Project Engineer

Meet Life Sciences; Mirandola; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

Meet Life Sciences is seeking an experienced Process Engineer for a long-term freelance assignment in Mirandola, Italy. You will contribute to advanced manufacturing processes in a regulated environment within the medical devices sector, focusing on start-up, validation, and process improvement.

The role requires hands-on experience with FAT/SAT/OQ/PQ, statistical analysis (Minitab/DOE), and troubleshooting of plastics, moulding, and vision systems. Italian language proficiency is required.

Competenze

• Process engineering within a manufacturing environment
• Process start-up, industrialisation and validation
• FAT, SAT, OQ & PQ execution
• Writing and executing validation protocols
• Process improvement and manufacturing troubleshooting
• Root cause analysis and corrective actions
• Statistical process analysis including Minitab, DOE, CpK, PpK & Gage R&R
• Manufacturing technologies such as plastics, moulding, ultrasonic welding, bonding, leak testing or vision systems
• Experience within medical devices or another regulated manufacturing environment would be highly beneficial.

Conoscenze

Process engineering

Manufacturing start-up

Industrialisation

Validation protocols

FAT SAT OQ PQ

Root cause analysis

Statistical analysis

Moulding & plastics

Ultrasonic welding

Vision systems

Quality/regulatory environment

Descrizione del lavoro

Process Engineer - Mirandola, Italy

I'm currently supporting a leading medical device manufacturer who is looking for an experienced Process Engineer to join their manufacturing team on a long-term freelance contract.

The opportunity

• Location: Mirandola, Italy
• Contract: 15 months
• Start: ASAP
• Work pattern: Full-time, 5 days onsite
• Italian speaking required

We're looking for experience in:

• Process engineering within a manufacturing environment
• Process start-up, industrialisation and validation
• FAT, SAT, OQ & PQ execution
• Writing and executing validation protocols
• Process improvement and manufacturing troubleshooting
• Root cause analysis and corrective actions
• Statistical process analysis including Minitab, DOE, CpK, PpK & Gage R&R
• Manufacturing technologies such as plastics, moulding, ultrasonic welding, bonding, leak testing or vision systems

Experience within medical devices or another regulated manufacturing environment would be highly beneficial.