MedTech Process Engineer - GMP/Quality Improvement

jj; Limerick; On-site; EUR 55,000 - 90,000; Full time

Job summary

Johnson & Johnson’s Vision division seeks an Engineer to plan, execute, and deliver engineering activities in a GMP-regulated manufacturing setting. You will provide technical leadership to enhance safety, quality, delivery, and cost, while supporting IQ/OQ/PQ, change control, and CAPA processes in collaboration with Operations, Quality, and Supply Chain.

You will drive continuous improvement initiatives and work with cross-functional teams to ensure robust, scalable solutions that meet business

Qualifications

• Bachelor's degree in Engineering or related technical discipline.
• 2–4 years of relevant engineering experience in manufacturing or regulated environments.
• Demonstrated project execution experience.

Responsibilities

• Plan and execute engineering projects within a manufacturing value stream.
• Lead change control, validation (IQ/OQ/PQ), and CAPA support.
• Drive improvements in safety, quality, delivery and cost.
• Collaborate with Operations, Quality, Engineering, and Supply Chain.
• Ensure GMP/ISO/FDA compliance and continuous improvement.

Skills

Project execution

Cross-functional collaboration

Education

Bachelor's degree in Engineering or related technical discipline

Job description

Johnson & Johnson’s Vision division seeks an Engineer to plan, execute, and deliver engineering activities in a GMP-regulated manufacturing setting. You will provide technical leadership to enhance safety, quality, delivery, and cost, while supporting IQ/OQ/PQ, change control, and CAPA processes in collaboration with Operations, Quality, and Supply Chain.

You will drive continuous improvement initiatives and work with cross-functional teams to ensure robust, scalable solutions that meet business