Descripción del Empleo:
Position Responsibilities • Drives and facilitates the timely change, approval and release of documentation according to project schedules, including the resolution of resource issues relative to the creation (e.g. word processing work).
• Performs all aspects of complex engineering changes, including ECO/ Change Action (CA) processing, parts lists (BOM’s) changes, ERP input, manufacturing processes and general document verification.
• Monitors configuration and documents changes management process effectiveness including the impact of changes and takes the initiative to recommend configuration and change management process improvements.
• Assists in the implementation and maintenance of documentation and configuration assurance processes for the control of review, revision, distribution, production, retrieval of records associated with device master records, design history records
Requisitos:
Minimum Education Bachelor Degree Basic Qualifications Background • Educational: Science, Engineering, Business Administration or related field
• Experience:
o Associate or Level 1: 0 Years with Diploma/ Degree
o Intermediate or Level 2: 3+ Years with Diploma/ Degree or 0 Years with Advanced Diploma/ Degree
o Senior or Level 3 5+ Years with Diploma/ Degree or 3+ Years with Advanced Diploma/ Degree
o Principal or Level 4: 7+ Years with Diploma/ Degree or 5+ Years with Advanced Diploma/ Degree
o Senior Principal or Consultant or Level 5: 10+ Years with Diploma/ Degree or 7+ Years with Advanced Diploma/ Degree
• Exposure to quality and manufacturing environment
Skills
• Interpersonal Relations
• Quality and Results Oriented
• Computer Literate
• Fluency speaking and writing in English and Spanish
Desired/ Preferred
Qualifications Background
• Experience in medical dev