Project Engineer at Visp

Project Engineer (m/f/d) – Pharmaceutical Industry

Valais Canton, Switzerland

Temporary contract - Immediate start until July 2027

We are currently supporting a leading pharmaceutical manufacturing site in Valais and are looking for an experienced Project Engineer to manage and deliver technical investment projects within a GMP-regulated environment.

Your Responsibilities

• Lead small to medium-sized engineering and capital investment projects from concept development through implementation and handover.
• Manage project scope, timelines, budgets, risks, and technical deliverables to ensure successful project execution.
• Conduct technical assessments and contribute to process and equipment improvement initiatives aimed at enhancing operational performance.
• Perform feasibility studies for new installations, facility upgrades, and process modifications.
• Develop and compare technical solutions, providing recommendations based on technical, operational, and financial considerations.
• Prepare project documentation, including cost estimates, schedules, technical specifications, and project justification packages.
• Coordinate internal stakeholders and external contractors to ensure project activities are delivered efficiently and according to plan.
• Monitor project progress and proactively address technical or scheduling challenges.
• Support manufacturing operations during equipment upgrades, process changes, and new product introductions.
• Collaborate closely with Engineering, Production, Maintenance, Quality, Validation, and HSE teams.
• Ensure all project activities comply with GMP requirements, company standards, and safety regulations.
• Drive effective communication across multidisciplinary teams and contribute to continuous improvement initiatives.

Your Profile

• Bachelor's or Master's degree in Mechanical Engineering, Process Engineering, Chemical Engineering, Biotechnology, or a related technical field.
• Minimum 5 years of experience managing engineering projects within a GMP-regulated pharmaceutical, biotech, or highly regulated industrial environment.
• Strong understanding of process engineering, manufacturing equipment, and facility systems.
• Experience managing CAPEX projects and coordinating multiple stakeholders.
• Ability to work independently while successfully operating within a matrix organization.
• Strong analytical and problem-solving skills with a structured and proactive approach.
• Excellent communication and interpersonal skills.
• Fluent English and German, both written and spoken.
• Solid business acumen with an understanding of project costs, budgeting, and operational impact.