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Job Description
A global pharmaceutical company seeks a Project Engineer to support site-based projects for Oral Solid Dose Manufacturing, Facilities, and Packaging operations.
Key Responsibilities:
- Support the Capital Projects Team with site-based projects.
- Execute validation support activities on site.
- Participate in continuous improvement programs, process mapping, and gap analysis.
- Optimize existing processes to achieve desired targets.
- Deliver projects and assigned duties on time and on budget.
- Coordinate changes using the approved change control procedure.
- Support validation activities for project activities.
- Design and write summaries for regulatory compliance or project-specific documentation.
- Update project details and lead project teams during scheduled project meetings.
Requirements:
- Bachelor's degree in Engineering.
- 5 years' experience in the Pharmaceutical Industry as a Project Engineer.
- Experience in cGMP, general packaging systems, and serialisation is advantageous.
- Ability to work and manage multiple departmental teams.
- Excellent technical writing ability.
- Strong documentation skills.
- Strong interpersonal and communication skills.
- Ability to work to the highest engineering standards.
- Strong technical and problem-solving skills.
- Willingness to travel within Europe.