Stop TB Partnership - Quality Product Officer
Background Information - Job-specific
UNOPS hosts the Stop Tuberculosis Partnership Secretariat (STBP) as of 1 January 2015, in Geneva, Switzerland. The vision of the Stop TB Partnership is to realize the goal of elimination of Tuberculosis (TB) as a public health problem and, ultimately, to acquire a world free of TB by ensuring that every TB patient has access to effective diagnosis, treatment and cure; stopping transmission of TB; reducing the inequitable social and economic toll of TB; and developing and implementing new preventive, diagnostic and therapeutic tools and strategies. The Stop Partnership is uniquely positioned to support the development and further implementation by partners of the current and future Global Plan, acting as a coordinator and catalyst for the range of partners engaged in the fight against TB.
Founded in 2001, STBP's mission is to serve every person who is vulnerable to TB and ensure that high-quality treatment is available to all who need it. Stop TB partners include international and technical organizations, government programmes, research and funding agencies, foundations, NGOs, civil society and community groups and the private sector.
As a key initiative of the Stop TB Partnership, the objective of the Global Drug Facility (GDF), an ISO:9001:2015 certified entity, is to ensure access to quality-assured TB drugs, diagnostics, and other health products by employing innovative business approaches, efficient knowledge management for factual leadership in market management, strategic procurement, and high-quality procurement and supply services to client countries. GDF’s strategic vision of success is that all people requiring TB diagnostics and medicines can access them from markets optimized to meet public health needs.
The GDF procures all groups of medicines, key diagnostic tools and other health products that are currently recommended by WHO for diagnosis, prevention, and treatment of drug susceptible and resistant forms of TB. When procuring through GDF, countries are ensured to receive quality-assured TB products in compliance with WHO Prequalification Program or Stringent National Medicines Regulatory Authorities or the Global Fund – ERP program.
In addition, GDF applies an outstanding Drug Monitoring Program (DMP) coordinated with and performed by contracted Quality control agents which consists of the review of the manufacturer issued certificate of analysis for procured product batches, consignment pre-shipment inspection and sampling, and quality testing of product batches supplied to countries.
The Product Quality Officer will be part of the Strategic Procurement and Business Intelligence (SPBI) unit that aims to ensure timely access to quality-assured TB products appropriately adapted, affordable and sustainably priced. She/He will work under the supervision of the Lead Product Quality Officer and in close collaboration with other GDF teams and partners, to ensure that TB medicines, diagnostics and other health products procured and supplied by GDF to countries are quality assured and of adequate standard.
All activities performed by the Product Quality Officer will be implemented in accordance with the ISO9001:2015 GDF quality manual.
Work for this position calls for excellent technical and writing skills.
The Product Quality Officer will act as the GDF focal point for quality of diagnostics and other health products and will be responsible to perform the functions/tasks described below and deliver results, under the supervision of the Lead Product Quality OfficerThe main responsibilities include:
Ensure the quality of TB diagnostics and other health products such as medical devices, medical software, digital adherence tools procured and supplied to GDF client countries for the diagnosis, prevention, and treatment of drug susceptible and resistant forms of TB.
Review and update the GDF QA policy for diagnostics and other health products in compliance with applicable high-quality standards.
Develop the GDF quality monitoring program for diagnostics and other health products (DHMP) including pre-shipment inspection of consignments, sampling, and quality testing.
Contribute to the tender for selection of the quality control agents (QCAs) responsible for performing the activities related to DHMP and support contract management of QCAs.
Develop SOP and critical metrics to implement and supervise the efficiency of GDF’s QA policy and quality monitoring program for diagnostics and other health products, and identify/implement corrective and improvement actions where needed.
Work in close collaboration with manufactures and the regulatory and standardization agencies and authorities including WHO to assure quality status of diagnostics and other health products.
Maintain up to date list of eligible and quality assured diagnostics and other health products for GDF procurement.
Handle quality complaints for diagnostics and other health products.
Work with partners toward harmonization of QA policy for diagnostics and other health products and approaches to respond to countries program needs for access to quality-assured products
Support the development of GDF’s systems and processes for handling and supervising quality of TB products procured and supplied to countries.
Coordinate and support the development of the GDF web-based platform tool for efficient management and monitoring of QA status of TB products, their registration status in countries, quality product complaints and related supportive documentation
Work in close collaboration with GDF’s contracted procurement agent and other relevant partners for the implementation of the GS1 Standards for TB products.
Work with relevant partners and manufacturers for the development of the GDF’s environmental sustainability strategy that GDF will use in its strategic procurement to encourage environmentally sustainable and driven markets whilst ensuring uninterrupted access to TB products.
Document GDF results and incorporate lessons learned into new approaches (The below sub-activities are indicative)
Report on the efficiency and impact of GDF QA policy for TB products from a product, access, and cost perspective
Develop relevant indicators, dashboards, and infographics to monitor, evaluate, present and document GDF QA results and achievements against targets.
Draft reports, briefs, presentations for Board and donors
Identify key conferences where GDF can disseminate GDF QA achievements and coordinate sessions, symposia, satellites, in collaboration with key stakeholders
The Quality Product Officer will undertake other special work related to general activities within the StopTB partnership’s Global Drug Facility, assigned and determined by Stop TB’s Executive director, GDF Chief, SPBI Manager or Lead Product Quality Officer.
TB products including TB diagnostics and other health products procured and supplied by GDF to countries are quality-assured.
GDF QA’s policy and quality monitoring program for diagnostics and other health products are in force.
