CSV Engineer

Missions

Job Summary

As a CSV Engineer, you will be responsible for the Computerized Systems Validation (CSV) scope and collaboration with the Automation team. Your expertise in CSV, along with experience in large-scale projects and PLC/DeltaV systems, will contribute to the successful execution of projects in biopharmaceutical manufacturing facilities

Responsibilities

Lead the Computerized Systems Validation (CSV) process to ensure compliance with industry regulations and standards. Collaborate with the Automation team to integrate CSV activities within project timelines. Develop and execute validation protocols, test documentation, and CSV project deliverables. Liaise with departments, project managers, and vendors to coordinate CSV activities. Provide technical support to the Automation group during field execution and report writing. Generate and manage project change controls as required. Support Design Qualification efforts and participate in risk assessments. Adapt to changing project requirements and timelines. Maintain accurate documentation and records related to CSV activities. Missions Bachelor's degree in a relevant field (Engineering, Computer Science, etc.) is preferred. Minimum of 4/5 years of experience in CSV. Strong knowledge and experience with PLC and DeltaV systems. Experience working on large-scale projects. Preferred familiarity with design and construction projects in biopharmaceutical manufacturing facilities. Excellent communication and interpersonal skills. Strong problem-solving and analytical abilities. Ability to work effectively in a team environment.

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