Manufacturing Engineer

CVI Infrared Optics; Shannon; Presencial; EUR 55.000 - 65.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Bonus potential

Descripción de la vacante

IDEX is hiring a Manufacturing Engineer to support and optimize Biopharma MUT and SUT pumping systems. You will act as the primary technical contact for manufacturing, focus on manufacturability, quality, and operational performance, and provide hands-on engineering support to production teams.

The role requires a Level 8 STEM degree, 4+ years in manufacturing, problem-solving skills, and experience with ERP systems.

Formación

• A minimum of Level 8 degree in a relevant STEM discipline.
• 4 Years experience supporting manufacturing operations within a technical or engineering environment.
• Experience in problem solving, root cause investigation, and continuous improvement methodologies.

Responsabilidades

• Provide hands-on engineering support to production teams to resolve assembly, testing, and product performance issues.
• Lead continuous improvement initiatives focused on safety, quality, cost reduction, waste elimination, and productivity enhancement.
• Collaborate with Design Engineering and R&D teams to improve product design and manufacturability.
• Support validation protocols and documentation for biopharma manufacturing equipment and processes.

Conocimientos

Problem solving

Root cause analysis

Lean manufacturing

Process optimization

Communication

Documentation

Educación

Level 8 STEM degree

4 years manufacturing experience

Herramientas

ERP systems

SolidWorks

Descripción del empleo

If you’re looking for a special place to build or grow your career, you’ve found it. Whether you’re an experienced professional, a recent college graduate or somewhere in between, IDEX is a place where you can apply your existing skills and learn new ones in an environment where you can make an impact.

With interesting opportunities in engineering, marketing, sales, supply chain, operations, HR, finance, and more across more than 40 diverse businesses around the globe, chances are, we have something special for you.

PRIMARY FUNCTION

The Manufacturing Engineer is responsible for supporting and optimizing the manufacture of Biopharma Multi-Use Technology (MUT) and Single-Use Technology (SUT) pumping systems and fluid management solutions. Acting as the primary technical support resource for manufacturing, the role is focused on improving product manufacturability, process efficiency, product quality, and operational performance. This role combines hands‑on manufacturing support with engineering expertise to ensure safe, compliant, and efficient production operations.

PRIMARY DUTIES AND RESPONSIBILITIES:

Manufacturing Engineering Support

• Serve as the primary technical point of contact for manufacturing issues relating to Biopharma product range of pump assemblies, and associated bioprocess equipment.
• Provide hands‑on engineering support to production teams to resolve assembly, testing, and product performance issues.
• Conduct root cause investigations and implement corrective actions to improve product quality, reliability, and manufacturing efficiency.
• Support day‑to‑day manufacturing activities, ensuring production targets, quality requirements, and customer commitments are achieved.

Process Development & Improvement

• Develop, implement, and maintain robust manufacturing processes for Biopharma pump systems.
• Lead continuous improvement initiatives focused on safety, quality, cost reduction, waste elimination, and productivity enhancement.
• Analyze production data and manufacturing metrics to identify trends, bottlenecks, and opportunities for improvement.
• Implement Lean Manufacturing, 5S, and process optimization initiatives to improve operational performance.

Product & Process Engineering

• Collaborate with Design Engineering and R&D teams to improve product design, manufacturability, serviceability, and product performance.
• Support engineering change implementation and product lifecycle management activities.
• Assist in the design and development of manufacturing fixtures, tooling, assembly aids, and test equipment.
• Support product validation, verification, and testing activities for new and existing products.

New Product Introduction (NPI)

• Lead manufacturing readiness activities for new products and product enhancements
• Develop assembly processes, standard work instructions, tooling requirements, and training plans to support successful product launches.
• Work closely with Production and Quality teams to ensure smooth transition from design to manufacturing.

Quality & Compliance

• Ensure manufacturing processes comply with good manufacturing practices, ISO, quality management systems, and applicable regulatory requirements.
• Support investigations of non‑conformances, customer complaints, CAPAs, and internal quality issues.
• Manage concession requests and deviation assessments in collaboration with Quality and Engineering teams.
• Support validation protocols and documentation associated with biopharma manufacturing equipment and processes.

Documentation & Technical Systems

• Create, review, and maintain manufacturing procedures, work instructions, process documentation, and standard work practices.
• Support ERP and manufacturing systems to ensure accurate product structures, routings, and manufacturing data are maintained.
• Maintain accurate engineering records and technical documentation in accordance with company standards.

Cross‑Functional Collaboration

• Work closely with Production, Quality Assurance, Supply Chain, Maintenance, and Engineering teams to support operational objectives.
• Support supplier quality improvement activities and technical evaluations where required.
• Provide technical training and guidance to production personnel on products, processes, and equipment.

Health, Safety & Environment

• Ensure engineering activities are conducted in accordance with company Health, Safety, Environmental, and Quality policies.
• Promote safe working practices and participate in risk assessments and safety improvement initiatives.
• Support compliance within controlled manufacturing environments where applicable.

Education & Experience

Essential

• A minimum of Level 8 degree in a relevant STEM discipline
• 4 Years experience supporting manufacturing operations within a technical or engineering environment.
• Experience in problem solving, root cause investigation, and continuous improvement methodologies.
• Ability to interpret engineering drawings, specifications, and manufacturing documentation.
• Experience using ERP systems and Microsoft Office applications.

Desirable

• Experience in biopharmaceutical, life sciences, medical device, or hygienic process equipment manufacturing.
• Knowledge of Multi‑Use Technology (MUT) and Single‑Use Technology (SUT) systems.
• Experience in GMP, FDA, and ISO quality requirements.
• Experience with SolidWorks or other 3D CAD software.
• Experience with validation, qualification, and testing processes within regulated industries.
• Working knowledge of pumps, fluid handling systems, rotating equipment, and process technologies.

Key Competencies

• Strong technical and analytical problem‑solving skills.
• Process improvement and Lean Manufacturing mindset.
• Effective project management and prioritization skills.
• Strong communication and stakeholder management abilities.
• Results focused with a proactive approach to problem solving.
• Excellent organizational and documentation skills.
• Ability to work effectively across engineering, production, and quality functions.

Organizational Relationships

The role works closely with:

• Production Operations
• Design Engineering & R&D
• Quality Assurance & Quality Control
• Supply Chain
• Maintenance & Facilities
• Customer Technical Support Teams

Compensation Information

The expected pay range for this position is 55,000 - 65,000 annually.

Ultimately, in determining your pay, we may also consider your experience, and other objective job‑related factors. This position may be eligible for a bonus or other incentive plan, as well as other forms of compensation.

Are you ready to join a different kind of company where our people, our culture, and our commitments are centered around providing trusted solutions that improve lives around the world?