliance with Good Manufacturing Practices (GMP), Process, ISO, Kore, FDA, etc., audits Ensure plant meets or exceeds all GMP requirements Collaborate ... - Apr 24