Are you passionate about technology, automation, and quality in the pharmaceutical and life sciences industries? At Towa, we're looking for your talent! Join our remote team of BIOVIA specialists, developers, or validation engineers and be part of international projects in the integration, optimization, and automation of regulatory and scientific processes.
**Technical Requirements and Experience at BIOVIA**
Bachelor's or Master's degree in Computer Science, Bioinformatics, Chemistry, Life Sciences, Information Systems, or a related field.
Advanced English (verbal and technical).
Demonstrable experience with any BIOVIA platforms listed: Discoverant, Pipeline Pilot, LES, ELN, or laboratory systems (LIMS, SDMS, NuGenesis).
Proficiency in workflow development, data integration, visualization, and reporting using Pipeline Pilot, Tableau, Spotfire, and/or Denodo.
Knowledge and management of computerized systems validation under GAMP 5, 21 CFR Part 11, EU Annex 11,



GxP standards and regulatory compliance in pharmaceutical/biotech.
**Key Competencies in BIOVIA Integration, Automation, and Compliance**
Analytical skills, critical thinking, and results-focused skills.
Effective communication skills for remote work and multicultural teams.
Independent task management with a strong commitment to technical and regulatory quality.
Proactive attitude toward continuous learning and adaptation to new automation and validation technologies.
**Benefits of Working at Towa**
100% remote work.
Learning bonus and access to technical training and ongoing certification programs.
Adaptable vacations ("Towa Vacations").
Opportunities for economic and professional growth through the Talent Booster program.
Join Towa and boost your career as BIOVIA Specialist.

📌 Biovia Specialist (Developers or Validation Engineers) (Ciudad de México)
🏢 Towa
📍 Ciudad de México