INCL - 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 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:
This position involves providing international consultancy services aimed at strengthening the production and quality control sector of human vaccines and other biologicals. The consultant will be expected to leverage their extensive experience in the biopharmaceutical industry, particularly in the vaccine segment, to enhance the capabilities of the organization. The role requires a deep understanding of the production processes, quality assurance, and regulatory compliance in the biopharmaceutical field. The consultant will also be responsible for diagnosing technical capabilities, designing training plans, and evaluating human capital gaps in regulated industrial environments. This position is crucial for ensuring that the organization meets international standards and best practices in the production of biologicals.

Duties and Responsibilities:
The consultant will be responsible for the following duties and responsibilities:

• Conduct a comprehensive assessment of the current production and quality control processes for vaccines and other biologicals.
• Develop and implement strategies to enhance production efficiency and quality assurance measures.
• Provide expert guidance on regulatory compliance and international standards applicable to the biopharmaceutical industry.
• Design and facilitate training programs aimed at improving technical skills and knowledge among staff involved in the production and quality control processes.
• Collaborate with various stakeholders to identify and address gaps in human capital and technical capabilities.
• Prepare detailed reports and documentation outlining findings, recommendations, and action plans.
• Ensure that all activities are aligned with the organization's mission and objectives, and contribute to the overall improvement of the biopharmaceutical sector.

Required Qualifications:
The ideal candidate must possess a professional degree in related fields such as Health Sciences, Natural Sciences, Chemical Engineering, Biochemical Engineering, Biomedical Engineering, Biotechnology, Pharmaceutical Chemistry, Microbiology, Biology, Industrial Engineering, or Biotechnology Engineering. Additionally, a postgraduate degree (master's or doctorate) in any relevant area of knowledge is required. The candidate should have a minimum of ten (10) years of specific experience in the biopharmaceutical industry, particularly in the vaccine segment or other biologicals, with at least two years of international experience. This extensive background is essential to ensure the consultant can effectively contribute to the organization's goals.

Educational Background:
Candidates must have a professional degree in one of the specified fields related to health sciences or engineering. Furthermore, a postgraduate qualification such as a master's or doctoral degree in any relevant discipline is mandatory. This educational background is crucial for understanding the complex scientific and regulatory aspects of vaccine production and quality control.

Experience:
The position requires a minimum of ten (10) years of experience in the biopharmaceutical industry, specifically within the vaccine segment or other biologicals. 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 control, and regulatory compliance in the biopharmaceutical sector.

Languages:
Proficiency in English is mandatory, with intermediate to advanced certification required. This language skill is essential for effective communication and collaboration with international stakeholders and for understanding complex regulatory documents. Knowledge of additional languages may be considered an asset but is not mandatory for this position.

Additional Notes:
The assignment period for this consultancy is four months. The consultant will be engaged as an individual contractor under the procurement process of UNDP. The proposals must be submitted directly through the Quantum portal before the specified deadline. It is important to note that the time zone for submissions is New York time. Any clarifications regarding the proposal must be submitted in writing through the messaging functionality in the portal by the specified date. The consultant is encouraged to indicate their intention to submit a proposal by creating a draft response in the system, which will allow for notifications in case of any changes to the tender requirements. The position is full-time and involves international consultancy work.