GMP IT System Validation Specialist - Raleigh, United States - Global Channel Management

Description

Qualifications And Experience

Bachelor's degree in Software Engineering, Computer Science, Computer Engineering, or a related field.
Minimum of 5+ years of experience working with Computer System Validations in a GMP pharmaceutical environment.

Responsibilities As An IT CSV Analyst

Authoring, Reviewing, and

Implementing Validation Deliverables:

As an IT CSV Analyst, you will be responsible for authoring, reviewing, and implementing Computer System Validation deliverables necessary for deploying IT systems in a GMP environment.

Ensuring Compliance And Data Integrity

Utilize a comprehensive understanding of Computer System Validation and Data Integrity principles to ensure compliance with regulatory requirements. This includes ensuring consistent application and sustainability of IT systems used locally and globally at the Manufacturing site.

Collaboration And Best Practices

Collaborating with site organizations and global IT teams is a key aspect of the role. This collaboration aims to establish best practices, processes, and governance.

By considering new approaches, the goal is to enhance the CSV and Data Integrity position, aligning with corporate objectives and initiatives.

Employment Type:
Full-Time

#J-18808-Ljbffr