
Equipment Validation Specialist
- Ferentino, Frosinone
- Tempo indeterminato
- Full time
- Perform the analysis and evaluation of technical documentation for system to be qualified in order to acquire information necessary for the issue of protocols and the execution of activities.
- Issue of qualification protocols (IQ-OQ-PQ Protocols), through research and acquisition of data and information necessary to define their contents.
- Lead the external consultants in order to assure the correct qualification of the system/equipment (IQ-OQ-PQ Protocols).
- Carry out the analysis of the qualification activities and issue the qualification reports (IQ-OQ-PQ report), in compliance with current regulations (current EU GMP, US GMP) and company quality standards.
- Support the Quality Department in preparing Customer Audits and Regulatory Inspections, providing necessary information and documentation.
- Collaborate with other Site Departments in order to achieve the goal of the company’s projects.
- Participate in calls/meetings with customers/clients to support the discussion on topics related to equipment qualification.
- Collaborate with the Team Leader to close on time all assigned project.
- Technical / Scientific Degree (Mechanical Engineering, Chemical Engineering, CTF, Biomedical Engineering, Pharmacy, Industrial Chemistry).
- Experience in pharmaceutical industry.
- At least 2 years’ experience in Equipment Qualification Department.
- Knowledge of the main pharmaceutical machines/systems.
- Fluent in English.
- Good Team-worker.
- Good problem-solving abilities.
- Proficiency in Microsoft Office suite and electronic systems such as Documentum and Trackwise.
- Be prepared to work with conflicting priorities, under time constraints and in a dynamic team environment.