Project Engineer

agap2 Switzerland; Basel; Vor Ort; CHF 110.000 - 140.000; Vollzeit

Zusammenfassung

agap2 Switzerland in Basel is seeking a Project Engineer consultant to support pharma or chemical projects in GMP or ATEX environments, from URS definition through commissioning supervision.

You will coordinate study, design, execution and implementation stages, work on-site with suppliers, site teams and stakeholders, and ensure technical handover. The role requires a structured, collaborative approach to technical coordination across the full project path.

Qualifikationen

• Experience in GMP or ATEX environments in pharma or chemical industries.
• Comfort across URS definition to commissioning supervision.
• Structured, collaborative approach to technical coordination and follow-up.

Aufgaben

• Shape and review URS documents so that user needs, technical constraints, and project expectations are aligned early.
• Drive process and project engineering tasks across study, design, execution, and implementation stages.
• Coordinate suppliers, site teams, and internal stakeholders through commissioning supervision and technical handover.

Kenntnisse

GMP

ATEX

URS

Project coordination

Commissioning supervision

Ausbildung

Engineering degree in Pharma/Biotechnology or Chemical Engineering

Jobbeschreibung

agap2 is a European engineering and operational consulting group founded in 2005 and specialized in the industry. We work in the Pharma, Biotechnology, Medical Devices, Energy, Infrastructure, Transportation, Chemicals, and Information Technology sectors.

As a consultant, you will have to support our clients in the realization of their projects on site by bringing your expertise and your skills.

You are agile and eager to adapt to different work environments that will fuel your curiosity of seeing what’s behind closed doors of the biggest projects of our client’s portfolio.

This Project Engineer position sits at the interface of process engineering and project delivery. You will support pharma or chemical projects in GMP or ATEX environments, from the first URS definition through commissioning supervision.

What you will do

• Shape and review URS documents so that user needs, technical constraints, and project expectations are aligned early.
• Drive process and project engineering tasks across study, design, execution, and implementation stages.
• Coordinate suppliers, site teams, and internal stakeholders through commissioning supervision and technical handover.

What you bring

• Experience in GMP or ATEX environments in the pharma or chemical industries.
• Comfort working across the full project path, from URS definition to commissioning supervision.
• A structured, collaborative approach to technical coordination and follow-up.
• Engineering's degree in Pharma/Biotechnology or Chemical Engineering or a related field