Manufacturing IT C&Q Engineer — GMP Compliance

Consultants in Science; Épalinges; On-site; CHF 90,000 - 120,000; Full time

Job summary

Consultants in Science is seeking an IT Manufacturing C&Q engineer for a global pharmaceutical company located near Neuchâtel, Switzerland. The role involves analyzing IT requirements, ensuring compliance with Good Manufacturing Practices, and managing multiple IT projects.

The ideal candidate should have 3–5 years of experience in the pharmaceutical industry, strong communication skills, and be fully operational in both French and English. Applicants must be eligible to work in Switzerland.

Qualifications

• 3–5 years’ experience as an IT engineer running projects from requirements to delivery.
• Experience with real-time data management and interfaces.
• Strong oral and written communication skills.

Responsibilities

• Analyze and document IT requirements and GMP regulations.
• Ensure data integrity of the system and its environment.
• Drive change management and training throughout the organization.

Skills

Experience in pharmaceutical or life science industry

Project management experience

Familiarity with change-management tools

Technical diploma in information systems

Fully operational in French and English

Education

Technical diploma in information systems

Tools

Kepware

Agile/Scrum

COTS

Job description

Consultants in Science is seeking an IT Manufacturing C&Q engineer for a global pharmaceutical company located near Neuchâtel, Switzerland. The role involves analyzing IT requirements, ensuring compliance with Good Manufacturing Practices, and managing multiple IT projects.

The ideal candidate should have 3–5 years of experience in the pharmaceutical industry, strong communication skills, and be fully operational in both French and English. Applicants must be eligible to work in Switzerland.