- Control and document incidents arising in production and control processes- Supervise follow-up of corrective or preventive actions derived from incidents- Analyze process data and trends- Prepare system review reports based on collected and analyzed data- Coordinate follow-up groups to communicate process evaluations and trends- Review documentation describing production operations and equipment and facility functioning- Review qualification and validation protocols and reports- Prepare and deliver documentation requested during audits and inspections by national and international organizations and other companiesRequirements- Minimum education: Health Sciences Degree (Pharmacy, Biology,



Chemistry)- Master or Postgraduate degree in the pharmaceutical sector is valuable- Knowledge of GMP- Knowledge of Basic Statistics- Knowledge of MS Office and SAP- Advanced level of English- At least 2 years of experience in a similar position within QualityCore CompetenciesDemonstrates expertise in incident control, data analysis, and documentation within production processes, with a strong foundation in GMP and quality assurance practices. Proficient in preparing reports and coordinating communication for audits and inspections.Highest-signal resume keywords- Health Sciences Degree- Knowledge of GMP- Basic Statistics- MS Office- SAPHard Skills- Incident Control- Data Analysis- Documentation Preparation- Process Evaluation- Corrective Actions- Preventive Actions- Qualification Protocols- Validation Protocols- Quality Assurance- Audit PreparationSoft Skills- Communication- Supervision- CoordinationIndustry Keywords- Pharmaceutical Sector- Production Operations- Quality Control- International Standards- Inspection Compliance#J-18808-Ljbffr

📌 Manufacturing Process Evaluation Specialist (Barcelona)
🏢 Jobtailor
📍 Barcelona