Pharma Project Engineer – GMP Process Equipment

EFOR; Oberwallis; Vor Ort; CHF 90.000 - 130.000; Vollzeit

Zusammenfassung

EFOR Group, based in Visp, Switzerland, is seeking a TPL/Project Engineer to lead engineering design, development, and implementation of new or modified manufacturing systems for pharmaceutical environments. You will translate user requirements into technical solutions and coordinate multiple technical disciplines within the project.

The role requires 3-5 years in project engineering or management in (bio)chemical or pharmaceutical settings, with strong GMP awareness and proficiency in MS Office

Qualifikationen

• 3-5 years in project engineering or project management for (bio)chemical or pharmaceutical industries with international experience.
• Strong technical knowledge of engineering disciplines in the pharmaceutical environment.
• Experience with process equipment in pharma environments.
• Ability to work toward objectives and deliver results.
• Proficient MS Office tools (Word, Excel, PowerPoint, Visio).
• Experience working both independently and in teams is essential.

Aufgaben

• Review and approve engineering documentation and validation reports.
• Develop, check and approve P&IDs from status A to C, support adjustments to E.
• Support P&ID walkdowns and Mechanical Completion; manage punch lists.
• Ensure compliance with Lonza standards and GMP during engineering processes.
• Support commissioning and qualification of equipment and systems.
• Coordinate execution with external vendors, contractors, and suppliers.
• Act as liaison translating technical concepts to business implications.

Kenntnisse

Project engineering

English communication

German advantage

Team collaboration

Problem solving

Tools

Microsoft Word

Excel

PowerPoint

Visio

Jobbeschreibung

EFOR Group, based in Visp, Switzerland, is seeking a TPL/Project Engineer to lead engineering design, development, and implementation of new or modified manufacturing systems for pharmaceutical environments. You will translate user requirements into technical solutions and coordinate multiple technical disciplines within the project.

The role requires 3-5 years in project engineering or management in (bio)chemical or pharmaceutical settings, with strong GMP awareness and proficiency in MS Office