
PACIV, Inc., with offices in Puerto Rico, Indiana, and Ireland, specializes in life sciences automation and regulatory compliance solutions. The company offers a range of services including control panel fabrication, system integration, and computer system validation to ensure consistent implementation across global manufacturing sites. PACIV's local presence and Master Service Agreements with leading Life Science companies underscore its commitment to quality and expertise, making it a key player in the industry.
PACIV is seeking an experienced CSV Engineer to support the validation and review of automation systems within a pharmaceutical manufacturing environment. The role involves developing validation documentation, testing, and preparing documentation, and collaborating with various functional groups. This is a site-based hybrid position requiring a valid EU Work Permit and Irish Residency.
PACIV, Inc., with offices in Puerto Rico, Indiana, and Ireland, specializes in life sciences automation and regulatory compliance solutions. The company offers a range of services including control panel fabrication, system integration, and computer system validation to ensure consistent implementation across global manufacturing sites. PACIV's local presence and Master Service Agreements with leading Life Science companies underscore its commitment to quality and expertise, making it a key player in the industry.