Validation Technician

• Attractive salary, valued according to experience and professional career. Stable schedule from Monday to Friday, from 08:00 h to 17:00 h. Joining a consolidated and growing pharmaceutical company. Participation in high-impact technical projects with visibility within the organization. Collaborative and highly specialized environment. Continuous training and real opportunities for professional development. Job stability and a long-term growth plan. With us, talent has no labels. We firmly believe that talent has no gender, age, sexual orientation, origin, religion, or different abilities. Therefore, all our selection processes are based on the principles of transparency, objectivity, and equal opportunity.

Would you like to participate in the qualification of critical equipment and facilities within a highly regulated pharmaceutical plant? We are looking for a person with experience in GMP environments who wants to be part of key projects in validation, continuous improvement, and regulatory compliance.

• Execute qualification activities for equipment, facilities, and systems following applicable GMP standards. Prepare, review, and maintain technical documentation related to validation protocols, reports, and records. Manage periodic requalification programs for equipment and facilities. Evaluate the impact of technical changes in machinery and systems to determine the associated qualification requirements. Participate in risk analyses to define the scope and strategy of validation activities. Coordinate the commissioning and initial validation of new equipment together with the involved departments. Supervise activities related to critical systems such as HVAC, purified water, compressed air, and industrial gases. Provide support during regulatory audits and inspections, presenting the corresponding technical documentation.

• Education and experience University degree in Engineering, Pharmacy, Chemistry, or related disciplines. Between 5 and 10 years of experience in qualifications and validations within the pharmaceutical industry or highly regulated sectors. Demonstrable experience in the execution of IQ/OQ/PQ qualifications. Technical knowledge Solid knowledge of GMP, FDA, and EMA regulations. Experience in change management, risk analysis, and validation documentation. Valuable experience with critical plant systems and commissioning projects. Languages Technical English level for documentation management and participation in audits.