Downstream Bioprocess Specialist - 24/7 Manufacturing

Morgan McKinley

Leinster

On-site

EUR 65,000 - 90,000

Full time

2 days ago
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Job summary

Morgan McKinley is seeking a Specialist, Downstream Manufacturing (Downstream Bioprocess Associate) to support ongoing manufacturing operations and related commissioning/qualification activities in a 24/7 facility in Ireland. The role involves collaboration with CQV, Automation/CSV teams and production groups to ensure compliant, efficient operations.

The ideal candidate will have Level 6 engineering/science qualifications with 1–3+ years in a biopharmaceutical manufacturing setting, and

Qualifications

  • Bachelor-style level 6 or higher in Engineering/Science, or equivalent.
  • 1–3+ years in a large-scale biopharmaceutical manufacturing facility.
  • DeltaV and MES experience is advantageous.

Responsibilities

  • Support commissioning and qualification activities for process equipment.
  • Create operating procedures and documentation for large-scale manufacturing.
  • Execute manufacturing processes according to approved work instructions.
  • Adhere to cGMP and SOPs.
  • Participate in investigations and optimisations using science, engineering and lean principles.
  • Operate production equipment within the assigned area.
  • Utilise process automation systems (DeltaV, Syncade, OSI/Pi Historian) and business systems (SAP, Trackwise, Maximo).
  • Review batch and exception reports with Quality and input to investigations and QA audits.
  • Contribute to continuous improvement and operational excellence.

Skills

Communication
Problem solving
Independent worker
Cross-functional teamwork

Education

Level 6 qualification (Engineering/Science)

Tools

DeltaV
MES

Job description

Morgan McKinley is seeking a Specialist, Downstream Manufacturing (Downstream Bioprocess Associate) to support ongoing manufacturing operations and related commissioning/qualification activities in a 24/7 facility in Ireland. The role involves collaboration with CQV, Automation/CSV teams and production groups to ensure compliant, efficient operations.

The ideal candidate will have Level 6 engineering/science qualifications with 1–3+ years in a biopharmaceutical manufacturing setting, and

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