Process Validation Engineer – Medtech Manufacturing

Enovis Corporation; Genova; On-site; EUR 45,000 - 65,000; Full time

Job summary

Enovis Corporation in Genoa, Liguria seeks a Process Validation Engineer for MedTech manufacturing. You will validate production equipment, systems, and processes and ensure compliance.

The role emphasizes documentation, cross-functional teamwork, and coordination with internal and external labs. English at B2 level and a proactive, detail-oriented approach are valued.

This position is based in Genoa, Italy and offers opportunities in a growing MedTech environment.

Qualifications

• 3–5 years in process validation.
• Strong teamwork and collaboration.
• English at B2 level.
• Proactive, detail-oriented with multi-tasking ability.

Responsibilities

• Validate production equipment, systems and processes.
• Coordinate with internal and external labs to ensure regulatory compliance.
• Maintain thorough validation documentation.
• Support quality and regulatory teams as needed.

Skills

Process validation

Teamwork

English (B2)

STEM background

Education

STEM degree

Job description

Enovis Corporation, Segesta (TP) in Sicily, seeks a Process Validation Engineer with a STEM background to qualify production equipment, systems, and processes.

Possiede le competenze, l'esperienza e la determinazione necessarie per avere successo in questo ruolo? Lo scopra qui sotto.

The role focuses on validation activities, documentation, and coordination with internal and external labs to ensure regulatory compliance. xlwpduy

Ideal candidates have 3–5 years in process validation, strong teamwork, and English at B2 level.

The position requires a proactive, detail-oriented approach and the ability to manage multiple

Process Validation Engineer – MedTech Manufacturing Genoa, Liguria, IT