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
An equal opportunity employer, Abbott welcomes and encourages diversity in our
workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
Thanks & Regards,
Satyabachan Acharjya
Technical Recruiter
INTELLECTT INC
Ext: 351
Direct: 7327905303
Email Me: acharya.s@intellectt.com