Location: Switzerland (various project locations)

Company: Fortil Switzerland

Employment Type: Full-time

About Fortil
At Fortil, we believe in empowering engineers and consultants to lead impactful projects in life sciences, energy, and industrial sectors. With a presence across Europe, we are committed to innovation, excellence, and developing tailored solutions that advance our clients’ success.

Your Role
As a CQV/CSV Engineer, you will play a critical role in supporting commissioning, qualification, and validation activities for pharmaceutical manufacturing systems and equipment. You will ensure compliance with regulatory standards and drive the success of projects for our clients in Switzerland.

Your Responsibilities

- Lead and execute Commissioning, Qualification, and Validation (CQV) activities for GMP systems and processes

- Support and perform Computer System Validation (CSV) in compliance with GAMP and 21 CFR Part 11 requirements

- Draft, review, and execute validation protocols (IQ/OQ/PQ), risk assessments, and related documentation

- Coordinate with cross-functional teams including QA, Engineering, and Manufacturing

- Ensure project milestones are delivered on time and within regulatory expectations

- Participate in client meetings, audits, and inspections when necessary

Your Profile

- Minimum 5 years of experience in CQV/CSV roles

- Strong background in the pharmaceutical industry (GMP environment)

- Proven experience with equipment, utilities, and computerized systems validation

- Bilingual: fluent in English and French; German is a strong plus

- Excellent communication and organizational skills

- EU work permit or Swiss work authorization required

Why Join Fortil?

- Be part of a dynamic, international consultancy with ambitious growth

- Work on cutting-edge projects in the pharmaceutical sector

- Continuous learning and professional development opportunities