Validation Engineer; CQV

Execute commissioning, qualification, and validation activities for cutting-edge facilities. Provide expertise that guarantees safety, compliance, and operational readiness.

Type

Full-Time

Location

Compensation

CHF 95,000 – 115,000 per year

Employment Model

Permanent

As a Project Engineer at Vispact, you’ll manage projects from concept to completion, ensuring compliance with GMP and life science industry standards. You’ll collaborate with cross-functional teams to develop efficient solutions that meet quality and safety requirements.

You’ll play a key role in optimizing technical operations and ensuring that all engineering activities align with both regulatory and client expectations.

• Lead and manage engineering projects within GMP-regulated environments.
• Oversee design, commissioning, and qualification phases.
• Collaborate closely with quality, operations, and project teams.
• Ensure documentation and compliance with regulatory standards.
• Identify opportunities to optimize efficiency and reduce costs.

• Degree in Engineering, Life Sciences, or related field.
• 3–5 years of experience in project engineering, ideally in pharma or biotech.
• Knowledge of GMP, GAMP 5, and relevant EU/FDA guidelines.
• Strong communication and organizational skills.
• Fluent in English;
  German or French is a plus.

• Competitive compensation and transparent career growth.
• Hybrid or on-site flexibility (depending on role).
• Projects that directly impact global health and sustainability.

Submit your application, and our recruitment team will contact you if your experience aligns with our open opportunities.

Vispact Consulting delivers tailored engineering and management solutions for the life sciences industry. From project engineering to organizational transformation, we partner with you to drive sustainable growth and compliance.