- 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

Antes de solicitar este puesto, por favor, lea la siguiente información sobre esta ocasión que encontrará a continuación.

- 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. xqbhyrx 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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