Product Surveillance Associate

Pacer Group

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profile Job Location:

Sturtevant, WI - USA

profile Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

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...
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Key Skills

  • Marketing
  • Quality Assurance
  • Agile
  • Product Demos
  • Analysis Skills
  • Jira
  • Project Management
  • Product Management
  • Qualitative Analysis
  • Confluence
  • Internet Of Things
  • Product Development