Quality Assurance Specialist
at United Nations Development Programme UNDP
København, Region Hovedstaden, Denmark -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 29 Jul, 2024 | Not Specified | 04 May, 2024 | 2 year(s) or above | Medical Devices,Specifications,Biomedical Engineering,Medical Equipment,Addition | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Job Identification
17746
Locations
Copenhagen, Denmark
Posting Date
04/22/2024, 08:12 AM
Apply Before
04/29/2024, 10:59 PM
Job Schedule
Full time
Agency
DESIRED SKILLS IN ADDITION TO THE COMPETENCIES COVERED IN THE COMPETENCIES SECTION:
- Certification in project management is an asset
- Experience/expertise in the design of medical oxygen systems is an asset.
- Work experience with a UN Agency or International NGO is an asset.
- Understanding the WHO guidance on the medical device procurement process is an asset
Required Skills and Experience
Education:
- Advanced university degree (master’s or equivalent) in Biomedical Engineering is required.
OR
- A first-level university degree (bachelor’s degree) in the above-mentioned field of study, in combination with an additional two years of qualifying experience will be given due consideration in lieu of the advanced university degree.
Experience:
- Minimum 7 years (with master’s degree) or 9 years (with bachelor’s degree) of progressive relevant experience in a broad range of hospital technologies.
REQUIRED SKILLS:
- At least 2 years relevant experience in managing or advising on medical devices including medical equipment within a hospital or supporting hospitals particularly in Low-Middle-Income-Countries (LMIC).
- Work experience supporting a developing country.
- Development of specifications of medical equipment
DISCLAIMER
Important information for US Permanent Residents (’Green Card’ holders)
Under US immigration law, acceptance of a staff position with UNDP, an international organization, may have significant implications for US Permanent Residents. UNDP advises applicants for all professional level posts that they must relinquish their US Permanent Resident status and accept a G-4 visa, or have submitted a valid application for US citizenship prior to commencement of employment.
UNDP is not in a position to provide advice or assistance on applying for US citizenship and therefore applicants are advised to seek the advice of competent immigration lawyers regarding any applications.
Applicant information about UNDP rosters
Note: UNDP reserves the right to select one or more candidates from this vacancy announcement. We may also retain applications and consider candidates applying to this post for other similar positions with UNDP at the same grade level and with similar job description, experience and educational requirements.
Non-discrimination
UNDP has a zero-tolerance policy towards sexual exploitation and misconduct, sexual harassment, and abuse of authority. All selected candidates will, therefore, undergo rigorous reference and background checks, and will be expected to adhere to these standards and principles.
UNDP is an equal opportunity and inclusive employer that does not discriminate based on race, sex, gender identity, religion, nationality, ethnic origin, sexual orientation, disability, pregnancy, age, language, social origin or other status.
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Responsibilities:
- Advise UNDP Global Health Procurement Center (GHPC) and Country Offices (COs) on a broad range of medical devices, including oxygen supply equipment and disposables to be procured according to estimated national needs and existing delivery systems for oxygen therapy;
- Advise COs in reviewing national oxygen gas consumption and medical oxygen production capacity, national technical and regulatory assessment of oxygen production, and identification of gaps and improvement plan design;
- Advise GHPC and COs in developing ToRs, technical specifications and technical evaluations for procuring the medical devices, adequate technologies for medical oxygen production and its implementation, installation/maintenance and capacity building of biomedical staff;
- Facilitate the QA team in the maintenance of the QA database of COVID medical devices, including oxygen supply equipment and disposables and in the production of QA corporate reports;
- Work with the QA Advisor to develop, revise and deliver QA training activities/packages for UNDP’s COs, GHPC and other Business Units, and guidance materials and tools, including the writing of new SOPs and development of related tools;
- Facilitate the QA Advisor in the communication related to the procurement of medical devices, including oxygen supply equipment and disposables (participation to inter-agency meetings, writing of reports);
- Represent UNDP in the relevant inter-agency technical groups e.g. medical device, medical equipment, oxygen systems, medical equipment and provide UNDP with reports of meetings.
- Advise UNDP QA Team in the technical evaluation of medical devices as needed; and
- The incumbent performs other duties within their functional profile as deemed necessary for the efficient functioning of the Office and the Organizatio
REQUIREMENT SUMMARY
Min:2.0Max:9.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Software Testing
Graduate
Biomedical engineering is required
Proficient
1
København, Denmark