ValleyfairApple Valley
Keep guests safe at our Water Park and earn a PAID lifeguard certification to administer CPR and First Aid!.Maintain vigilance of the water park, pools, slides and lazy river.Test equipment before opening attractions to guests.Maintain "Test Ready" at all times.Properly use and store rescue equipmen...
Diverse LynxMinneapolis, 10 mi from Plymouth (MN)
Job Title: Data Scientist with NLP exp
Job Location Minneapolis MN
Job Location: Fulltime permanent only
Requirements:
Develop and implement data-driven solutions that drive business value and support the company's strategic goals.
Collaborate...
Axelon Services CorporationPlymouth (MN)
applicants without medical, scientific, or complaint handling experience may be considered if they possess the strengths suitable for this position.
Duties:
May perform multiple functions within the postmarket surveillance department.
Major...
ICONMA, LLCPlymouth (MN)
Four-year degree, preferably in the healthcare or science fields; or 2-year degree and relevant experience supporting complaint handling investigations, medical device reporting, or product analysis.
Degreed applicants without medical, scientific...
ProtingentOakdale (MN), 24 mi from Plymouth (MN)
Job Description
Position Title: Laboratory Engineer/Scientist
Position Description: Protingent Staffing has an exciting direct hire opportunity for Laboratory Engineer/Scientist with our client located in Oakdale, MN.
Job Responsibilities...
Harbor Freight ToolsMinneapolis, 10 mi from Plymouth (MN)
create strategic roadmaps, and successfully lead, grow, and hire a team of ML Engineers.
Duties and Responsibilities
• Work closely with data scientists and IT in the design, development, and implementation of our Enterprise AI platform.
• Design, build...
Abbott LaboratoriesMaple Grove (MN), 4 mi from Plymouth (MN)
and scientists.
For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring system, innovative therapies for treating heart disease, or products that help people...
TargetBrooklyn Park (MN), 5 mi from Plymouth (MN)
vacation. Find competitive benefits from financial and education to well-being and beyond at https://corporate.target.com/careers/benefits.
JOIN TARGET AS A SENIOR DATA SCIENTIST – DEMAND FORECASTING
About us:
Working at Target means helping all families...
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Analyst, Safety Regulatory Reporting and Global Compliants
Plymouth (MN) | www.resume-library.com |
Title : Analyst, Safety Regulatory Reporting and Global Complaints
Location : 6000 Nathan Lane N, Plymouth, MN 55442 United States
Duration : 6 Months contract
Job description:
Qualifications:
Must be at least 18 years of age.
High School Diploma required.
Bachelors Degree in Engineering, Medical Sciences, or other related scientific field required.
2+ years experience in a health care environment, and/or within a quality/compliance/regulatory organization in an FDA regulated business preferred.
US FDA Medical Device Reporting and experience with Trackwise Digital preferred.
Position Summary
The temporary position is responsible for managing device complaints and adverse events globally. This may include: complaint initial triage, submitting regulatory reports in accordance with applicable regulations, referring potential safety cases to applicable department, providing updates to reports, reviewing for closure/reopening as needed, and assuring timely processing of complaints.
Essential Duties & Responsibilities
Responsible for evaluating complaints from patient safety perspective and completing regulatory reporting decisions per reporting requirements globally.
Responsible for creating and submitting regulatory reports to the FDA.
Works independently and is accountable for completing task as assigned.
Works well in a team to accomplish team goals.
Knowledge & Skills
Experience with or knowledge of medical terminology and how medical/pharmaceutical products are typically used in a clinical setting.
Basic computer and software skills.
Must be able to communicate effectively with internal and external customers.
Demonstrate ability to collect, analyze and interpret complaint and adverse event information.
Location : 6000 Nathan Lane N, Plymouth, MN 55442 United States
Duration : 6 Months contract
Job description:
Qualifications:
Must be at least 18 years of age.
High School Diploma required.
Bachelors Degree in Engineering, Medical Sciences, or other related scientific field required.
2+ years experience in a health care environment, and/or within a quality/compliance/regulatory organization in an FDA regulated business preferred.
US FDA Medical Device Reporting and experience with Trackwise Digital preferred.
Position Summary
The temporary position is responsible for managing device complaints and adverse events globally. This may include: complaint initial triage, submitting regulatory reports in accordance with applicable regulations, referring potential safety cases to applicable department, providing updates to reports, reviewing for closure/reopening as needed, and assuring timely processing of complaints.
Essential Duties & Responsibilities
Responsible for evaluating complaints from patient safety perspective and completing regulatory reporting decisions per reporting requirements globally.
Responsible for creating and submitting regulatory reports to the FDA.
Works independently and is accountable for completing task as assigned.
Works well in a team to accomplish team goals.
Knowledge & Skills
Experience with or knowledge of medical terminology and how medical/pharmaceutical products are typically used in a clinical setting.
Basic computer and software skills.
Must be able to communicate effectively with internal and external customers.
Demonstrate ability to collect, analyze and interpret complaint and adverse event information.
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