Biotechnology Associate & Cell Manufacturing Technologist · CellGenic
A Biotechnology graduate with hands-on experience in GMP-compliant cellular manufacturing, procurement, and supply chain coordination, Diana Navarrete Landero was part of the founding team that established CellGenic — Cellular Institute’s in-house GMP cell manufacturing facility in Cancún. Her unique combination of laboratory expertise, cross-cultural communication, and operational logistics makes her a cornerstone of CellGenic’s daily manufacturing and supply operations.
Diana Teresa Navarrete Landero
CellGenic Laboratory, Cancún
Diana Teresa Navarrete Landero holds a Bachelor’s Degree in Biotechnology from Universidad Anáhuac Cancún and brings a distinctly international perspective to her scientific work. She participated in the ERASMUS+ BIP Butterfly Project at Zealand Academy in Roskilde, Denmark — a cross-cultural innovation program focused on sustainability and circular economy models — and completed a semester exchange at Universidad Anáhuac Mexico (North Campus). Before joining CellGenic, she built a multidimensional professional foundation: from andrology laboratory work at New Life México and coral reef conservation at UNAM’s Institute of Marine Sciences, to medical tourism coordination at IREGA and F&B laboratory support at Kunko Súper Yerba Mate.
Since May 2025, Diana has been part of CellGenic — the Global Stem Cells Group’s Cancún division — where she holds one of its most foundational achievements: as part of the team that coordinated the establishment of a GMP cell manufacturing facility in Mexico. Her daily work spans the full manufacturing cycle of Wharton’s Jelly-derived Mesenchymal Stem Cells (WJ-MSCs), procurement and supply chain coordination, regulatory documentation, and marketing collaboration.
Diana’s background is unusually broad for a laboratory scientist — and that breadth is precisely what makes her invaluable at CellGenic. Her experience in CRM at IREGA, market research at Kunko, environmental project management at Centinelas del Agua, and cross-cultural leadership at ERASMUS+ all converge in a role that demands not just aseptic technique, but also procurement coordination, supply chain oversight, regulatory documentation, and interdepartmental collaboration with the marketing team.
Her scientific passion is grounded in a clear vision: leveraging biotechnology to drive regenerative medicine applications within a fast-growing, innovation-first industry. As one of the scientists who helped bring CellGenic’s GMP facility to life in Mexico, Diana is not just a technician — she is a co-architect of the laboratory infrastructure that makes Cellular Institute’s cellular therapies possible.
Expert in aseptic manufacture of Wharton’s Jelly-derived Mesenchymal Stem Cells (WJ-MSCs) under GMP protocols — including media preparation, expansion, passaging, cryopreservation, thawing, and cell harvesting for regenerative medicine applications.
Oversees procurement logistics and supply chain for biological materials, reagents, and laboratory supplies — managing both commercial and internal stock, identifying trusted suppliers, and coordinating import/export of temperature-sensitive materials.
Maintains batch records, SOPs, and laboratory activity documentation in full GMP and COFEPRIS compliance — supporting quality management systems and traceability for every cellular product manufactured at CellGenic.
Actively identifies emerging technologies, novel biological materials, and entrusted suppliers to foster innovation and drive strategic growth at CellGenic — bridging scientific advancement with operational and commercial opportunity.
ERASMUS+-trained in cross-cultural communication and intercultural project leadership. Experienced working in diverse international environments — from Danish innovation labs to reef conservation projects and multinational biotech supply chains.
Collaborates with the GSCG marketing department to create educational and promotional content about cellular therapy — bridging laboratory science with patient-facing communication for Cellular Institute’s global audience.
"Leveraging biotechnology
to drive regenerative medicine forward."
One of Diana’s most significant professional achievements is her role in coordinating the establishment of CellGenic’s GMP cell manufacturing facility in Cancún — one of the few certified in-house cellular manufacturing labs in Latin America. From supply chain setup and equipment procurement to documentation systems and regulatory alignment with COFEPRIS, her contributions were part of the foundational work that gave Cellular Institute a proprietary laboratory capability that sets it apart from any other regenerative medicine clinic in the region. This GMP facility is what allows CI to manufacture cellular products in-house, under full biological control — ensuring traceability, quality, and scientific precision from cell to patient.
CellGenic is one of the only clinics in Latin America with a fully certified in-house GMP laboratory. Diana was part of building it. That’s not a credential on paper — it’s a lived understanding of what it takes to create and maintain a manufacturing environment that meets the highest biological and regulatory standards available.
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