- 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

📌 Manufacturing Process Evaluation Specialist (Parets)
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📍 Parets