Project Engineer

agap2 Switzerland; Basel; Presencial; CHF 110.000 - 140.000; Jornada completa

Descripción de la vacante

agap2 is seeking a Project Engineer to join as an on-site consultant in Basel, Switzerland, supporting pharma or chemical projects in GMP or ATEX environments. You will work from URS definition through commissioning supervision, interfacing with study, design, execution, and implementation stages.

You are expected to coordinate suppliers, site teams, and internal stakeholders to ensure successful project delivery and technical handover.

Formación

• Experience in GMP or ATEX environments within pharma or chemical industries.
• Willingness to manage the full project path from URS definition to commissioning supervision.
• Structured, collaborative approach to technical coordination and follow-up.

Responsabilidades

• Shape and review URS documents to align user needs, technical constraints, and project expectations.
• 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.

Conocimientos

GMP/ATEX experience

Project coordination

URS development

On-site work

Educación

Engineering degree in Pharma/Biotechnology or Chemical Engineering

Descripción del empleo

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