• Snapboard
  • Activity
  • Reports
  • Campaign
Welcome ,

Chat with the recruiter

...Minimize

Hey I'm Online! Leave me a message.
Let me know if you have any questions.

Postmarket Surveillance Analyst

In Minnesota / United States

Save this job

Postmarket Surveillance Analyst   

Click on the below icons to share this job to Linkedin, Twitter!

JOB TITLE:

Postmarket Surveillance Analyst

JOB TYPE:

JOB SKILLS:

JOB LOCATION:

Plymouth Minnesota / United States

JOB DESCRIPTION:

Postmarket Surveillance Analyst
Pay Rate: $21.43/HR
8:00 AM- 5:00 PM

Cortech is seeking a Postmarket Analyst in Plymouth, MN.


Job Description:
o Review complaint communications and assess for regulatory compliance, reportability, and potential impact to patient safety and business operations.
o Apply clinical knowledge, as related to product application, to evaluate identified complaints.
o Investigate complaints by gathering sufficient data from clinical staff, field representatives, internal employees, and laboratory analysis.
o Establish regulatory reportability decisions using event investigation and regulatory decision models.
o Participate in development and modification of these decision models with changes in product advances/therapies to uphold consistent compliance with government-mandated regulations.
o Write Medical Device Reports (MDRs), MedWatch, Vigilance, and other regulatory reports, ensuring timely transmission to the appropriate regulatory authorities.
o Apply codes to events to facilitate product performance records.
o Review coding and investigations with engineering, laboratory, and other internal staff.
o Compose written communications detailing the clinical observation, investigation and/or product
analysis, and corrective actions, as applicable, to physician and other end use customers.
o Review complaint communications and assess for regulatory compliance, reportability, and potential
impact to patient safety and business operations.
o Apply clinical knowledge, as related to product application, to evaluate identified complaints.
o Investigate complaints by gathering sufficient data from clinical staff, field representatives, internal
employees, and laboratory analysis.
o Establish regulatory reportability decisions using event investigation and regulatory decision models.
o Participate in development and modification of these decision models with changes in product
advances/therapies to uphold consistent compliance with government-mandated regulations.
o Write Medical Device Reports (MDRs), MedWatch, Vigilance, and other regulatory reports, ensuring
timely transmission to the appropriate regulatory authorities.
o Apply codes to events to facilitate product performance records.
o Review coding and investigations with engineering, laboratory, and other internal staff.
o Compose written communications detailing the clinical observation, investigation and/or product
analysis, and corrective actions, as applicable, to physician and other end use customers.
o Communications include determination/eligibility for warranty credit or unreimbursed medical
payments

Position Details

POSTED:

Aug 07, 2021

EMPLOYMENT:

INDUSTRY:

SNAPRECRUIT ID:

S16204860905715742

LOCATION:

Minnesota / United States

CITY:

Plymouth

Job Origin:

Jobsrus_organic_feed

A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Postmarket Surveillance Analyst    Apply

Click on the below icons to share this job to Linkedin, Twitter!

Postmarket Surveillance Analyst
Pay Rate: $21.43/HR
8:00 AM- 5:00 PM

Cortech is seeking a Postmarket Analyst in Plymouth, MN.


Job Description:
o Review complaint communications and assess for regulatory compliance, reportability, and potential impact to patient safety and business operations.
o Apply clinical knowledge, as related to product application, to evaluate identified complaints.
o Investigate complaints by gathering sufficient data from clinical staff, field representatives, internal employees, and laboratory analysis.
o Establish regulatory reportability decisions using event investigation and regulatory decision models.
o Participate in development and modification of these decision models with changes in product advances/therapies to uphold consistent compliance with government-mandated regulations.
o Write Medical Device Reports (MDRs), MedWatch, Vigilance, and other regulatory reports, ensuring timely transmission to the appropriate regulatory authorities.
o Apply codes to events to facilitate product performance records.
o Review coding and investigations with engineering, laboratory, and other internal staff.
o Compose written communications detailing the clinical observation, investigation and/or product
analysis, and corrective actions, as applicable, to physician and other end use customers.
o Review complaint communications and assess for regulatory compliance, reportability, and potential
impact to patient safety and business operations.
o Apply clinical knowledge, as related to product application, to evaluate identified complaints.
o Investigate complaints by gathering sufficient data from clinical staff, field representatives, internal
employees, and laboratory analysis.
o Establish regulatory reportability decisions using event investigation and regulatory decision models.
o Participate in development and modification of these decision models with changes in product
advances/therapies to uphold consistent compliance with government-mandated regulations.
o Write Medical Device Reports (MDRs), MedWatch, Vigilance, and other regulatory reports, ensuring
timely transmission to the appropriate regulatory authorities.
o Apply codes to events to facilitate product performance records.
o Review coding and investigations with engineering, laboratory, and other internal staff.
o Compose written communications detailing the clinical observation, investigation and/or product
analysis, and corrective actions, as applicable, to physician and other end use customers.
o Communications include determination/eligibility for warranty credit or unreimbursed medical
payments


Please wait..!!