QLTY & RELIABILITY TECHNICIAN III
Job Overview
What your background should look like:
SHIFT B: from Monday to Friday, 3:30 p.m. to 10:00 p.m and Saturdays from 7:00 a.m. to 2:00 p.m
KEY RESPONSIBILITIES& TASKS
- Maintain Quality Management System documentation files, verifying formats and revisions. Review changes to product configuration and manufacturing control process documentation.
- Timely distribution of the most current revision documentation to all users. Remove obsolete documentation at points of use and system.
- Receive and perform final review of Job Traveler’s process to ensure compliance with good documentation practices.
- Perform tasks as defined in document control procedures
- Create and follow up on NCMR's.
- Safeguard controlled documents including Drawings, Quality Manual, Standard Operating Procedures, work instructions, grinding process forms, Charts, job travelers, material specifications and others.
- Participate in tasks as assigned by the Quality Manager, related to the Quality Management System.
- May also support Internal Audits and Management Review processes.
- Must be able to support departments such as Doc Control, Training, Calibrations, Incoming, Environmental Monitoring, Pest Control and Methods.
SKILLS
- Language: Bilingual English (Intermediate)/ Spanish.
- Knowledge in Microsoft Office. Excel and Word intermediate mainly.
- Ability to communicate effectively orally and in writing.
- Ability to read and interpret changes in documents, such as, job travelers, sketches, diagrams, blueprints and other procedures.
- Proficient in geometry, fractions, percentages, ratios and measurements.
- Ability to gather relevant data, establish facts and find solution through actions. Problem solving.
- Effective time management/organization skills, applied in a pressured environment.
- Ability to work independently and in a team environment.
- Effective interpersonal skills and proficiency in interacting with culturally diverse employee population.
EXPERIENCE & EDUCATIONAL REQUIREMENTS
- +2 year of experience in a Quality Technician II position or Minimum 6 months internship in the medical industry in functions related to Quality. Quality leadership experience working in a manufacturing environment.
- High School Diploma.
- Certificate or Technical degree related to Quality (or with + 50 % of the technical degree completed.
- ISO 13485 auditor accreditation is desirable.
Competencies
San Rafael, A, CR, 20108
Job Segment:
Document Control, Facilities, Maintenance, QC, Administrative, Operations, Manufacturing, Bilingual, Quality