Role Description The international expert will work with UNFPA RH NP A and national MOHMI specialists on adoption of treatment protocols including the following stages: - Assessment and revision phase - 10 working days - Desk review of existing local treatment protocol for breast cancer, identify gaps and provide recommendations. - Conduct 1 (one) online technical meeting to present evidence-based desk review results to national oncologists. - Support update of breast cancer protocol to align with WHO standards and international good practices. - Conduct 3 days online training with national specialists on the updated clinical protocol. - Methodology development - 5 working days - Develop a manual peer-review methodology for clinicians to assess adherence to protocols as a part of the quality assurance cycle, including clinical compliance indicators for national monitoring and internal audit. - Conduct a one day online workshop with national specialists on manual peer-review methodology and clinical compliance indicators. - Reporting phase - 3 working days - Develop a final consultancy report and set of related documents. Duration and Working Schedule - The Duration of this consultancy is 18 working days, from August 10th to November 30th 2026 including operational closure of the contract. Dates may vary due to availability of the expert and the national partners. Outcomes and Deliverables - Deliverable 1: Assessment Report, including a desk review of current protocols, a summary of technical recommendations from online meetings, and the first draft of updated clinical protocols for breast cancer aligned with WHO standards developed by August 30th. - Deliverable 2: 3-day online training conducted for national specialists on the updated clinical protocols by September 25th. - Deliverable 3: A complete package consisting of the set of Manual peer-review methodology clinical compliance indicators developed by October 20th. - Deliverable 4: One day online workshop for national partners on Manual peer-review methodology and clinical compliance indicators conducted by November 10th. - Deliverable 5: Final consultancy report developed by November 25th. Monitoring and Progress Control - The UNFPA Programme Analyst on Reproductive Health will monitor the International Consultant’s work through reviewing submitted materials. - The consultant will provide an update on a weekly basis on progress, challenges encountered, and support requirements. Ethical Considerations - UNFPA requires its consultants to adhere to ethical principles and standards when doing research. - The selected consultant should clearly identify any potential ethical issues and approaches, as well as the processes for ethical review in the inception report. National Ownership - The involvement of appropriate national partners will be a critical condition for the development of all the mission outcome materials in ensuring stakeholder ownership and its subsequent utilisation. Supervisory Arrangements - The International Consultants will directly work under the supervision of and report to the UNFPA Programme Analyst on reproductive health, along with the overall guidance from the UNFPA Head of Office. Expected Travel - Travel is not expected under this consultancy. Required Expertise, Qualifications, and Competencies - Advanced degree in medical sciences (Oncology and Mammology). - Qualified oncologist possessing minimum 7 years of relevant experience in the area of breast cancer treatment. - Knowledge of existing WHO recommendations and good practices as well as evidence collected by research institutions and societies. - Experience in development of protocols, clinical guidances or recommendations, methodologies. - Fluency in Russian or English. - Familiarity and experience with the Central Asian context is an asset. Inputs / Services to be Provided by UNFPA - UNFPA will provide the consultant with all the necessary materials, data, information, and available reports. - The UNFPA Country Office will put together a list of core sources and readings before the start of the consultancy. Other Relevant Information - The consultancy fee will be calculated based on the P-4 level of the UN Salary Scale for Professional and higher categories effective 1 January 2026 and will be paid in a lump sum upon successful completion of deliverables. - UNFPA provides a work environment that reflects the values of gender equality, diversity, integrity and healthy work-life balance. - We are committed to ensuring gender parity in the organization and therefore encourage women to apply. - Reasonable accommodation may be provided to applicants with disabilities upon request, to support their participation in the recruitment process. - Persons with disabilities, and individuals of other underrepresented groups are highly encouraged to apply. - UNFPA promotes equal opportunities in terms of appointment, training, compensation and selection for all regardless of personal characteristics and dimensions of diversity.

• Drive the development, maturity, and execution of UpGuard’s InfoSec Governance, Risk, and Compliance function, with primary ownership over technology and cybersecurity risk. • Partner closely with procurement, legal, and business stakeholders to embed security reviews into the purchasing lifecycle. Lead Third-Party Risk Management (TPRM) evaluations for new and existing vendors. • Review security exhibits, Data Processing Agreements, and security questionnaires during procurement negotiations to safeguard UpGuard and its customers. • Partner with the CISO to contribute expert analysis on broader enterprise and operational risk matters, ensuring a unified approach to risk management. • Architect and run the technology and security components of the Risk Management process. You will maintain, continually improve, and deliver executive-ready reporting on trends, vulnerabilities, and strategic insights. • Formally own the technology and security control components of UpGuard’s annual SOC 2 Type II audit cycle. Design, manage, and coordinate remediations and improvements stemming from prior cycles, incident post-mortems, and internal assessments. • Work cross-functionally with the Product team to develop public-facing trust documentation, while identifying security control gaps and improvement opportunities within the Product Development Life Cycle (PDLC). • Draft, implement, and maintain a robust framework of InfoSec policies, standards, processes, and guidelines tailored to an evolving threat landscape. • Design and implement comprehensive, company-wide security awareness and compliance training programs utilizing the MindTickle platform.

• Produce a complete supply risk map of every active SKU in Haircare, Body, and Fragrance within your first 90 days • Serve as the internal final approval authority on all artwork going to suppliers • Own all tech transfers across Haircare, Body, and Fragrance end to end • Conduct a full SKU documentation audit within your first 30 days • Build and maintain an approved formula library • Catch quality concerns at the development stage before production starts • Own regulatory and quality compliance across Target, Ulta, Walmart, and TikTok Shop • Conduct regular GMP, ISO, and REACH audits of manufacturers and testing facilities • Author and maintain the SOPs that keep the regulatory and tech transfer function running • Serve as the primary point of contact for all adverse event investigations in the Consumables portfolio • Use AI tools to accelerate regulatory research, SOP drafting, gap analysis, and documentation review.

Ensure compliance with U.S. export and import control laws, review product documentation for classification, and process government license applications while collaborating with internal teams and external partners to resolve compliance issues.