Quality Documentation Coordinator 4
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Job Location:
Monthly Salary:
Posted on:
4 days ago
Vacancies:
1 Vacancy
Job Summary
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 companys 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; Associates 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.
Required Experience:
IC
Key Skills
- Microsoft Access
- Quality Assurance
- Data Collection
- HEDIS
- ISO 9001
- Root cause Analysis
- Medical office experience
- Quality Systems
- Nursing
- Quality Control
- Quality Management
- Manufacturing
