Consultoría (internacional) fortalecimiento sector de generacion de vacunas

Job Posting Organization:
The job posting organization is UNDP (United Nations Development Programme), which is a global development network of the United Nations. Established in 1965, UNDP operates in approximately 170 countries and territories, working to eradicate poverty and reduce inequalities through sustainable development. The organization focuses on various areas including democratic governance, peacebuilding, climate change, and disaster resilience, and aims to empower lives and build resilient nations. UNDP collaborates with governments, civil society, and the private sector to achieve the Sustainable Development Goals (SDGs).

Job Overview:
The position involves providing international consultancy services aimed at strengthening the production and quality control sector of human vaccines and other biological products. The consultant will be expected to leverage their extensive experience in the biopharmaceutical industry, particularly in the vaccine segment, to enhance the capabilities of local entities involved in vaccine production. This role requires a deep understanding of the technical and regulatory aspects of vaccine manufacturing, as well as the ability to design and implement training programs to address skill gaps in the workforce. The consultant will also be responsible for conducting assessments of technical capacities and developing strategic plans to improve production processes and compliance with international standards.

Duties and Responsibilities:

• Conduct a comprehensive assessment of the current capabilities in vaccine production and quality control within the targeted organizations.
• Develop and implement training programs aimed at enhancing the technical skills of personnel involved in vaccine manufacturing.
• Collaborate with local stakeholders to design and execute plans for improving production processes and ensuring compliance with international regulatory standards.
• Provide expert guidance on the application and validation of international regulatory norms and good practices applicable to the biological value chain.
• Evaluate and identify gaps in human capital within regulated industrial environments and propose actionable solutions.
• Prepare detailed reports and documentation of findings, recommendations, and progress made during the consultancy period.
• Engage with international partners and organizations to share best practices and foster collaboration in the field of vaccine production.

Required Qualifications:
The ideal candidate must possess a professional degree in Health Sciences, Natural Sciences, Chemical Engineering, Biochemical Engineering, Biomedical Engineering, Biotechnology, Pharmaceutical Chemistry, Microbiology, Biology, Industrial Engineering, Process Engineering, or Biotechnology Engineering. Additionally, a postgraduate degree (Master's or Doctorate) in any relevant field is required. Candidates should have a minimum of ten (10) years of specific experience in the biopharmaceutical industry, particularly in the vaccine or biological segment, with at least two years of international experience. This extensive background should demonstrate a strong understanding of production, quality control, and regulatory compliance in the biopharmaceutical sector.

Educational Background:
Candidates must have a professional degree in one of the specified fields related to health sciences or engineering. A postgraduate degree, such as a Master's or Doctorate, is also required, indicating advanced knowledge and expertise in relevant areas. This educational background is essential to ensure that the consultant has the necessary theoretical and practical knowledge to effectively contribute to the strengthening of vaccine production and quality control processes.

Experience:
The position requires a minimum of ten (10) years of experience in the biopharmaceutical industry, specifically within the vaccine or biological production segment. Out of this experience, at least two years must be in an international context, demonstrating the ability to work in diverse environments and understand global standards and practices. The candidate should have a proven track record of working on projects related to production, quality assurance, and regulatory compliance in the biopharmaceutical sector.

Languages:
Proficiency in English is mandatory, with intermediate to advanced certification required. If the candidate is a native English speaker, certification is not necessary. This language requirement is crucial for effective communication and collaboration with international stakeholders and for understanding complex regulatory documents and guidelines.

Additional Notes:
The consultancy assignment is for a duration of three months. This position is classified as an individual contractor role, and candidates are expected to submit their proposals directly through the UNDP Quantum supplier portal before the specified deadline. It is important to note that all submissions must adhere to the New York time zone for deadlines. Candidates are encouraged to create a draft response in the system to receive notifications of any changes to the tender requirements. For any clarifications, inquiries must be submitted in writing through the portal's messaging functionality by the specified date.