In this role, you will support commissioning, qualification, and validation activities for equipment, systems, and facilities in a regulated pharmaceutical environment. You will be responsible for preparing and executing validation documentation while ensuring compliance with cGMP standards. The position requires close collaboration with engineering and quality teams throughout the validation lifecycle.
Start Date: 15/03/2026
Duration: approx. 9 1/2 Months
Place of Work: Visp (full-time presence)
Key Responsibilities
* Coordinate installation and qualification activities for equipment and systems
* Prepare and review validation documentation such as URS, DQ, risk assessments, FAT, SAT, and validation protocols including IQ, OQ, and PQ
* Execute qualification protocols for equipment, systems, and utilities and ensure proper documentation of results according to cGMP standards
* Generate reports summarizing completed validation and qualification activities
* Contribute to the validation lifecycle including gap analysis, risk evaluation, and technical documentation
* Identify opportunities to improve efficiency within validation processes and apply lessons learned across projects
* Ensure validation activities remain aligned with current regulatory expectations and industry best practices
* Support quality system processes including document management, change control, deviations, and CAPA activities
* Develop and update procedures related to engineering and validation activities
* Collaborate with engineering teams to support validation strategies, requalification programs, and maintenance planning
* Perform additional project-related tasks as required
Candidate Profile
* Bachelor’s degree in a scientific or technical discipline
* Approximately five to ten years of experience within the pharmaceutical or regulated life sciences industry
* Strong knowledge of commissioning, qualification, and validation processes for equipment and facilities
* Experience working with validation lifecycle documentation and regulatory compliance requirements
* Excellent technical writing skills with the ability to create clear and accurate documentation
* Strong communication skills and the ability to collaborate effectively across departments
* Highly organized with strong time management capabilities
* Fluent in German and English
Job ID 18745
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