Pharma Process Technologist — Solid Dose Expert

Takeda; Ireland; On-site; EUR 36,000 - 50,000; Full time

Benefits offered by this job

Healthcare cover

Pension

Bonus

Canteen

Parking with EV charging

Wellness programmes

Sports and Social club

Rewards scheme

Educational assistance

Job summary

Takeda at Grange Castle, Ireland, is seeking a P2 Plant Technologist to join the team and ensure manufacturing activities meet targets. You will follow all EHS and quality procedures, work onsite, and support problem solving from RCA to agile projects.

The role requires 5+ years in solid oral dose production, experience with MES/DCS, and a strong focus on safety, teamwork, and documentation. A competitive package and benefits are offered.

Qualifications

• Leaving Certificate or equivalent is required.
• 3rd level technical qualification in science or engineering is advantageous.
• 5+ years in Solid Oral Dose Production (encapsulation, tableting, dispense & blending, primary packaging).
• Experience with automated production systems (MES, DCS) desirable.
• Experience in high potent manufacturing is advantageous.
• Startup experience in pharma production is a plus.
• Knowledge of lean methodologies is desirable.
• Safety-focused with excellent teamwork, planning, documentation and PC skills.

Responsibilities

• Manage manufacturing operations in compliance with BMR/EBR and SOPs.
• Contribute to process improvements and validation under guidance.
• Ensure facilities operate at optimum efficiency and handle changeovers.
• Maintain housekeeping and safety standards; participate in site Emergency Response Team.
• Support training and assessment activities and ensure SOPs are read and recorded.

Skills

Teamwork

Planning

Documentation

PC skills

Safety focus

Education

Leaving Certificate or equivalent

3rd level technical qualification in science or engineering

Tools

MES

DCS

Job description

Takeda at Grange Castle, Ireland, is seeking a P2 Plant Technologist to join the team and ensure manufacturing activities meet targets. You will follow all EHS and quality procedures, work onsite, and support problem solving from RCA to agile projects.

The role requires 5+ years in solid oral dose production, experience with MES/DCS, and a strong focus on safety, teamwork, and documentation. A competitive package and benefits are offered.