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 forall 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 desirableBilingual 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 StandardsProficiency in: MS Office Suites and SAP.Works well in team setting as well as individually.Guide and develop documentation for team membersDesirable computer skills: AutoCAD, Solidworks, PDMworks, Visio.U.S.A Visa required.Availability to travel to the U.S. and other country if required.