Document Specialist - Intellectt : Job Details

Job Description:

• A minimum of a bachelor's degree in a Science/Engineering Mathematics, Computer Sciences or other relevant discipline

• A minimum of 1-3 years of overall experience in the medical device/pharmaceutical industry.

• Demonstrated knowledge of QSR/GMP (21 CFR Part 820) regulations and ISO (ISO 13485) standards is required.

• Knowledge of 21 CFR Part 11 and Computer/Quality System Software validation, preferred.

• Proficiency in training management and product lifecycle management (Agile) systems preferred.

Responsibilities:

• The position is responsible for facilitation quality system document control activities in compliance with U.S. and International requirements as defined in FDA Regulations, ISO Standards, European Medical Device Directives, and other International Regulations.

• Facilitates Document Change Orders for corporate quality system documents including document changes and training.

• Collaborates with document authors to release and implement of Global Standard Operating Procedures (GSOPs).

• Operate in Integra's corporate document control and training systems to transact changes to quality system documents.

• Support quality system training and management of quality system training requirements in LMS

• Execute change orders in alignment with quality system priorities and the global QMS Roadmap

• Participate to projects linked with corporate Doc Control activities.