Career opportunity software validation professional

Mid-Level Computer System Validation Engineer
Join a dynamic team of experts in Life Science Manufacturing Technology solutions to drive the growth and success of our business.
We are seeking a skilled CSV professional to support validation activities for GMP-regulated computerized systems across various environments.
This role focuses on hands-on execution of CSV lifecycle deliverables, working closely with Quality, Engineering, IT, and project teams to ensure compliance and timely delivery.Important Responsibilities
The ideal candidate will have hands-on experience validating GAMP Category 3 4 and 5 systems as well as executing validation protocols managing validation documentation.Solid understanding of CSV regulations quality expectations required.Good communication collaboration skills necessary.Leadership abilities desired.The following requirements must be met
1. Bachelor's degree in Engineering Life Sciences Computer Science or related discipline.
2. 4-7 years experience in Computer System Validation within a regulated pharma/biopharma environment.
This role offers opportunities for professional growth developmentCollaborate with local global CV teamsEnsure consistent executionEscalate potential issuesEHS site safety procedures during commissioning