We are looking for a professional with experience in qualification and validation of critical facilities and utilities in the pharmaceutical industry (HVAC, purified water, compressed air, electrical installations, etc.) to support one of our pharmaceutical clients in developing documented evidence compliant with appropriate requirements and specifications for their intended use and the current pharmaceutical regulatory framework. **RESPONSIBILITIES:** Preparation of qualification/validation master plans. Drafting of DQ / IQ / OQ / PQ protocols. Management and execution of equipment and system qualification activities. Process risk assessment and adherence to planning. Preparation of reports. **REQUIREMENTS:** Engineering degree or equivalent. Minimum 3 years of experience working in GMP environments and in equipment and process qualification within the facilities area (HVAC, electrical points, compressed air, etc.) in the pharmaceutical industry. Knowledge of GxP regulations, EMA, FDA, and CFR Part 11, as well as other systems, will be considered an advantage. High level of English: B2/C1 – spoken and written. Technical problem-solving skills and strong communication abilities. Rigorous and efficient individual, capable of collaborating effectively within multidisciplinary teams. **WHAT WE OFFER:** Joining a stable, high-impact project within the pharmaceutical sector. Participation in a GMP environment involving high-level technical validation and qualification projects. Integration into a specialized and growing team. High degree of autonomy and professional development. Permanent contract. Positive work environment and corporate culture. Flexible working hours. If you believe you meet the profile and are interested in this opportunity, please do not hesitate to apply. All criteria will be detailed further during the interview. We look forward to meeting you!
David Muñoz
Indeed · HR
David Muñoz
Indeed · HR