Bar coding is in place to ensure batch traceability for TB products procured by and supplied to countries by GDF.
GDF environmental sustainability strategy is integrated in GDF strategic procurement processes and procedures.
Advanced university degree (master's or equivalent) in pharmacy, medicine, biology, public health, or other field related to the job description.
A University Degree (Bachelor degree or Undergraduate) with additional two (2) years of experience will be considered in lieu of an advanced University Degree.Quality assurance and quality control diplomas, especially for diagnostics and/or medical devices is an asset.
A minimum of five (5) years of professional experience working in quality assurance ideally for Health Products (pharmaceuticals, and/or diagnostics and/or medical devices) including in quality control, at national and/or international level.
Highly desired experience:
Experience in developing QA policies, tools, and guidance for diagnostics and/or medical devices.
Experience in developing partnerships with UN agencies, international NGOs, and donors on QA issues.
Experience in Public Health/Procurement and Supply Chain Management (PSM) of Health Products.
Good writing skills.
Experience in managing complex situations, issues at country, regional and international level.
Experience in TB medicine and/or diagnostics and/or medical devices management.
Fluency in English is essential,
Fluency in written and spoken French is a strong asset for this selection process.
|Develops and implements sustainable business strategies, thinks long term and externally in order to positively shape the organization. Anticipates and perceives the impact and implications of future decisions and activities on other parts of the organization.(for levels IICA-2, IICA-3, LICA Specialist- 10, LICA Specialist-11, NOC, NOD, P3, P4 and above)|
|Treats all individuals with respect; responds sensitively to differences and encourages others to do the same. Upholds organizational and ethical norms. Maintains high standards of trustworthiness. Role model for diversity and inclusion. |
|Acts as a positive role model contributing to the team spirit. Collaborates and supports the development of others. For people managers only: Acts as positive leadership role model, motivates, directs and inspires others to succeed, utilizing appropriate leadership styles.|
|Demonstrates understanding of the impact of own role on all partners and always puts the end beneficiary first. Builds and maintains strong external relationships and is a competent partner for others (if relevant to the role).|
|Efficiently establishes an appropriate course of action for self and/or others to accomplish a goal. Actions lead to total task accomplishment through concern for quality in all areas. Sees opportunities and takes the initiative to act on them. Understands that responsible use of resources maximizes our impact on our beneficiaries.|
|Open to change and flexible in a fast paced environment. Effectively adapts own approach to suit changing circumstances or requirements. Reflects on experiences and modifies own behavior. Performance is consistent, even under pressure. Always pursues continuous improvements.|
|Evaluates data and courses of action to reach logical, pragmatic decisions. Takes an unbiased, rational approach with calculated risks. Applies innovation and creativity to problem-solving.|
|Expresses ideas or facts in a clear, concise and open manner. Communication indicates a consideration for the feelings and needs of others. Actively listens and proactively shares knowledge. Handles conflict effectively, by overcoming differences of opinion and finding common ground.|
Contract type, level and duration
Contract type: UN Staff - Temporary Appointment. Contract level: ICS10 - P3 equivalent.
Contract duration: Appointment with UNOPS will be valid until 31st December 2021. Possibility to extend under the new host of STBP in 2022.
For more details about United Nations staff contracts, please follow this link: https://www.unops.org/english/Opportunities/job-opportunities/what-we-offer/Pages/UN-Staff-Contracts.aspx
- Please note this position is based in Geneva, Switzerland a Family Duty Station.
- Please note that the closing date is midnight Copenhagen time
- Applications received after the closing date will not be considered.
- Only those candidates that are short-listed for interviews will be notified.
- Qualified female candidates are strongly encouraged to apply.
- Qualified candidates from TB affected countries are strongly encouraged to apply. See here the list of countries: http://www.stoptb.org/countries/tbdata.asp
- UNOPS seeks to reasonably accommodate candidates with special needs, upon request.
- Work life harmonization - UNOPS values its people and recognizes the importance of balancing professional and personal demands. We have a progressive policy on work-life harmonization and offer several flexible working options. This policy applies to UNOPS personnel on all contract types
- For staff positions only, UNOPS reserves the right to appoint a candidate at a lower level than the advertised level of the post
- For retainer contracts, you must complete a few Mandatory Courses (around 4 hours) in your own time, before providing services to UNOPS.
- The incumbent is responsible to abide by security policies, administrative instructions, plans and procedures of the UN Security Management System and that of UNOPS.
It is the policy of UNOPS to conduct background checks on all potential recruits/interns. Recruitment/internship in UNOPS is contingent on the results of such checks.
Background Information - UNOPS
UNOPS is an operational arm of the United Nations, supporting the successful implementation of its partners’ peacebuilding, humanitarian and development projects around the world. Our mission is to help people build better lives and countries achieve sustainable development.
UNOPS areas of expertise cover infrastructure, procurement, project management, financial management and human resources.
Working with us
UNOPS offers short- and long-term work opportunities in diverse and challenging environments across the globe. We are looking for creative, results-focused professionals with skills in a range of disciplines.
With over 4,000 UNOPS personnel and approximately 7,000 personnel recruited on behalf of UNOPS partners spread across 80 countries, our workforce represents a wide range of nationalities and cultures. We promote a balanced, diverse workforce — a strength that helps us better understand and address our partners’ needs, and continually strive to improve our gender balance through initiatives and policies that encourage recruitment of qualified female candidates.
Work life harmonization
UNOPS values its people and recognizes the importance of balancing professional and personal demands.