Technical Director (Director Técnico)

The Director Técnico / Qualified Person is legally responsible for ensuring that every batch of a pharmaceutical product is manufactured and controlled according to Good Manufacturing Practices (GMP) and the product's sanitary registration.Start: April 2026Duration: 12 months (40 hrs/week)Role Scope & AccountabilityDesign, implementation of the local Quality Management System (QMS) for our client, including governance of deviations, CAPAs, change control, complaints management, and product recallsOversight of GMP and GDP compliance across all local operations, including effective quality oversight of third‑party partners and service provider in ColombiaEnsuring alignment between global Quality standards and local regulatory requirements, translating global policies into effective local executionRequirementsMust be a Químico Farmacéutico (Pharmaceutical Chemist) registered in Colombia and will be the primary point of contact with INVIMA for all technical and quality matters7-10+ years of experience (as Qualified Person as well) within GMP and GDP‑regulated biotech and/or pharmaceutical companies with demonstrated excellent hands‑on experience with both solid and sterile pharmaceutical products - within best case knowledge of our Affiliate operating modelMust be a dedicated, excellent and highly collaborative team player, demonstrating strong ownership, reliability, and the ability to work effectively across global and local stakeholdersFluency in both English and Spanish, with the capability to communicate clearly and professionally in regulatory, operational, and cross‑functional contextsProven experience working within an affiliate model as an importer, including close collaboration with distributors and external partnersDemonstrated ability to establish and operate a local Quality Management System fully aligned with both local regulatory requirements and global quality governance expectations