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Quality Technician

Req ID: J2314630

  • Ubicación
    Cayey, Puerto Rico, Puerto Rico, United States of America
  • Categoría Grupo de Calidad
  • Publicado lunes, 20 de junio de 2022
  • Tipo Tiempo completo
  • Tipo de Empleo Empleado Permanente

Descripción del Trabajo

Position Summary :

Verify the quality of the products against the customer specifications. Develops and maintains all Lot History Records.  Controls and issues all related Quality documentation.  Maintains documents and records within GMP regulation guidelines.

Observes company rules, regulations, and procedures, such as safety, housekeeping, attendance to educational activities and follows SOP’s and work instructions.

Key Responsibilities and End Results

  • Performs and documents inspection as the result of product quality plan, including cosmetic, functional, and dimensional inspection.
  • Identifies and segregate of non-conforming product to avoid mixes and errors.
  • Knowledge and management of audit.
  • Knowledge in material receipt inspections.
  • Responsible to control and release Product in Quality Hold.
  • Responsible for the reconciliation of labels and release of product in quality hold once the report these issues.
  • Performs startup and audits as required following Jabil documented procedures.
  • Responsible for the verbal and written report to the supervisor for each defect found in a product.
  • Authorizes to reject lots, accept conforming materials and to identify or segregate non-conforming materials and fill reports.
  • Verify the correct identification for the resin used, mold preventive maintenance status, operator inspection documentation and cleaning conditions in the molding operation.
  • Verify the correctness and neatness of documents and forms being to record inspections performed using Good Documentation Practices.
  • Maintains good communication with the next shift Technician, regarding any important issue that occurred in the machine, with the product, quality, etc.
  • Maintains retains samples and logs.
  • Observes all company rules, regulations, and procedures such as safety and housekeeping (6’s).
  • Expedites records and reports to customers.
  • Maintains all product Lot History Records
  • Maintains working area clean, organized, and safe.
  • Verify the accuracy of all records and reports.
  • Assures compliance to good documentation practices on history file (GMP).
  • Conduct audit of material at staging areas, process and / or parameters attributes if it is necessary or requested.
  • Complies with Good Manufacturing Practices.
  • Complies with all Manufacturing Procedures and Instruction applicable.
  • Follow rules that apply to clean room.
  • Responsible for the verbal and written report to the supervisor for each defect found in a product.
  • Responsible that his/her payroll clock punches are registered before entering or leaving, following, and accepting company payroll policies
  • Responsible of performing as per Job Description’s SOP’s and work instructions.
  • Attends all requested training or company meetings.
  • May participate in internal committees as Safety, improvement events, etc. as required.
  • Performs other responsibilities as assigned.

Education and Experience:

  • Associate Degree in Science related field preferred or minimum two year of College School plus two years’ experience in related Quality area.  One-year experience will be validated as one year of college education; if incumbent have basic knowledge of computer use and statistics. Fully Bilingual. PC Knowledge. Basic filing knowledge

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