Qualifications:
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:
The primary responsibility involves authoring, reviewing and implementing Computer System Validation deliverables needed to the deployment of IT system to a GMP environment. This role will leverage a deep understanding of Computer System Validation and Data Integrity principles ensuring compliance with regulatory requirements, consistent application, and sustainability for local and global IT systems used at the Concord Manufacturing site. This role will collaborate with the site organizations and global IT teams to enable best practices, processes, and governance and to consider new points to strengthen our CSV and Data Integrity position and align with corporate objectives and initiatives
Please take a moment to verify your personal information and resume are up-to-date before you apply.