Similar Jobs

See all

Implementation Manager GxP

Benchling

US

GxP SaaS Agile

Director, IT Business Partner - Biopharma GXP

Nuvalent

US

Stakeholder Management Enterprise Architecture

Validation Engineer Responsibilities:

Execute Computer System Validation activities for Electronic Batch Record (EBR) systems.
Support development and review of validation deliverables, including URS, FDS, and risk assessments.
Participate in execution and documentation of validation testing (IQ, OQ, PQ).

Requirements:

Bachelor’s degree in Engineering, Computer Science, Life Sciences, or a related technical field.
3+ years of hands-on Computer System Validation (CSV) experience in a regulated pharmaceutical or biotechnology environment.
Working knowledge of cGMP regulations, including 21 CFR Part 11 and EU Annex 11.

Verista

Verista teams up with the world’s most recognizable brands in the life science industry to solve their business needs. They are a fast-paced organization with a people-focused culture.

Apply for This Position