Automation IOQ Engineer - AVEVA System Platform (Biopharma)

Nalys; Wallonië; On-site; EUR 60,000 - 90,000; Full time

Job summary

Nalys is seeking an Automation Qualification Engineer to join a major biopharmaceutical project. You will perform IOQ activities on the AVEVA System Platform/ArchestrA environment, ensuring strict GDP/ALCOA+ data integrity and compliant documentation.

You will work hands-on in a GMP setting, collaborating with automation, validation, and QA teams to drive execution and reporting, with a focus on timely delivery and reliability.

Qualifications

• Proven experience executing IOQ protocols in GMP environments.
• Hands-on knowledge of AVEVA System Platform / ArchestrA.
• Ability to retrieve configuration evidence from IDE and Galaxy.
• Familiarity with GAMP 5 and computerized system validation requirements.
• High level of documentation rigor and autonomy.
• Operational immediately in fast-paced project environments.
• Fluent in French and good command of technical English.
• Experience on a large biopharma production site is a strong asset.

Responsibilities

• Executing pre-approved IOQ protocols on the AVEVA System Platform / ArchestrA control system.
• Collecting test evidence directly in the system, covering configuration, HMI, alarms, historization, and security.
• Documenting results in line with GDP and ALCOA+ data integrity principles.
• Identifying, documenting and following up on deviations through to closure.
• Contributing to qualification reports and supporting the validation lifecycle.
• Working closely with automation, validation and QA stakeholders to keep the project on schedule.

Skills

IOQ execution

AVEVA ArchestrA

GAMP5 knowledge

Autonomy

Documentation rigor

English (technical)

French fluency

Tools

AVEVA System Platform

ArchestrA

Job description

Nalys is seeking an Automation Qualification Engineer to join a major biopharmaceutical project. You will perform IOQ activities on the AVEVA System Platform/ArchestrA environment, ensuring strict GDP/ALCOA+ data integrity and compliant documentation.

You will work hands-on in a GMP setting, collaborating with automation, validation, and QA teams to drive execution and reporting, with a focus on timely delivery and reliability.