Project Engineer

Specialist in hiring engineers, pharmacists and business managers for Life Science in Switzerland !

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 support our clients in the realization of their projects on site by bringing your expertise and skills.

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

Responsibilities

• Lead the project for the design and implementation of a new cleanroom in a GMP environment, from feasibility studies to handover
• Prepare and manage project timelines, budgets, and resources, ensuring alignment with business objectives
• Coordinate design activities (layout, HVAC, utilities, equipment integration) with internal teams and external engineering partners
• Supervise procurement, installation, and qualification of cleanroom equipment, utilities, and infrastructure
• Ensure compliance of the project with GMP, ISO norms, and company quality standards
• Prepare and maintain technical documentation (URS, FDS, risk assessments, validation protocols, reports)
• Manage interactions with subcontractors, suppliers, and consultants, ensuring delivery according to specifications and quality standards
• Oversee commissioning, qualification, and validation activities (IQ/OQ/PQ) of the cleanroom and associated systems

Qualifications

• Engineering degree (mechanical, process, chemical, biotechnological, or related) or equivalent technical qualification
• Proven experience in cleanroom facility management in a GMP environment
• Strong project management skills, including planning, budgeting, and stakeholder coordination
• Knowledge of commissioning, qualification, and validation activities in a GMP context
• Familiarity with ISO, GMP, and relevant regulatory requirements
• Ability to work in a cross-functional, international environment
• Excellent communication and organizational skills
• English and German mandatory

Seniority level

Associate

Employment type

Full-time

Job function

Engineering, Project Management, and Consulting

Industries

Engineering Services, Pharmaceutical Manufacturing, and Biotechnology Research

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