GMP Packaging Process Engineer — Automation & Yield

Sanofi; Waterford; On-site; EUR 50,000 - 70,000; Full time

Job summary

Sanofi Waterford is seeking a Process Engineer to support the Product Supply Unit’s inspection, device assembly, labeling, cartoning and packaging lines. You will contribute to reliable supply of syringe and vial products to patients worldwide.

The role emphasizes GMP compliance, technical problem solving, and collaboration with MSAT, Quality Assurance and Supply Chain to implement improvements and introduce new products and capacity.

Qualifications

• Experience in a highly regulated GMP environment.
• Degree in an Engineering discipline.
• Strong problem solving and communication skills.
• Strong documentation/protocol generation and execution skills.
• Automation experience is desirable.

Responsibilities

• Provide process engineering support to the Product Supply APU.
• Support delivery of continuous improvement projects to existing equipment.
• Work closely with MSAT, Technical Development, Quality Assurance, and Supply Chain.
• Lead and coordinate elements of projects and contribute to process engineering activities for new and existing capacity.
• Lead GPS initiatives including yield reviews, monitoring and optimisation.
• Apply knowledge from existing manufacturing technologies to develop new technologies for higher output and yield.
• Ensure safety compliance, provide technical support for failures, identify improvements and support qualification of new products/processes.
• Support new product introductions and capacity expansions, including vendor selections, maintenance planning, change controls, OEE and yield improvements.
• Lead systematic technical root cause investigations.
• Support safety and quality programs and initiatives.

Skills

GMP experience

Problem solving

Communication

Documentation

Automation experience

Education

Degree in Engineering

Job description

Sanofi Waterford is seeking a Process Engineer to support the Product Supply Unit’s inspection, device assembly, labeling, cartoning and packaging lines. You will contribute to reliable supply of syringe and vial products to patients worldwide.

The role emphasizes GMP compliance, technical problem solving, and collaboration with MSAT, Quality Assurance and Supply Chain to implement improvements and introduce new products and capacity.