Are you a Validation Engineer looking for your next contract opportunity in Denmark? Quanta has the role for you
Our client specialises in delivering pharma engineering solutions to the Danish pharmaceutical market. Contributing to over 1, engineering projects for their customers every year, they are experts in planning and establishing new pharma facilities, including upgrading, expanding, and supporting existing operations. As their impressive portfolio continues to grow, they are looking for a talented Validation Engineer to support the success of their latest large scale capital investment project.
Responsibilities: Part of the PQ team on a major expansion project Perform PQ activities of upstream process equipment Write, review, approve validation documents Execute testing, data evaluation and reporting Requirements: 3-5 years’ experience in performing and document qualification and validation 2-3 years of relevant industry experience from biological drug substance manufacturing Experience with PQ execution preferably from upstream equipment and steaming in place (SIP) testing Familiar with risk based Qualification and Kneat (Electronic Validation system) Hold a bachelor’s degree or higher in a relevant discipline If this role is of interest to you, please apply now
