TRAINING SPECIALIST (BILINGUAL ENGLISH LEVEL) (H/M)

Gi Group es la multinacional Italiana líder en el mundo que ofrece soluciones integrales para el desarrollo del mercado laboral. Nuestra misión es contribuir con una visión global al desarrollo del mercado laboral con el objetivo principal de aumentar la empleabilidad, basándonos siempre en el valor personal y social del trabajo. Trabajamos día a día con nuestros candidatos y trabajadores para guiarles en su carrera profesional, y con nuestros clientes, para lograr un crecimiento y consecución de éxitos conjunta. Conoce más en https://es.gigroup.com/ HERE’S WHAT YOU’LL DO: Your key responsibilities will be: Overseeing the management of cGMP personnel qualification documents and training files within the electronic Document Management System (DMS). Collaborating with Subject Matter Experts (SMEs) to conduct Training Impact Assessments (TIAs) for new and revised documents, ensuring timely execution of related curricula and assignments. Maintaining compliance with GxP regulations, guidelines, and internal company policies to support global training standards. Executing all tasks precisely as defined by Standard Operating Procedures (SOPs) and work instructions, ensuring accuracy and consistency. Adhering to Good Documentation Practices (GDP) and Data Integrity requirements to maintain reliable training records, ensuring audit and inspection readiness. Your responsibilities will also include: Tracking, reporting, and maintaining training completion records for compliance with regulatory and internal timelines. Supporting LMS curricula modifications, assignments, and system-related updates. Ensuring timely completion of assigned training plans as per prescribed requalification cadence. Assisting in process improvements and optimizing training administration efficiency. Performing additional duties as assigned, supporting the ongoing needs of the Global GxP Training Program. EDUCATION: High School Diploma. Preferably a Bachelor’s degree in a scientific discipline EXPERIENCE : 1-3 Years experience in the biotechnology/biopharmaceutical industry, or other regulated industry. Preferably in Quality Assurance and/or Training / document control. 1 years administration experience in an eDMS and/or eLMS – preferably SuccessFactors / Plateau and/or Veeva CONDITIONS: Type of contract : Temporary (6 months). ETT Location : Madrid Modality : On-site Working hours : Full. 40 hours/week

Location: es, ES

Posted Date: 4/6/2025