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Position Summary: We are seeking a Technical Director to lead regulatory affairs, quality management systems, and product development within a manufacturing company. Key Highlights: 1. Leadership in regulatory affairs before INVIMA and compliance with current regulations. 2. Design and implementation of Quality Management Systems (GMP). 3. Innovation and development of new functional foods and dietary supplements. A manufacturing-sector company requires: TECHNICAL DIRECTOR for Pereira. · COUC Code: 22620 · Skills: reading comprehension, written communication, assertive communication, critical thinking, applied learning, activity evaluation and control, teamwork, complex problem solving, needs analysis, quality control analysis. · Responsibilities: 1. Serve as Technical Director before INVIMA, signing and assuming responsibility for sanitary registrations, mandatory sanitary notifications (MSN), and all regulatory filings for products manufactured at the facility, ensuring compliance with current regulations (Resolutions 3168/1996, 2674/2013, and other applicable regulations). 2. Design, implement, and maintain the facility's Quality Management System (QMS) under Good Manufacturing Practices (GMP) standards for food and dietary supplements, leading internal and external audits as well as health authority inspections (INVIMA, Municipal and Departmental Health Secretariats). 3. Supervise and approve formulations, production processes, technical specifications for raw materials, packaging materials, and finished products, ensuring safety, stability, and compliance with physicochemical and microbiological requirements for all products. 4. Lead the innovation and development process for new functional foods and dietary supplements—from scientific conceptualization and formulation through process validation to obtaining sanitary registration or notification before INVIMA. 5. Manage and approve all technical system documents: Standard Operating Procedures (SOPs), validation protocols, sampling plans, HACCP risk analyses, and process control matrices. 6. Coordinate with production, quality, logistics, and commercial departments to ensure efficient operational flow under the highest standards of quality, safety, and current sanitary regulation. 7. Represent the company technically before regulatory bodies, certification agencies, and high-level clients requiring scientific support or third-party audits. · Educational Requirement: Pharmaceutical Chemist (professional degree required by INVIMA) Required Knowledge: GMP (Resolution 2674/2013), ISO 22000, HACCP, INVIMA regulations for food and dietary supplements, quality management systems, pharmacovigilance and technovigilance, national sanitary legislation. Experience: Minimum 2 years in similar roles within food, dietary supplement, or pharmaceutical manufacturing facilities. Contract Type: Indefinite-term contract. Salary: $4,500,000 COP + social benefits. Working Hours: Monday to Friday, 8:00 a.m. to 5:00 p.m., with a 1-hour lunch break. -Requirements- Minimum Education: University / Professional Degree 2 years of experience Keywords: leader, head, manager, director, chief, lead, leadership, regent, technologist, technician, tech, technician, technology, technology, technologist, pharmacologist, pharmacist, apothecary, pharmacist, boticario
