Project Engineer

agap2 Switzerland; Basel; Vor Ort; CHF 100.000 - 140.000; Vollzeit

Zusammenfassung

agap2 is a European engineering and operational consulting group. As a Project Engineer in Basel, you will support pharma or chemical projects in GMP or ATEX environments from URS definition through commissioning supervision, bridging process engineering and project delivery.

You will work on-site in Basel, coordinating suppliers, site teams, and internal stakeholders as projects progress through study, design, execution and implementation stages.

Qualifikationen

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

Aufgaben

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

Kenntnisse

URS docs

Process eng

Project coordination

GMP experience

ATEX environments

Ausbildung

Engineering degree in Pharma/Biotech or Chemical Eng

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