- Actalent (Maple Grove, MN)
- …Communicate deliverable status cross-functionally to facilitate the product development process . - Serve as technical lead for given projects/products, identifying, ... advance R&D department technical ability and core competencies. Skills Medical device , New product development, Iso 13485, R&d, Solidworks, R&d engineering, Product… more
- Medtronic (Minneapolis, MN)
- …skills that will be used to work with various cross-functional teams while engaging senior -leader (Dir, Sr Dir, VP) stakeholders. We value what makes you unique. ... Clinical and Regulatory Solutions (MCRS) business is looking for a motivated Senior Program Manager with strong Lean Six Sigma expertise (Black Belt preferred)… more
- Fujifilm (St. Paul, MN)
- …with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other ... that requires assistance and/or reasonable accommodation with the job application process , please contact the Human Resources department via e-mail at_… more
- Medtronic (Brooklyn Center, MN)
- …individual to join our Medtronic Energy and Component Center (MECC) OpEx team as a Sr . Business Process PMO Manager. In this role, you will strategically lead a ... leverage the PMO governance to ensure alignment. As a ** Sr . Business Process PMO Manager,** you will:...Experience in project/program management in medical industry and/or medical device industry + PMP, PgPM, PfPM, Lean Six Sigma… more
- Olympus Corporation of the Americas (Brooklyn Park, MN)
- …NOTE: The role of Staff Engineers within Olympus's career ladder is between Sr . Engineer and Principal Eng. **Job Duties** + Provides technical leadership ... Life at Olympus (https://www.olympusamerica.com/careers) . **Job Description** The Staff R&D Engineer is responsible for all aspects of product development acting as… more
- Medtronic (Minneapolis, MN)
- …in a more connected, compassionate world. **A Day in the Life** The Sr . Clinical Director for Neuromodulation, Pain Therapies reports to the VP, Clinical Research ... generate clinical evidence in support of the business. The Sr . Clinical Director is responsible for supporting the clinical...as it applies to product lifecycle + Leads the process to define the key stakeholder needs (including but… more
- Actalent (Big Lake, MN)
- …regulations and ISO 13485 & FDA standards in link with the Manufacturing Quality Engineer activities. The Manufacturing QE acts as an Operational Lead for the QAR ... (Lead) - Transfer knowledge experience from the AO Quality Engineer when a project is mature enough to be...Compile and analyze statistical data in order to assess process capabilities and control processes and conduct Process… more
- Medtronic (Minneapolis, MN)
- …more connected, compassionate world. **A Day in the Life** The ** Senior ** **Regulatory Affairs Specialist** is responsible for developing regulatory strategies, ... submissions and obtaining and maintaining approval for products. Additionally, the Senior Regulatory Affairs Specialist is responsible for assessment of device… more
- ManpowerGroup (Becker, MN)
- Manpower Engineering is partnering with a leader in the Medical Device industry for a Quality Engineer . **Job Title: Quality Engineer ** **Location: Big Lake, ... & FDA standards in link with the Manufacturing Quality Engineer activities. The Manufacturing QE acts as an Operational...Compile and analyze statistical data in order to assess process capabilities and control processes and conduct Process… more
- Medtronic (Mounds View, MN)
- …Haven, Connecticut * Jacksonville, Florida The Global Functions IT team is seeking a Senior Principal IT Technical Analyst specializing in the Order to Cash (OTC) ... process . In this role, you will employ your deep...and Product Costing within the Life Sciences or Medical Device industry. You will showcase your strong background in… more