Role: Quality Engineer
Location: Westbrook, ME
Duration: 06 Months on W2 (Possibility for extension)
Job Description
- Support production on the manufacturing floor, ensuring adherence to procedures and ensuring appropriate device history record (DHR) documentation.
- Support the NC and CAPA processes by completing risk assessments, root cause investigations, and action plans.
- Reviews qualifications, validations, and other studies for technical content, statistical and sampling rationale, unintended impact and clarity.
- May participate on design transfer and improvement project teams.
- Demonstrates commitment to the development, implementation and effectiveness of Quality Management System per ISO, FDA, and other regulatory agencies.
- May participate on design transfer and improvement project teams.
Basic Qualifications: Bachelor's Degree in Engineering, Chemistry, Biotechnology, Life
Preferred Qualifications: 2+ years' experience in the medical device or other regulated industry.
Competencies
- Knowledge of Agile programs.
- Working knowledge of Database software; Internet software; Spreadsheet software and Word Processing software.
- Working knowledge of FDA, CGMPs/QSR and ISO quality system requirements.
- Strong technical writing.