AVI Engineer

RED Global; Italia; Remoto; EUR 60.000 - 90.000; Tempo pieno

Descrizione del lavoro

We are seeking an AVI Engineer (Automated Visual Inspection) to work on on-site projects across Italy, France, or Germany. The role focuses on automated inspection for vials, syringes, and parenteral products within a major pharmaceutical environment.

Start December 2026 on a 6-month contract. You will develop vision-based recipes, implement algorithms, and manage IQ/OQ/PQ tests while ensuring strict cGMP compliance and data integrity. Fluent English is required; local language is a bonus.

Competenze

• Bachelor's degree in Engineering (Mechanical, Electrical, Automation, Optical, Biomedical or similar).
• 7+ years’ hands-on experience in pharmaceutical/biopharma manufacturing, ideally with injectable products.
• Experience with AVI platforms and vision software.
• Solid understanding of cGMP, Annex1, USP guidelines and data integrity.
• English competence; local language a bonus.

Mansioni

• Develop and optimize automated visual inspection recipes for parenteral products.
• Work with vision algorithms and system integration to ensure product quality.
• Lead equipment qualification activities IQ/OQ/PQ and troubleshooting.
• Contribute to continuous improvement and regulatory compliance.

Conoscenze

AVI platforms experience

Vision software

cGMP knowledge

Regulatory compliance

English communication

Formazione

Bachelor's degree in Engineering

Strumenti

IQ/OQ/PQ

AVI systems

Descrizione del lavoro

AVI Engineer (Automated Visual Inspection) – Italy or France or Germany – On-site – 6-month contract – Start December2026

We’re looking for experienced AVI Engineers to join a major pharmaceutical company’s injectable manufacturing sites.

You’ll work on automated visual inspection systems for vials, syringes and other parenteral products, covering recipe development, vision algorithms, equipment qualification (IQ/OQ/PQ), troubleshooting and continuous improvement, all while maintaining strict cGMP and regulatory compliance.

What we’re looking for:

• Bachelor’s degree in Engineering (Mechanical, Electrical, Automation, Optical, Biomedical or similar)
• 7+ years’ hands‑on experience in pharmaceutical/biopharma manufacturing, ideally with injectable products
• Strong experience with AVI platforms and vision software
• Solid understanding of cGMP, Annex1, USP guidelines and data integrity
• Confident English (local language is a bonus)
• Right to work in the EU

If you enjoy the technical side of AVI and want to influence equipment decisions as well as execute them, this is a great opportunity.