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We are seeking a highly skilled Quality Assurance Manager to join our team at Medline, a global manufacturer and distributor of medical products with patient-centered solutions.
Key Responsibilities:
- Execute and coordinate Quality Engineering functions for the organization in sterile and non-sterile processes.
- Lead and coordinate Corrective and Preventive Actions (CAPA) for Customer complaints, and process non-conformities.
- Develop and define measurement equipment and test methods to evaluate and perform component or process 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).
- Serve as an ISO-13485 Lead Internal Auditor, participating in the Internal Audit Program.
- Ensure compliance with domestic and international regulations associated with product lines and processes.
To be successful in this role, you will need:
- Industrial, Electrical, etc 3-5 years of Quality Control/Engineering experience
- Medical Devices Experience (pharmaceutical, food or personal Care)
- Supervisory experience desirable
- Internal / Lead Auditor ISO 13485:2016
- MDSAP knowledge / experience
- Office Windows: Word, Excel, Power Point, etc.
- Strong leadership, effective communication, Management skills / Decision Making
- Six Sigma (BB/GB) Lean Manufacturing Experience
Medline is a global manufacturer and distributor of medical products with patient-centered solutions.
We are a leading company in the medical industry, with a strong commitment to quality and customer satisfaction.
We offer a dynamic and challenging work environment, with opportunities for professional growth and development.