**Sr. Quality Document Coordinator** **Responsibilities:** + Under limited supervision, applies considerable Quality Systems knowledge to perform a broad range of tasks which include but are not limited to documentation and training staff on procedures. + Coordination of the approval, introduction, and modification of design, process, and quality documentation for + all products. + Ability to read, interpret, and apply the company’s quality policy and practices to ensure the documentation being processed, meets company standards. + Ability to read, analyze, and interpret technical drawings, procedures, and other various documents to ensure completeness and correctness. + Ability to use superior organizational skills, to efficiently get daily and routine tasks completed in a timely manner. + Ability to interact and communicate professionally with the documentation team. + Create and Maintain documentation. Facilitation of record monitoring, storage, and compliance with all departments. **Qualifications:** + High School Diploma required; Associate’s Degree desirable + Bilingual English/ Spanish (Excellent English communication skills) + 4 years’ related experience, preferably a medical device or pharmaceutical organization. + Working knowledge of ISO standards. + Familiar with Mechanical Drafting Standards + Proficiency in: MS Office Suites and SAP. + Works well in team setting as well as individually. + Guide and develop documentation for team members + Desirable computer skills: AutoCAD, Solidworks, PDMworks, Visio. + U.S.A Visa required. + Availability to travel to the U.S. and other country if required.