12 Month Contract to Start (Possibility of Extension)
A well-known Pharma company is looking to hire an experience Project Engineer at their Swiftwater, PA site. The role will primarily be onsite during executions, but there is some remote work flexibility. This individual will be responsible for designing, developing, approving and executing validation activities for pharmaceutical equipment and processes. This will include datapack compilation, data analysis, deviation resolution and report generation. Role responsibilities will additionally include the design, development, and approval of new or modified validation processes through coordinating agreements between stakeholders.
2-5+ Years of Relevant Experience required
Experience in temperature mapping would be ideal
Complex Technical Writing within a cGMP environment
Experience developing specifications, executing design reviews, performing criticality assessments, developing test scripts, executing common pharmaceutical tests, analyzing complex data packages and authoring complex technical reports.
Preferred: Experience with fermenters, bioreactors and the deltaV control system
Preferred: Experience developing and implementing novel processes and/or procedures in a cGMP environment
Sthree US is acting as an Employment Business in relation to this vacancy.