Senior Manufacturing Engineer - Galway
Our client is a fast-growing medical technology company on a mission to transform how patients experience cancer treatment.
They design and build breakthrough technologies that enable healthcare providers to deliver care that is more effective, accessible, and cost-efficient.
As the company approaches key milestones in product development and commercialization, they are seeking a
Senior Manufacturing Engineer
to lead manufacturing and process development for their latest device—a pioneering technology that enables cancer care in the home.
This role offers the opportunity to be part of a rapidly scaling organization, working at the intersection of R&D, Quality, Design Assurance, and Operations to bring life-changing technologies to patients.
Why Join This Client?
Impactful Work:
Contribute to the development and delivery of high-impact medical devices that make a real difference to patients.
Growth Opportunities:
Comprehensive training and continuous personal and professional development are embedded in the company's culture.
Flexibility and Benefits:
A competitive salary, strong benefits package, flexible working hours, and a generous vacation policy are all part of the offer.
Early Influence:
As a key hire, you will have the chance to shape manufacturing processes and influence the growth trajectory of an innovative start-up.
Key Responsibilities
Collaborate with R&D on optimizing product designs for manufacturability (DFM) and assembly (DFA).
Establish and validate a new assembly line within a Class 8 cleanroom, including jig and fixture design.
Lead equipment and process validation for device assembly.
Support builds for R&D testing, product verification, validation, clinical trials, and commercial launch.
Develop robust work instructions, test methods, and process controls.
Drive root cause investigations and resolve process non-conformances.
Manage timelines for manufacturing projects and coordinate with external suppliers.
Continuously identify and implement manufacturing process improvements.
Utilize CAD tools and in-house prototyping equipment to design and refine fixtures.
Ensure delivery of projects on time, on cost, and to quality standards.
Candidate Profile
The ideal candidate will be:
Creative
– a resourceful problem solver with a passion for innovation.
Open
– collaborative, positive, and receptive to constructive feedback.
Communicative
– skilled in written and verbal communication across teams.
Self-Driven
– proactive, accountable, and motivated to take ownership.
Organised
– capable of managing priorities and meeting deadlines.
Team-Oriented
– thrives in multidisciplinary, mission-driven environments.
Experience Required
Degree in Engineering or a related technical discipline.
6+ years of relevant experience in a manufacturing environment, with at least 3 years in the medical device industry.
Proven expertise in:
ISO13485 or equivalent quality management systems.
Cleanroom assembly and polymer processing.
Process and equipment validation.
Root cause investigations and process optimization.
Managing external suppliers.
Additional Advantages
Advanced qualification (Masters or Diploma) in a technical field.
Experience with PCBs and/or electromechanical components.
Cleanroom design and assembly line configuration.
Previous start-up or SME experience.
Prototyping experience (3D printing, vacuum forming, heat sealing).
Supplier process validation (e.g., injection moulding).
Leadership in line installations, transfers, or new process development.
Familiarity with Lean manufacturing tools and methods.
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