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