Engineer and Biomedical Engineer – Senegal

A. Conception and staging of a complete set of strategies

Consultant of the partner organization, head of the project and/or person responsible for carrying out steps at the port of the project, technical requirements/essential global fundamentals based on the tasks of partners and beneficiaries, in addition with regard to requirements and standards National and international certification for the equipment, associated services and work include the best practices.
Auditor, consultant and assistant in the consolidation of equipment lists depending on the type of service. The auditor makes his operational and business recommendations to the project concerned and other parties based on the specifications and other required techniques/needs for developers, planners, launchers, etc. Governance de la passation de marchés de l’UNOPS (Rules, Regulations, Policies and Tools).
The preparation of technical specifications covers the post-installation services and the provision of quantitative data in the tender documents for the healthcare professionals to be acquired as part of a project.
Organizing and monitoring logistics for shipping, installation, training and service for medical supplies.
Preparation of a calendar of requirements, conditions, evaluation criteria and exact documents required before placing the order.

B. Appui à la gestion des Processus d’achats de dispositifs medicaux

When identifying specialists and tenants, the requirements for technology, quality and durability are taken into account in order to satisfy the partners’ attention as much as possible.
Participant in the evaluation/membership in the evaluation of offers/proposals for the establishment of biomedical equipment and related services and works.
Note that the modalities and specific requirements for carrying out processes are appropriate to the needs of each case and that you must rely on a knowledge of the policies and instruments for carrying out medical measures at UNOPS, etc. According to good practices.
Assist us in working near you and controlling the process of project implementation, including organizing application documents, your evaluation, negotiating certain contract terms and compliance with all rules and regulations of UNOPS regarding the passage of markets.
We support you in ensuring that the contracts and contracting parties are managed optimally through the bias of the service providers and the contracts according to the agreed reference criteria and through the bias of the reporting mechanisms Konvenus.

C. Quality assurance

Ensures compliance with specific quality and durability requirements of UNOPS policy and medical device industry good practice.
Verify and validate the conformity of the biomedical device with the specifications before installation and operation.
Supervise the installation of equipment/systems, ensure quality assurance and ensure that required work is carried out in accordance with design specifications and installation contracts.
Check the performance of medical devices/systems, review reports and ensure that all maintenance is under warranty.
Prepare operation and maintenance plans for all equipment/systems installed as part of the project and communicate them to the customer for project success.

D. Monitoring and control

Preparation of regular reports: work progress based on calendars and created plans, agreement problems, solutions, planning of activities for the next week.
The participant, led by his/her manager, informs the editorial staff of various reporters that he/she has identified each project concerned as part of the communication plan for the project(s).
Assistance in certifying the progressive payment requests of the entrepreneur who deals with medical equipment and related services.
Supervising the training of medical personnel, exploitation and maintenance work and the management of files.
Supervision of work and work in the service of medical devices/systems for the final installations, as well as preparation of reports for the service and return for the customer.
Promoting and maintaining projects within the country’s medical equipment park involves identifying synergies and expansion opportunities as they happen.

E. Strengthening capacities and knowledge share

Organizer, facilitator and/or promoter of education and training initiatives for personnel focused on issues related to the procurement of medical supplies.
The client is responsible for initiatives to develop capacities and knowledge for the responsible staff and includes the development of resources, plans, plans and teaching activities as well as information on practical work with case workers, etc. “Comparative assessment of the meilleures pratiques.”
Contributor to knowledge bases and communities of practice, as well as medical device knowledge.
Lead the gathering of information, ideas and insights within the process, definitions and best practices and the productive use of manners for lasting solutions for partners.

How to apply