Biotech Manufacturing Specialist - 24/7 Downstream Ops

1694 MSD Ireland (Dunboyne)

Dunboyne

On-site

EUR 42,000 - 64,000

Full time

11 days ago

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Benefits offered by this job

Hybrid working model

Job summary

MSD in Dunboyne is seeking a Manufacturing Biotech Associate to join our single-use Biologics Drug Substance facility. You will work in a self-directed team within Downstream Operations, manufacturing Drug Substance while upholding safety, quality, GMP, and compliance standards.

The role requires 24/7 shift operations (days, nights, rotation) and site-based work. You will develop deep downstream knowledge, collaborate across departments, and contribute to continuous improvement and documentation

Qualifications

  • A Level 7 or higher qualification in a science, engineering or technical discipline.
  • Experience in a GMP or regulated Cleanroom manufacturing environment.
  • Excellent communication skills and cross-functional collaboration.
  • Willingness to learn, adapt, and train others when proficient.
  • Knowledge of Upstream/Downstream processes, especially Downstream.
  • Proficiency with manufacturing systems and PC skills.

Responsibilities

  • Master complex processes in downstream bioprocessing.
  • Aim to be SME across Downstream; deepen micro-level knowledge.
  • Be approachable and supportive, fostering team cohesion.
  • Display flexibility and problem-solving to meet schedules.
  • Participate in inspections, GEMBA and Go-See initiatives.
  • Contribute to documentation and production system proficiency.

Skills

GMP Documentation
Good Manufacturing Practices (GMP)
Problem Solving
Lean Manufacturing
Kanban
Multidisciplinary Teamwork
Team Collaboration

Education

Science/Engineering degree (Level 7+)

Tools

MES
DeltaV
SAP
GLIMS
PROCAL

Job description

MSD in Dunboyne is seeking a Manufacturing Biotech Associate to join our single-use Biologics Drug Substance facility. You will work in a self-directed team within Downstream Operations, manufacturing Drug Substance while upholding safety, quality, GMP, and compliance standards.

The role requires 24/7 shift operations (days, nights, rotation) and site-based work. You will develop deep downstream knowledge, collaborate across departments, and contribute to continuous improvement and documentation

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