Manufacturing Project Scientist Engineer

QCS Staffing Ltd; Dublin; On-site; EUR 50,000 - 70,000; Full time

Job summary

QCS Staffing Ltd in Dublin is seeking a Manufacturing Project Scientist Engineer for an initial 12-month contract in Life Sciences. You will work on major facility development and gain hands-on experience with innovative equipment and modern pharmaceutical technologies.

You will join cross-functional teams across manufacturing, engineering, QA, QC, regulatory, and supply chain to ensure compliant, efficient processes and smooth technology transitions.

Qualifications

• Currently completing a Bachelor's/Master's in Science, Engineering, or related subject.
• In-depth knowledge of GMP biologics manufacturing equipment and process automation.
• Strong working knowledge of DeltaV, MES Syncade and SAP.
• Excellent presentation skills.

Responsibilities

• Contributes to cross functional team (Manufacturing, Engineering, QA, QC, Regulatory, Supply Chain, etc.) for process improvement implementations, new product start-ups or other process changes at BMS
• Support new product introduction risk assessments to ensure the appropriate controls are in place to enable manufacturing
• Support product change over protocols to allow a smooth transition from sustaining to new product manufacturing
• Represent the Manufacturing at meeting to ensure the end user requirements are represented

Skills

GMP knowledge

DeltaV

MES Syncade

SAP

Presentation skills

Cross-functional collaboration

Education

Bachelor's/Master's in Science or Engineering

Tools

DeltaV

MES Syncade

SAP

Job description

Manufacturing Project Scientist Engineer – Ireland, Dublin – Initial 12-Month Contract – Life Sciences

Are you a Manufacturing Project Scientist Engineer looking for your next assignment in Dublin?

A leading multinational in Ireland’s thriving biopharma industry requires support for their major facility development.

This project provides hands‑on experience with innovative equipment, large‑scale operations and modern pharmaceutical technologies.

It’s an ideal opportunity to build your skills within one of Europe’s fastest‑growing life‑science regions.

What you’ll deliver:

• Contributes to cross functional team (Manufacturing, Engineering, QA, QC, Regulatory, Supply Chain, etc.) for process improvement implementations, new product start-ups or other process changes at BMS
• Support new product introduction risk assessments to ensure the appropriate controls are in place to enable manufacturing
• Support product change over protocols to allow a smooth transition from sustaining to new product manufacturing
• Represent the Manufacturing at meeting to ensure the end user requirements are represented

What you’ll need:

• Currently completing a Bachelors/Masters in Science, Engineering, or a related subject.
• In-depth theoretical knowledge of GMP biologics manufacturing equipment and process automation.
• Strong working knowledge of systems such as Delta V, MES Syncade and SAP.
• Excellent presentation skills.

Be part of something bigger.

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