Consultoría (nacional) para el fortalecimiento en el sector de la generación de vacunas

Consultoría (nacional) para el fortalecimiento en el sector de la generación de vacunas

United Nations Development Programme (UNDP)

February 3, 2026February 17, 2026Colombia
Job Description
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 works in about 170 countries and territories, helping 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 operates with a mission to support countries in achieving the Sustainable Development Goals (SDGs) and to promote human development and dignity.

Job Overview:
The position involves providing national consultancy services aimed at strengthening the vaccine generation sector in Colombia. The consultant will be expected to leverage their expertise in the biopharmaceutical industry, particularly in the area of vaccines or other biological products. The role requires a comprehensive understanding of production, quality control, process development, and research and development (R&D) within regulated industrial environments. The consultant will also be responsible for assessing technical capabilities, designing training plans, and evaluating human capital gaps in the industry. This position is crucial for enhancing the capacity of the vaccine sector, ensuring compliance with international regulatory standards, and improving overall process efficiency.

Duties and Responsibilities:
  • Conduct a thorough assessment of the current capabilities in the vaccine generation sector, identifying strengths and weaknesses.
  • Develop and implement training programs aimed at enhancing technical skills within the workforce.
  • Collaborate with stakeholders to design and improve processes related to vaccine production and quality assurance.
  • Provide expert advice on regulatory compliance and best practices applicable to the biopharmaceutical value chain.
  • Facilitate workshops and training sessions to disseminate knowledge and improve operational practices.
  • Monitor and evaluate the effectiveness of implemented strategies and training programs, making adjustments as necessary.
  • Prepare detailed reports and documentation of findings, recommendations, and progress made during the consultancy period.
  • Engage with international regulatory bodies to ensure alignment with global standards and practices.

Required Qualifications:
Candidates must possess a professional degree in relevant fields such as Health Sciences, Natural Sciences, Chemical Engineering, Biochemical Engineering, Biomedical Engineering, Biotechnology, Pharmaceutical Chemistry, Microbiology, Biology, Industrial Engineering, or Biotechnology Engineering. Additionally, candidates should have postgraduate studies (master's or doctorate) in any area of knowledge. A minimum of 6 years of specific experience in the biopharmaceutical industry, particularly in the vaccine segment or other biologicals, is required. This experience should demonstrate work in areas such as production/manufacturing, quality control or assurance, process development, R&D, or specialized logistics.

Educational Background:
The educational background required for this position includes a professional degree in one of the specified fields related to health or natural sciences, along with postgraduate qualifications such as a master's or doctoral degree. This advanced education is essential to ensure that the consultant has the necessary theoretical knowledge and practical skills to effectively contribute to the vaccine generation sector.

Experience:
Candidates should have at least 6 years of relevant experience in the biopharmaceutical industry, specifically within the vaccine sector or related biological products. This experience should encompass various aspects of the industry, including production, quality assurance, process development, and regulatory compliance. The consultant should have a proven track record of working in regulated environments and should be familiar with the challenges and requirements of the biopharmaceutical sector.

Languages:
Fluency in Spanish is mandatory, and candidates should also possess intermediate to advanced proficiency in English, supported by a certification. This bilingual capability is essential for effective communication with diverse stakeholders and for understanding international regulatory standards.

Additional Notes:
The consultancy assignment is expected to last for a period of 4 months. This position is classified as an individual contractor role, and candidates should be prepared to submit their proposals through the UNDP Quantum supplier portal before the specified deadline. It is important to note that the time zone for submissions is New York time. Candidates are encouraged to clarify any questions through the messaging functionality in the portal before the deadline for inquiries. The position is open to national consultants, and all proposals must be submitted directly through the designated portal.
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