Job Overview: We are seeking a highly skilled and experienced professional to join our team as a Validation Specialist. As a key member of our quality assurance department, you will play a critical role in ensuring the compliance and integrity of our computerized systems. The successful candidate will be responsible for validating computerized systems at site level, preparing validation documentation, performing periodic reviews, and ensuring proper execution of GxP activities. Additionally, you will establish maintenance and validation plans in collaboration with the quality department and manage system and plant infrastructure validation. This is an excellent opportunity for a motivated and detail-oriented individual to contribute to the development and implementation of quality control processes that meet industry standards. Responsibilities: Validate computerized systems at site level to ensure compliance with regulatory requirements Prepare and maintain validation documentation in accordance with current regulations and best practices Perform periodic reviews to maintain the validated status of computerized systems Evaluate and implement new technologies to improve efficiency and effectiveness of quality control processes Requirements: Degree in a relevant field such as sciences or engineering Minimum 1 year of experience in computer system validation and quality assurance Strong knowledge of GMP and CFR standards, their interpretation, and application Experience with EMA, FDA regulations, and pharmaceutical industry associations Fluent in English; additional languages are an asset Benefits: Competitive salary and benefits package Opportunities for professional growth and development A dynamic and supportive work environment Recognition and rewards for outstanding performance