- Disposition of non-conforming material (NCMR)
- Lead or participate in product complaint investigations to identify root causes
- Initiate and oversee Corrective Action and Preventive Actions (CAPA)
- Manage changes and associated documents according to standards and policies
- Conduct incoming part inspections (70% Mechanical, 30% Electrical)
- Perform in-process inspections
- High School diploma or GED
- 2-5 years of combined experience in Document Control, Inspection, and Quality Assurance
- Working knowledge of SAP PLM (1-2 years)
- Proficient in MS Word and Excel
- Strong organizational and detail-oriented skills
- Effective communication in a technical environment
- Customer-oriented team player
- No travel is required
- Prior experience in Medical Device/Biotech industry
- Experience with Document Control Platforms like Arena or Agile
- Ability to work semi-independently in a regulated environment
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Quality Engineer - Auburndale, United States - Viva USA, Inc.
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Description
Job Title: Quality Engineer - Onsite
Company: Leading Manufacturing Company
Description: Are you ready to join a dynamic team as a Quality Engineer? In this role, you will be responsible for ensuring the quality of products and processes. Take a closer look at the responsibilities and requirements below:
Required Knowledge/Skills, Education, and Experience:
Preferred Knowledge/Skills, Education, and Experience:
Notes:
Work hours: 9 am - 5 pm, with flexibility for core hours (8 am - 4 pm)