Developing microbiome therapies as precision medicine.


We have assembled a solid and experienced team with scientific leaders in the microbiome and probiotics field to develop novel class products.

Claudio Hidalgo Cantabrana, PhD


Noelia Martínez, PhD


Rafael M. Permuy, MBA

Board Member

Luis Buznego

Board Member

Manuel Monge

Board Member

Luis Prieto Jiménez

Board Member

Mehdi Chouikh Skalli

Board Member

José Vigaray Conde, MD

Board Member

Francisco Morís, PhD

Board Member

Abelardo Margolles, PhD

Scientific Advisor and co-founder
Professor of Research at IPLA-CSIC

Susana Delgado, PhD

Scientific Advisor and co-founder
Principal Investigator at IPLA-CSIC

Borja Sánchez, PhD

Scientific Advisor and co-founder
Principal Investigator at IPLA-CSIC

Claudio Hidalgo Cantabrana, PhD

Chief Executive Officer and co-founder

Rafael M. Permuy, MBA

Chief Business Officer and co-founder

Noelia Martínez, PhD

R&D director and co-founder

Rosa del Campo, PhD, MD

Scientific Advisor
Microbiologist at Hospital Ramón y Cajal, Madrid, Spain

Carlos López Otín, PhD, MD

Scientific Advisor
Professor at University of Oviedo, Spain

Josbert J. Keller, MD, PhD

Scientific Advisor
Gastroenterologist at Haaglanden Medical Center
The Hague, Netherlands.

Luis Gosálbez, PhD, MBA

Business Advisory Board
Managing Director at Sandwalk BioVentures

Claudio Hidalgo Cantabrana, PhD

Chief Executive Officer and co-founder

Noelia Martínez, PhD

R&D Director and co-founder


David Ríos Covián, PhD

Director of Technology Development

Rafael M. Permuy, MBA

Chief Business Officer and co-founder

Desirée Barrientos

Research Assistant

Ignacio Alberti

Sales & Business Development

Ignacio Montero, PhD

Computational Biologist

Manuel Arenal, MBA

Accounting and administration

Marta Fernández Gosende, MS

Research Intern

Pilar Manrique Ronquillo, PhD

Research Scientist

Alejandro Ojeda

Alejandro Ojeda Suárez

Lab Technician


Solid and innovative team

We want to revolutionize the microbiome and probiotics field, and to fulfill this commitment we need intelligent and hardworking people with the desire to join a dynamic team.

Talent, diversity and equality are the core values of our recruitment process and we are continuously looking for motivated people to join our company.

Job description
We are looking for a full-time, highly motivated individual to work as a Quality Assurance CMO specialist with cGMP experience for novel biotherapeutic products.

About Microviable
Microviable Therapeutics is a preclinical stage biotech company developing a novel class of orally administered biological drugs based on microbiota-derived products. Microviable is developing unique products based on complete microbiota ecosystem products and rationally defined and designed bacterial consortia, to address unmet challenges in human diseases. The current pipeline includes preclinical data for our lead candidate seeking to initiate cGMP manufacturing for first-in-human clinical trials.

We are seeking a Quality Assurance specialist with experience in biological drugs manufacturing at cGMP to assist with the development and implementation of QA documentation in a new facility, monitor QA of the manufacturing process and supervise the already implemented ISO certifications of the company.


  • Create, review, implement, approve, and maintain QA documentation
  • Provide QA oversight to ensure quality and cGMP compliance of manufacturing process
  • Batch record review and deviation management (creation, review, feedback)
  • Prepare and review API, raw materials, bulk, and finish product release specifications
  • Review and approval of pharma bulk and packaged batch records
  • General compliance activities to support on-site inspections
  • Develop and implementation of CAPA plans
  • Assists in development of appropriate Standard Operating Procedures, laboratory data collection & documentation systems (paper and electronic) and training of personnel to ensure cGMP compliance
  • Support ongoing programs and supervise current ISO certifications
  • Assist the technical team on daily QA items
  • Communicate with the team and ensure QA implementation across the organization and activities


  • More than 3 years of QA experience in a GMP environment in the pharma industry
  • Strong experience on manufacturing and related QA
  • Proven ability to develop and implement QA strategies
  • Experience generating manufacturing documentation and product data sheets
  • Knowledgeable on EU regulations for GMP manufacturing
  • Ability to work independently with minimal supervision.
  • Willingness to work collaboratively in a team environment
  • Highly motivated and organized
  • Fluency in Spanish and English


Incentives to Innovative Projects 2023

Project “New Bioactive Ingredients for cosmeceutical applications” Granted by Ayto. de Gijón. Program: Incentives to Innovative Projects 2023 – Business Cooperation Platforms.