### **Quality Management System (QMS) Documenter** **Location:** Zapopan, Jalisco **Position Objective** Develop, control, and maintain up-to-date documentation for the Quality Management System (QMS), ensuring consistency, validity, and compliance with the requirements established by the standards **NOM\-241\-SSA1** and **ISO 13485**. Ensure that all documentation meets applicable internal and regulatory standards, promoting continuous improvement and process efficiency. * ️ **Main Responsibilities** * Develop, review, and update QMS documents (manuals, procedures, work instructions, and records). * Coordinate and maintain the technical and functional documentation required by different company departments. * Control the distribution, storage, and safeguarding of **controlled and original copies** of the QMS. * Verify that the documentation used is **authorized and current**, preventing the use of obsolete versions. * Support the **verification of the document system**, ensuring its proper updating. * Develop and maintain updated **master lists of documents** and system records. * Advise and support departments in the correct application of internal documentation and regulations. * Assist in activities arising from **internal and external audits**, follow-up on **non-conformities**, and **corrective/preventive actions**. * Collaborate in the development of **process maps** and supporting technical documentation. * Comply with **Good Manufacturing Practices (GMP)** and organizational procedures. **Position Profile** **Education:** Bachelor's degree in Chemical Engineering, Chemistry and Pharmaceutical Biology, Chemistry, or related field. **Experience:** 2 to 3 years in roles related to documentation, quality, or regulatory compliance within regulated industries (medical devices, pharmaceuticals, cosmetics, or chemicals). **Technical Knowledge:** * Interpretation of **ISO 13485** and **NOM\-241\-SSA1**. * Good documentation practices. * Corrective, preventive, and improvement actions. * Proficiency with office tools (Word, Excel, PowerPoint). * Processing and control of statistical data. * Development of process mapping and document structure. * Quality standards and institutional policies. * Intermediate technical English (desirable). **Competencies:** * Commitment to work quality. * Attention to detail and organization. * Knowledge management. * Effective communication. * Teamwork. * Orientation toward internal and external customers. **What We Offer** * **100% statutory benefits.** * **5% savings fund.** * **Savings box.** * **Social benefits plan.** * **Subsidized cafeteria.** * **Professional training and development.** * **Stable and collaborative work environment.** * **Opportunities for growth within the company.** **Join MDC Dental** We are a leading Mexican company in the manufacturing of dental medical devices, committed to oral health and high-quality standards under international regulations. If you are passionate about quality, technical documentation, and continuous improvement, we invite you to join our team!