We are seeking a CSV Engineer for one of our client on a 6 to 12 months contract, in Geneva.
The ideal candidate will have a strong background in Computer System Validation (CSV) and Quality Assurance within the pharmaceutical and biotechnology industries. This role involves leading validation projects, managing IT infrastructure, and ensuring compliance with regulatory standards.
Key Responsibilities:
- Lead and manage CSV projects for IT and GMP operations applications and systems.
- Oversee the installation, configuration, and initial validation of SCADA-PLC software systems.
- Manage the rehosting of business applications and decommissioning & archiving projects.
- Provide lifecycle management support for business applications and industrial IT networks.
- Validate and integrate SCADA and MES systems, including hardware and software updates.
- Author and standardize procedures for CSV, data migration, and lifecycle management.
- Ensure continuous quality assurance of corporate systems and compliance with regulatory standards.
Qualifications:
- Bachelor's degree in Engineering, Computer Science, or a related field.
- 2 to 5 years of experience in CSV within the pharmaceutical or biotechnology industries.
- Experience in Quality Assurance within CSV a plus
- Proven track record of leading validation projects and managing IT infrastructure.
- Strong knowledge of SCADA, MES, and PLC systems.
- Excellent technical writing skills and experience authoring validation documentation.
- Familiarity with regulatory requirements and standards
- Excellent communication and interpersonal skills.
- Fluent French and English
For further information about this position please apply.
