CSV Consultant - Remote

Overview

We are seeking a highly qualified CSV Consultant to join our team in Terrassa, Spain. As a CSV Consultant, you will play a crucial role in ensuring compliance and validation of computer systems within regulated industries, providing high-quality consulting services to our clients.

In Short

• Manage and execute assigned projects to meet client needs.
• Deliver qualification documentation that meets project and regulatory requirements.
• Ensure compliance with GxP regulations.
• Follow company policies on Quality, Environment, and Health and Safety.
• Collaborate effectively with various teams and clients.
• Conduct system audits and deficiency analysis.
• Adapt to changing priorities in a fast-paced environment.
• Travel as necessary for client commitments.
• Demonstrate strong project management skills.
• Possess a B2 level of English proficiency.

Requirements

• Technical degree in Computer Science, Electronics, Automation, or Life Sciences.
• 1-3 years of experience in system validation in the pharmaceutical industry.
• Deep knowledge of CSV-GMP guidelines and relevant regulatory requirements.
• Proficiency in CSV tools and industry-standard documentation practices.
• Excellent analytical and problem-solving skills with attention to detail.
• Strong communication and interpersonal skills.
• Experience in managing multiple projects simultaneously.
• Familiarity with quality management systems and documentation best practices.
• Driver's license and own vehicle.

Benefits

• Opportunity to work in a global company.
• Engagement in high-quality consulting services.
• Professional development opportunities.
• Collaborative work environment.
• Competitive compensation package.