Manufacturing Process Evaluation Specialist

• 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