Global Computer System Validation Manager

Are you ready to join a leading global consulting company in the pharmaceutical and Medical Device industry? PQE Group has been established in this sector since 1998, ensuring an international presence thanks to its 45 subsidiaries and 2,000 employees in Europe, Asia, and the Americas. Working for a consulting reality like PQE Group will give you: The opportunity to work on projects for the most important national and international pharmaceutical companies, acquiring transversal skills and expertise. You will be part of a dynamic team that supports clients in the development and implementation of computerized systems, ensuring compliance with regulatory requirements and industry standards. Your role will involve: Developing and implementing validation plans and protocols; Conducting risk assessments and identifying potential issues; Collaborating with cross-functional teams to ensure effective communication and coordination; Providing training and support to clients on computer system validation best practices; Staying up-to-date with the latest regulatory requirements and industry trends. If you are a motivated and organized individual with a passion for technology and consulting, we want to hear from you! PQE Group offers: A dynamic and international work environment; Opportunities for professional growth and development; Competitive salary and benefits package; Flexible working hours and remote work options.