The Technical Director/Regulatory Affairs Manager for Colombia will lead, manage, and provide strategic direction to develop and execute regulatory strategies and plans for the products of the company's portfolio. Furthermore, as Technical Director, they are the sanitary responsible and representative of the company before the Health Authority INVIMA and the Health Ministry, assuring the compliance of all quality, regulatory, and promotional activities of the company with the sanitary laws in force related to synthesis, biologic, and biotechnological products commercialized by the company. This role reports to the General Director. Job Responsibilities Lead and manage the development of regulatory strategies to support the registration of new products, line extensions, major variations, and lifecycle management. Provide strategic contribution to the country leadership team; anticipate what regulatory needs to contribute to achieving business objectives. Communicate in an effective way the regulatory approvals, denials, requirements, or issues to define a conjunct strategy. Lead the company's SGC ISO 9001 V 2015, ensuring the maintenance of processes and consolidating information from the management review, ensuring the preservation of certification. Be the responsible person before the regulatory agency for all the quality and regulatory issues to be in sanitary compliance. Relationship and management with 3PL. Liaison with personnel responsible for regulatory affairs of our international strategic allies. Minimum Skills Required Leadership Strategic Mindset Planning & Control Driven Results Team Working & Collaborative Work Effective Negotiation Minimum of 1 to 3 years of experience in the position or similar positions is required, with knowledge of drug development, rules, regulations, and guidelines. English: 2B level Other Conditions Indefinite term contract Non-integral salary Conditions of law Prepaid medical assistance for the employee Other benefits #J-18808-Ljbffr