The position of Manufacturing LineQuality Engineer is within our Infectious Disease Developed Markets business unit located at Westbrook, Maine. In this role you will provide support for product quality assurance, process improvements and all quality system program at the Westbrook Site.
This job description will be reviewed periodically and is subject to change by management.
RESPONSIBILITIES:
· Support production with resolution of quality issues in accordance with established procedures.
· Support production on the manufacturing floor, ensuring adherence to procedures and ensure appropriate device history record (DHR) documentation. Supports line clearances, reworks, and inspections as required.
· Demonstrates commitment to the development, implementation and effectiveness of Quality Management System per ISO, FDA, and other regulatory agencies.
· Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
· Understands and is aware of the quality consequences which may occur from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities.
· Other duties as assigned, according to the changing needs of the business.
BASIC QUALIFICATIONS | EDUCATION:
· Bachelor's Degree in Engineering, Chemistry, Biotechnology, Life Science or other technical field or the equivalent combination of education and experience.
COMPETENCIES:
· Working knowledge of Database software; Internet software; Inventory software; Spreadsheet software and Word Processing software.
· Working knowledge of FDA, cGMPs/QSR and ISO quality system requirements
· Strong technical writing skills and effective communication skills
Job Type: Contract
Salary: $40.00 - $45.00 per hour
Expected hours: 40 per week
Benefits:
- Paid time off
Schedule:
- Monday to Friday
Experience:
- Manufacturing engineering: 3 years (Required)
- CAPA (Corrective Action and Preventive Action): 3 years (Required)
- GMP: 3 years (Required)
- ISO 13485: 1 year (Required)
Work Location: On the road