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FDA resumes in Saint Paul, MN

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Resume alert Resumes 61 - 70 of 285

Network Engineer Manager

Saint Paul, MN
... Planned and brought in house a previously outsourced FDA medical device clinical trial utilizing Clindex, Sybase, Oracle and virtual Citrix servers saving the company more than $800,000. Virtualized and upgraded multiple legacy servers to Windows ... - 2020 Nov 03

Quality Engineer Manager

Minneapolis, MN
... Creation, implementation, and execution of process that ensures direct import food use products are properly classified per FDA and US Customs requirements. Helped develop and implement process to ensure California Proposition 65 requirements are ... - 2020 Nov 03

Manager Quality

Minneapolis, MN
... and hire personnel and create opportunities for growth with existing and new customers AREAS OF EXPERTISE Quality Assurance FDA Regulations Leadership/Training ISO Certification 9001 Prop 65 chemicals Process Validation Contract Manufacturing Vendor ... - 2020 Oct 21

Manager Scrum

Prior Lake, MN
... Paul Area Lead high profile Imaging - patient related ERP, Web, SaaS (Google Apps, Dropbox, Salesforce, Cisco WebEx, Concur, GoToMeeting), HR (Success Factors), Cloud Based, and Data Warehouse projects which had to meet FDA, MDH, HIPPA, and various ... - 2020 Oct 04

Engineering Medical Device

Minneapolis, MN
... MyBioGate Inc, Houston, Texas July 2018- Dec 2018 Medical Device Analyst Intern Built a database through researching over 200 FDA approved medical products daily using Excel Evaluated medical device companies based on patent landscape, market ... - 2020 Sep 18

Senior Manager, Packaging Innovation and Commercialization

Minneapolis, MN
... SKILLS Packaging development & commercialization Lean Six Sigma manufacturing Cost & waste reduction & continuous improvement Strategy & execution FDA & EPA regulatory compliance Risk mitigation Project management Product development Quality control ... - 2020 Jul 07

Clinical Research Medical

Minneapolis, MN
... Knowledge of FDA regulations and IRB requirements: 21 CFR, EU MDD, ISO 13485, and 14155, GCP and ICH Standards for medical devices. Knowledge of Clinical Product Life Cycle. Knowledge of Quality fundamentals, Lean Six Sigma and CAPA. Failure Mode ... - 2020 Jun 30

Design Engineer Electrical

Minneapolis, MN
... Well-versed in the formal and informal testing of FDA and FCC-certified devices. Also experienced in prototyping efforts, requirements generation and problem analysis/resolution for complex electronic devices. Contributions designing and testing ... - 2020 Jun 27

Clinical Research Assistant

Hudson, WI
... Basic Understanding of FDA Regulations. High attention to detail and accuracy. Demonstrated communication skills, both written and verbal. Experience working with clinical trial management systems and clinical document control systems/eTMF WORK ... - 2020 Jun 19

Quality Engineer

Eagan, MN
... SKILLS Knowledge of FDA and ISO regulations Proven Project Management skills Excellent Verbal and Written Communication Skills Ability to work independently or in Team Supplier Corrective Action Requests (SCAR) Excellent Leadership skills Experience ... - 2020 May 19
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