Register Your Interest – Quality Opportunities

Sanmina; Fermoy; On-site; EUR 60,000 - 80,000; Full time

Job description

Overview

Due to exciting growth and strategic plans within Sanmina Fermoy, we currently have a number of exciting positions becoming available within our Quality Department. We are actively creating a talent pipeline and recruiting across the following areas for future vacancies:

• Quality Engineers
• Validation Engineers
• Supplier Quality Engineers
• Quality Technicians
• Quality Inspectors
• Document Controllers

About Sanmina Fermoy

Our Fermoy, Ireland, facility is FDA registered and certified to ISO 13485:2016 for the manufacture of high-quality PCBAs, subassemblies, and complete devices up to and including Class III medical devices.

Sanmina Fermoy’s core specialization is manufacturing automation. We provide services for the entire product lifecycle from New Product Introduction (NPI), prototyping, and process validation to complex volume manufacturing & test, shipping, and repair. We create a state-of-the-art environment for manufacturing medical and other high-quality devices. The facility has a track record of 30 years of outstanding operational performance and customer service, backed by a highly experienced workforce.

Why Join Sanmina?

• Make An Impact: Work on products that improve and save lives.
• Innovative Culture: Collaborate in diverse, cross-functional teams where ideas and improvements are encouraged and championed.
• Career Growth: Structured learning, internal mobility, and leadership opportunities help you reach your maximum potential.
• Core Values Matter: Honesty, integrity, transparency, personal accountability, and ethical business practices guide everything we do.
• Achieve Extraordinary Things: With the right tools, mindset, and support, you’ll thrive and make a tangible difference in the medical manufacturing field.

Who Thrives At Sanmina?

We are seeking professionals who align with our values and demonstrate the following core attributes:

• Learners & Problem-Solvers: Open to growth, curious, and willing to challenge the status quo to find the best solutions.
• Autonomous & Proactive: Able to take initiative, manage responsibilities, and make decisions independently when necessary.
• Collaborative Team Players: Teamwork and mutual support are fundamental to your approach.
• Committed & Engaged: Loyal to the business, deeply interested in the work, and dedicated to delivering excellent results.

General Candidate Requirements

While specific requirements vary by role, candidates should generally possess:

• Relevant third-level qualification (e.g., Degree, Diploma, or Certificate) in Engineering, Science, or a related discipline.
• Experience working within a regulated industry (e.g., Medical Device, Pharmaceutical) is highly desirable.
• Demonstrated knowledge of quality systems, validation protocols, or document control processes depending on the target role.

How To Register Your Interest

Please submit your most recent CV outlining your area of expertise (e.g., Validation Engineer or Quality Technician) and your relevant experience. Your details will be entered into our Quality Talent Pool. We will review your profile and contact you directly when a specific vacancy that matches your skills becomes available.