Join to apply for the Gerente QRA, Dirección TécnicaColombia role at Messer Americas. Messer is the largest privateindustrial gases company in the world and a leading provider ofindustrial and medical gases in North and South America. With over120 years of experience, Messer delivers gases, services, andtechnologies safely through an extensive production anddistribution network. Job Description The role involves leadingquality management and regulatory affairs in Colombia, ensuringcompliance with health and regulatory standards for medicinal gasesand medical devices. Responsibilities include obtaining andmaintaining health registrations, certifications, traceability, andimplementing quality and safety management systems to position thecompany as a sector leader. Responsibilities 1. Ensure compliancewith quality assurance activities across manufacturing plants,storage, and distribution of medicinal gases and medical devices,in accordance with Good Manufacturing Practices (GMP), MedicalHealthcare Requirements, and applicable legislation. 2. Lead andmaintain health registrations for medicinal gases and medicaldevices in the country. 3. Collaborate with operations to implementlocal and global quality and regulatory standards. 4. Supportbusiness areas according to Messer's global standards and localregulations. 5. Implement and monitor policies and strategic plansfor manufacturing, distribution, and patient-related services inthe region. 6. Oversee surveillance programs (Fármaco-Tecno). 7. Advise the legal representative on product characteristics andmarketing, ensuring compliance with current regulations. 8. Ensureongoing staff training on GMP and CCAA standards. 9. Guaranteeproduct traceability and compliance with surveillance programs formedical devices and medicines. 10. Act as the Technical Director ofMesser Colombia S.A. before health authorities. 11. Collaboratewith regulatory bodies to improve product control processes. 12. Manage personnel performance according to company standards. 13. Develop regulatory strategies for product registration andmarketing. 14. Oversee batch release processes, ensuringtraceability and proper record keeping. 15. Delegate batch releasetasks to Quality Managers as appropriate. 16. Design and implementa food safety management system under FSSC 22001 standards,ensuring continuous improvement. 17. Maintain and update the foodsafety management documentation. 18. Participate in hazardidentification and assessment for product safety. 19. Maintainupdated documentation on food safety legislation and monitor legalcompliance. 20. Coordinate food safety team meetings. HSEQResponsibilities - Use personal protective equipment according toactivity. - Apply company HSEQ procedures and standards. -Participate in HSEQ programs. - Follow HSEQ rules of the company. Qualifications - Minimum six (6) years of experience in quality andregulatory affairs, with at least four (4) years in regulatoryprocedures before INVIMA and other health entities. FormalEducation: Bachelor’s degree in Pharmaceutical Chemistry. Postgraduate: Production or quality, preferably a Master’s degree. Required Certifications: Auditor certification. Specific Knowledge:Quality assurance, implementation of quality management systems,Good Manufacturing Practices, regulatory affairs, and healthauthority procedures. Messer Americas is committed to fostering aculture that promotes diversity and inclusion. We value ouremployees as our most valuable resource and strive to develop adiverse and inclusive organization. If you meet the requirementsand are interested in joining our team, we invite you to apply andtake on this new professional challenge. #J-18808-Ljbffr