Ingeniero Sr. Calidad
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Requirements
- Bachelor's degree in Engineering or business-related field preferred.
- At least 3 - 5 years of quality control related work required.
- Preferably in a regulated industry (Medical Device, Pharmaceutical, Food or Personal Care).
- Supervisory experience preferred but not mandatory.
- Intermediate level skill in Microsoft Excel and Word
- Six-Sigma Black Belt of Green Belt
- Knowledge in Lean Manufacturing concepts
- Strong written and verbal English and Spanish skills.
- Strong leadership skills
- Effective communication
- Self-iniative
- Excellent attention to detail and time managment skills
- Ability to critically think about situations and independently make decisions.
- Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, disability/handicap status or any other legally protected characteristic.
Additional Information
Job Description General Objective: This position executes and coordinates Quality Engineering functions for the organization. The position requires a dynamic, hard-working quality professional with a desire to work for a fast-paced, large corporate organization. In addition to exceptional communication skills, a "roll-up" your sleeves" entrepreneurial attitude is expected. Responsabilities: Lead and coordinate Corrective and Preventive Actions (CAPA) for Customer complaints, and process non-conformities. Communicate product quality issues, data analysis, trends, and/or other information to respective internal customers. Continual process reviews through the use of the defined process failure mode analysis (PFMEAs) documents. Develop processes and plans to identify trends and focus on customer complaints, and in-process non-conformances. Develop and define measurement equipment to evaluate and perform component inspections. Define effective control plans for warehouse to operations delivery of raw materials' processes. Define, and lead continuous improvement projects focused on quality improvement, and cost reductions. Perform periodic audits of the accuracy and cleanliness of component storage locations and communicate results with appropriate warehouse personnel. Support the implementation and improvements for Good Manufacturing Practices (GMPs).
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