CSV Engineer

We are seeking a skilled CSV Engineer to join our team on a 6-month initial contract in Basel. The ideal candidate will have a robust background in Computer System Validation (CSV) and Automated systems within the pharmaceutical and biotechnology industries. This role involves leading validation projects and ensuring compliance with regulatory standards.

Key Responsibilities:

• Lead and manage CSV projects for IT and GMP operations applications and systems.
• Configure and initially validate software systems.
• Validate and integrate SCADA - PLC systems, including hardware and software updates.
• Author and standardize procedures for CSV, data migration, and lifecycle management.
• Conduct end-to-end data integrity assessments and standardize change management processes.
• Ensure continuous quality assurance of corporate systems and compliance with regulatory standards.

Qualifications:

• Bachelor's degree in Engineering, Computer Science, or a related field.
• 5+ years of experience in CSV within the pharmaceutical or biotechnology industries.
• Strong knowledge of SCADA and PLC systems.
• Experience in Quality Assurance within CSV is a plus.
• Proven track record of leading validation projects and managing IT infrastructure.
• Excellent technical writing skills and experience authoring validation documentation.
• Familiarity with regulatory requirements and standards.
• Excellent communication and interpersonal skills.
• Fluent in English.

Why Join Us:

• Work in Basel, a hub of innovation in the pharmaceutical industry.
• Competitive salary and benefits.
• Opportunity to work on cutting-edge projects.
• Collaborative and dynamic work environment.