Project Engineer
A leading pharmaceutical company is seeking a Project Engineer to support the development of oral solid dose manufacturing, facilities, and packaging operations.
The successful candidate will work closely with the Capital Projects Team to deliver projects on time and in accordance with cGMP regulations.
Key Responsibilities:
* Support site-based projects for Oral Solid Dose Manufacturing, Facilities, and Packaging operations
* Execute validation support activities on site
* Participate or lead continuous improvement programs, process mapping, and gap analysis
* Optimize existing processes to achieve desired targets
* Deliver projects and assigned duties on time and with high quality
* Coordinate changes using the approved change control procedure to ensure cGMP compliance
* Support validation activities for project activities, including reviewing validation documentation and attending validation activities
* Design and write summaries for regulatory compliance or project-specific documentation, including URS, DS, and detailed project schedules using MS Office applications
* Update project details regularly and lead project teams during scheduled project meetings, providing feedback and updates to team and senior management
Requirements:
* Bachelor's degree in Engineering
* 5 years' experience in the Pharmaceutical Industry as a Project Engineer
* Experience in cGMP, general packaging systems, and serialization is advantageous
* Ability and proven track record of working and managing multiple departmental teams for operational and capital projects
* Excellent technical writing ability
* Strong documentation skills
* Strong interpersonal and communication skills
* Must work to the highest engineering standards
* Have strong technical and problem-solving skills
* Willingsness to travel within Europe (minimal travel depending on projects)
This is a fantastic opportunity to join a dynamic team and contribute to the success of our company.