Manufacturing Systems Engineer – New Product Launches

Stryker Group; Cork; Hybrid; EUR 40,000 - 67,000; Full time

Benefits offered by this job

Benefits package

Job summary

Stryker Ireland is seeking an engineer to execute project elements for manufacturing systems and processes essential for bringing new products to market. You will support new product introductions, capital equipment qualification, and process validation, while ensuring GMP and safety compliance.

The role emphasizes strong cross-functional collaboration, detailed documentation, and adherence to regulatory requirements in a fast-paced environment.

Qualifications

• B.S. in Mechanical Engineering or related field.
• Ability to read complex drawings and GD&T.
• Experience in an FDA regulated or regulated industry beneficial.
• Strong communication and problem-solving skills.
• Enjoys fast-paced, results-oriented team environment.

Responsibilities

• Provide engineering support for new product and process introductions, ensuring activities are completed per NPD procedures.
• Project manage the introduction of new capital equipment and support qualification/validation activities.
• Evaluate process layouts for best floor space utilization and optimal process flow.
• Ensure quality of process and product per specifications.
• Participate in PFMEA, Control Plan, SOP and PPAP generation for product transfers and launches.
• Conduct MSA studies for new products and processes.
• Provide training for manufacturing team members.
• Ensure adherence to GMP and safety procedures.

Skills

Mechanical Eng. degree

Self-starter

Analytical skills

Cross-functional comms

GD&T reading

Regulatory experience

PC skills

Attention to detail

Education

B.S. in Mechanical Engineering

Tools

Draft reading tools

Job description

Stryker Ireland is seeking an engineer to execute project elements for manufacturing systems and processes essential for bringing new products to market. You will support new product introductions, capital equipment qualification, and process validation, while ensuring GMP and safety compliance.

The role emphasizes strong cross-functional collaboration, detailed documentation, and adherence to regulatory requirements in a fast-paced environment.