Validation Engineer - Automation & PLC

Pauwels Consulting; Wommelgem; Sur place; EUR 60 000 - 90 000; Plein temps

Résumé du poste

Pauwels Consulting seeks validation professionals to support automated pharmaceutical equipment across physical and simulated platforms in a strictly regulated environment. You will execute validation testing, ensure compliance with GAMP 5, 21 CFR Part 11, and GDP, and support control platforms such as SCADA (Siemens WinCC) and PLC (Siemens TIA Portal).

Willingness to travel worldwide, work in a flexible shift system, and thrive in complex technical settings are required; fluent English is

Qualifications

• 1+ to 5+ years of experience in pharmaceutical validation.
• Strong knowledge of SCADA/PLC control platforms.
• Thorough understanding of GAMP 5, 21 CFR Part 11 and GDP standards.

Responsabilités

• Execute validation testing for automated pharmaceutical equipment on physical machines and simulated bench systems.
• Ensure compliance with GAMP 5, 21 CFR Part 11 and GDP throughout the validation lifecycle.
• Support validation for SCADA/PLC platforms, including Siemens WinCC and Siemens TIA Portal.
• Perform on-site validation and equipment qualification at global customer locations.
• Maintain technical documentation and validation deliverables.

Connaissances

SCADA systems

Siemens WinCC

Siemens TIA Portal

PLC domains

GAMP 5

21 CFR Part 11

GDP

English

Travel readiness

Description du poste

Our client, a leading manufacturer of pharmaceutical production equipment, is seeking validation professionals to support their automated systems. The project focuses on testing complex machinery on both physical and simulated platforms within a strictly regulated environment.

• Execute validation testing for complex automated pharmaceutical equipment using physical machines and simulated bench systems.
• Ensure compliance with GAMP 5, 21 CFR Part 11, and GDP regulations throughout the validation lifecycle.
• Support validation efforts for control platforms including SCADA and PLC domains.
• Perform on-site validation and equipment qualification at various global customer locations.
• Maintain technical documentation and system knowledge to support high-quality validation deliverables.

• You bring 1+ to 5+ years of experience in pharmaceutical validation, depending on the seniority level.
• You have technical expertise in SCADA systems, specifically Siemens WinCC, and PLC domains including Siemens TIA Portal.
• You possess a thorough understanding of GAMP 5, 21 CFR Part 11, and GDP standards.
• You're willing to travel worldwide for international project execution and work in a flexible shift system.
• You're proactive, solution-oriented, and capable of rapid onboarding into complex technical environments.
• You are fluent in English.

Nice to Haves

• Experience with continuous manufacturing or tablet press equipment.
• Willingness to obtain additional certifications in automated system validation.