Biotech Manufacturing Associate (24/7 Shift) – Hybrid

Merck

Ireland

On-site

EUR 40,000 - 70,000

Full time

4 days ago
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Benefits offered by this job

Hybrid working model

Job summary

Merck's Dunboyne site seeks a Manufacturing Biotech Associate to join the Downstream Operations team. The role focuses on Drug Substance manufacture within a single‑use facility, maintaining high safety, quality, GMP and compliance standards.

The position requires flexibility to work 24/7 shifts and is site‑based. You will collaborate cross‑functionally to grasp processes at a micro level, contribute to process improvements, and support production goals while upholding a culture of teamwork and

Qualifications

  • A Level 7 or higher qualification in science, engineering or technical discipline.
  • Experience in GMP or regulated Cleanroom manufacturing is advantageous.
  • Excellent communication and cross-functional collaboration skills.
  • Willingness to learn, adapt and train others to proficiency.
  • Knowledge of Upstream/Downstream processes, especially Downstream processes.

Responsibilities

  • Operate within a self‑directed team to manufacture Drug Substance.
  • Uphold Safety, Quality, GMP and Right First Time standards.
  • Participate in 24/7 shift operations including days, nights, and rotations.
  • Deliver shift handovers, Tier meetings and issue resolutions promptly.
  • Collaborate with departments to meet production schedules and business unit goals.
  • Engage in inspections, GEMBA walks, improvements and Go‑See activities.

Skills

GMP standards
Cross-functional teamwork
Problem solving
Communication skills
Shift work flexibility
Lean manufacturing
Downstream knowledge

Education

Level 7 or higher in science/engineering/technical discipline

Tools

MES
DeltaV
SAP
GLIMS
PROCAL

Job description

Merck's Dunboyne site seeks a Manufacturing Biotech Associate to join the Downstream Operations team. The role focuses on Drug Substance manufacture within a single‑use facility, maintaining high safety, quality, GMP and compliance standards.

The position requires flexibility to work 24/7 shifts and is site‑based. You will collaborate cross‑functionally to grasp processes at a micro level, contribute to process improvements, and support production goals while upholding a culture of teamwork and

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