Job Title: Product Surveillance Associate
Job Location: Sturtevant WI 53177
Job Duration: 12 months
Job Summary:
- The Product Surveillance Specialist performs day-to-day tasks and provides technical data assessment of post-market events.
- This position plays an integral role in maintaining compliance with global regulations.
- The Product Surveillance Specialist works with moderate supervision and requires a high degree of interaction with customers health care professionals and Global employees at all levels within the organization.
Job Responsibilities
-
Field inquiries received by phone electronic or verbal correspondence and determine if it qualifies as a complaint; document reported issues according to applicable SOP(s).
-
Provide technical support and remote troubleshooting guidance as needed.
-
Review associated records and contact users and customers to collect information on the treatment product performance functionality etc.
-
Conduct periodic follow-up to close complaints in a timely manner.
-
Manage customer relationship and expectations during the course of the complaint investigation.
-
Complete investigations which may include execution or coordination of product returns and subsequent evaluations review of manufacturing records and ensuring proper approvals are obtained as part of closure.
-
Develop solutions to a variety of basic problems.
-
Support statistical analysis of complaint trends.
-
Support training program by completing assigned training in a timely manner.
-
Support operational changes to improve efficiencies in all aspects of complaint handling.
-
Support investigations associated with product deviations product non-conformances CAPAs scrap and rework and analyzing the data for the reasons of Quality Improvement and reporting.
-
Support internal and external quality system audits.
-
Evaluate complaints and determine if the submission of a Medical Device Report (MDR) or other Vigilance Report is required.
-
Employees will be required to follow any other job-related instructions and to perform any other job-related duties required by their supervisor.
Qualifications:
Education/ Professional Experience
- High School Diploma with 3 years of experience or Associates Degree with 1 year of experience.
- Customer Service Experience. (Preferred)
- Medical or Surgical Office Experience. (Preferred)
Knowledge Skills and Abilities
- Familiar with ISO 13485 Quality System Standards FDA Quality System Regulations GMPs and/or other international medical device regulations. (Preferred)
- Basic medical and/or scientific terminology. (Preferred)
- Organized with attention to detail.
- Able to prioritize and manage multiple records/reports simultaneously.
- Professional phone etiquette with the ability to appropriately handle sensitive information.
- Good communication skills including written and verbal.
- Ability to work with company staff and communicate effectively throughout the organization.
- Experience with Microsoft Office Suite.
Job Title: Product Surveillance Associate Job Location: Sturtevant WI 53177 Job Duration: 12 months Job Summary: The Product Surveillance Specialist performs day-to-day tasks and provides technical data assessment of post-market events. This position plays an integral role in maintaining complian...
Job Title: Product Surveillance Associate
Job Location: Sturtevant WI 53177
Job Duration: 12 months
Job Summary:
- The Product Surveillance Specialist performs day-to-day tasks and provides technical data assessment of post-market events.
- This position plays an integral role in maintaining compliance with global regulations.
- The Product Surveillance Specialist works with moderate supervision and requires a high degree of interaction with customers health care professionals and Global employees at all levels within the organization.
Job Responsibilities
-
Field inquiries received by phone electronic or verbal correspondence and determine if it qualifies as a complaint; document reported issues according to applicable SOP(s).
-
Provide technical support and remote troubleshooting guidance as needed.
-
Review associated records and contact users and customers to collect information on the treatment product performance functionality etc.
-
Conduct periodic follow-up to close complaints in a timely manner.
-
Manage customer relationship and expectations during the course of the complaint investigation.
-
Complete investigations which may include execution or coordination of product returns and subsequent evaluations review of manufacturing records and ensuring proper approvals are obtained as part of closure.
-
Develop solutions to a variety of basic problems.
-
Support statistical analysis of complaint trends.
-
Support training program by completing assigned training in a timely manner.
-
Support operational changes to improve efficiencies in all aspects of complaint handling.
-
Support investigations associated with product deviations product non-conformances CAPAs scrap and rework and analyzing the data for the reasons of Quality Improvement and reporting.
-
Support internal and external quality system audits.
-
Evaluate complaints and determine if the submission of a Medical Device Report (MDR) or other Vigilance Report is required.
-
Employees will be required to follow any other job-related instructions and to perform any other job-related duties required by their supervisor.
Qualifications:
Education/ Professional Experience
- High School Diploma with 3 years of experience or Associates Degree with 1 year of experience.
- Customer Service Experience. (Preferred)
- Medical or Surgical Office Experience. (Preferred)
Knowledge Skills and Abilities
- Familiar with ISO 13485 Quality System Standards FDA Quality System Regulations GMPs and/or other international medical device regulations. (Preferred)
- Basic medical and/or scientific terminology. (Preferred)
- Organized with attention to detail.
- Able to prioritize and manage multiple records/reports simultaneously.
- Professional phone etiquette with the ability to appropriately handle sensitive information.
- Good communication skills including written and verbal.
- Ability to work with company staff and communicate effectively throughout the organization.
- Experience with Microsoft Office Suite.
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