Consultoría (internacional) para el fortalecimiento en el sector de la producción y control de calidad de vacunas humanas y otros biológicos

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 collaborates with governments, civil society, and the private sector to achieve the Sustainable Development Goals (SDGs).

Job Overview:
This 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 expertise in areas such as chemical engineering, biochemistry, biotechnology, pharmaceutical chemistry, microbiology, or pharmacy. The role is critical in enhancing the capabilities of the biopharmaceutical industry, particularly in the context of vaccine production. The consultant will work on developing strategies and frameworks that align with international standards and best practices in vaccine production and quality assurance. The assignment is set for a duration of five months, during which the consultant will engage in various activities including assessments, training, and the development of operational guidelines.

Duties and Responsibilities:
The consultant will be responsible for a comprehensive set of duties including: conducting assessments of the current capabilities in the production and quality control of vaccines; designing and implementing training programs to address identified gaps in technical skills; developing frameworks for quality assurance and compliance with international regulations; collaborating with stakeholders in the biopharmaceutical sector to enhance production processes; providing expert advice on the latest trends and technologies in vaccine production; and preparing detailed reports and publications on findings and recommendations. Additionally, the consultant will be expected to engage in public policy discussions related to human talent in health and biotechnology, and contribute to the development of organizational structures that support effective vaccine production.

Required Qualifications:
Candidates must possess a Master's or Doctorate degree in relevant fields such as biopharmaceutical industry, biotechnology, or human talent management in vaccine production. Furthermore, certification in international GMP (Good Manufacturing Practices) regulations applicable to vaccine production from recognized regulatory authorities such as the FDA, EMA, or WHO is mandatory. The role requires a deep understanding of the biopharmaceutical landscape and the ability to navigate complex regulatory environments.

Educational Background:
The educational background required for this position includes advanced degrees (Master's or Doctorate) in disciplines related to the biopharmaceutical industry, biotechnology, or similar fields. This educational foundation is essential for understanding the complexities of vaccine production and quality control processes.

Experience:
A minimum of 10 years of specific experience in the international biopharmaceutical industry, particularly in the vaccine segment, is required. This experience should encompass areas such as production, quality control, research process development, quality assurance, pharmaceutical engineering, and continuous process improvement. Within this 10-year experience, at least 3 years must be dedicated to diagnosing technical capabilities, designing training plans, evaluating human talent gaps, and understanding the complete value chain in the production of biologicals, particularly vaccines.

Languages:
Fluency in Spanish is mandatory for this position, as the role involves communication and collaboration with local stakeholders and regulatory bodies. Proficiency in additional languages may be considered an asset, particularly English, as it may facilitate broader communication within the international biopharmaceutical community.

Additional Notes:
This consultancy position is structured as a contract for a duration of five months. It is essential for candidates to be aware that the role may involve working with international teams and stakeholders. The position is classified as an individual contractor role, and candidates should be prepared to engage in a flexible work environment that may require travel or remote collaboration. Compensation details and benefits will be discussed during the interview process.