Pharma Q&V Engineer: Packaging & Production

Pauwels Consulting; Eigenbrakel; On-site; EUR 55,000 - 75,000; Full time

Job summary

Pauwels Consulting is seeking a Qualification & Validation specialist to strengthen our manufacturing team in the pharmaceutical sector. The role focuses on supporting periodic qualification reviews and packaging equipment projects within a production environment.

You will execute qualification and validation activities for production and packaging equipment, manage validation tasks for combination products, and maintain thorough technical documentation.

Qualifications

• 3+ years of experience in Qualification & Validation within a pharmaceutical manufacturing environment.
• Experience in qualification of production and packaging equipment, specifically for combination products.
• Strong problem-solving skills and a proactive, autonomous mindset.
• Fluent in French with technical reading and writing proficiency in English.

Responsibilities

• Support the periodic review of qualification status for production and assembly systems.
• Execute qualification and validation activities for production and packaging equipment.
• Manage assembly and packaging validation tasks for combination products.
• Identify technical issues and propose appropriate solutions during the validation lifecycle.
• Prepare and execute qualification and validation protocols while maintaining technical documentation.
• Investigate deviations and technical issues related to equipment qualification.
• Collaborate with stakeholders to ensure timely execution and follow-up of assigned activities.

Skills

Qualification & Validation

Production equipment

Packaging equipment

Problem-solving

Autonomous mindset

French language

Tools

CSV (Computerized System Validation)

Job description

Pauwels Consulting is seeking a Qualification & Validation specialist to strengthen our manufacturing team in the pharmaceutical sector. The role focuses on supporting periodic qualification reviews and packaging equipment projects within a production environment.

You will execute qualification and validation activities for production and packaging equipment, manage validation tasks for combination products, and maintain thorough technical documentation.