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 companies Requirements

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 Quality Core Competencies





Demonstrates 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 SAP Hard Skills

Incident Control Data Analysis Documentation Preparation Process Evaluation Corrective Actions Preventive Actions Qualification Protocols Validation Protocols Quality Assurance Audit Preparation Soft Skills

Communication Supervision Coordination Industry Keywords

Pharmaceutical Sector Production Operations Quality Control International Standards Inspection Compliance

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