Graduate Design Engineer — Biopharma Systems

Meissner; Ireland; Remote; EUR 35,000 - 45,000; Full time

Job summary

Meissner in Castlebar, Mayo, Ireland, invites applications for a Graduate Design Engineer. The role includes training at our HQ in Camarillo, California, to develop competencies for the position.

You will design, document and approve single-use systems primarily for the biopharmaceutical industry, providing support to end-users and collaborating with Quality, Operations, Engineering, Production, Sales and Supply Chain.

Qualifications

• Honours Bachelor degree in Mechanical Engineering or related technical discipline.
• Experience with AutoCAD and 3D modelling software.
• Ability to manage multiple projects concurrently.
• Strong analytical and mathematical skills.
• Excellent written and verbal communication in English.
• Experience in biopharmaceutical, pharmaceutical or manufacturing industries.

Responsibilities

• Develops single-use systems designs based on user and process requirements.
• Creates detailed specifications and URS responses for lean production.
• Prepares PFDs and BOMs for projects.
• Generates pricing with Global Finance and Accounting.
• Manages library of single-use components for assemblies.
• Evaluates components for fitness for purpose and tests performance.
• Supports production ensuring designs meet specs and improves MES/ERP usage.
• Provides pre- and post-sale technical support and creates usage diagrams.
• Manages projects to meet timelines and cost targets.

Skills

Multi-project management

Clear communication

Mathematical analysis

Biopharma experience

CAD/3D modelling

Education

Honours Bachelor degree in Mechanical Engineering

Bachelor-level degree in Biomedical/ Manufacturing Engineering

Tools

AutoCAD

3D Modelling Software

Job description

Meissner in Castlebar, Mayo, Ireland, invites applications for a Graduate Design Engineer. The role includes training at our HQ in Camarillo, California, to develop competencies for the position.

You will design, document and approve single-use systems primarily for the biopharmaceutical industry, providing support to end-users and collaborating with Quality, Operations, Engineering, Production, Sales and Supply Chain.