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Medical Devices Consultant

JOB SUMMARY

Company USP Ghana
Industry NGO/IGO/INGO
Category Public Health
Location Accra
Job Status Contractor/Co...
Salary Attractive
Education Bachelor of P...
Experience 5 years
Job Expires Oct 06, 2021
Contact Erica Asante-...
 

Company Profile

The U.S. Pharmacopeial Convention (USP) USA is an independent scientific organization that collaborates with the world's top experts in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP brings together more than 1,100 talented professionals across five global locations to deliver its mission to strengthen the supply of safe quality medicines and supplements worldwide. USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. Employment selection and related decisions are made without regard to sex, race, age, disability, religion, national origin, color, veteran status, sexual orientation, gender identity, or any other protected class. We are committed to working with and providing reasonable accommodation to individuals with disabilities. USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under a specific written agreement with USP

Job Description

The regulation of medical devices is an essential part of regulation and hence forms a part of Regulatory systems strengthening. USP-Ghana requires the services of an expert to conduct training in the assessment of dossiers presented for medical devices.

Responsibilities:

  • Develop and update materials for the delivery of trainings in medical devices dossiers evaluation in accordance with international guidelines/standard (WHO, BSI etc.) and best practices.
  • Develop materials to cover:
  • Basic levels of control for medical devices.
  • Advanced regulatory systems for medical devices
  • Assessment of common submission dossier template
  • Summary Technical Documentation (STED) for Demonstrating Conformity to the Essential Principles of Safety and Performance of Medical Devices and
  • Common Medical Devices being employed during the COVID-19.
  • Deliver trainings in medical devices dossiers compilation and evaluation.
  • Provide hands-on coaching for dossier assessors

Required Skills or Experience

Requisites:

  • Should have background in life sciences with a regulatory knowledge and experience for at least 5 years in medical devices regulation.
  • Ability to teach with relevant examples and expertise.

How To Apply

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