Bioprocess Associate: Inoculation & Cell Bank

WuXi Biologics; Leinster; On-site; EUR 36,000 - 48,000; Full time

Job summary

WuXi Biologics Dundalk is seeking an Inoculation and Cell-Bank Bioprocess Associate to support production of commercial Drug Substance. You will work with Manufacturing teams, follow SOPs, and help maintain cGMP-compliant operations.

The role requires 0–3 years in biopharma manufacturing, knowledge of aseptic technique and GMP, and experience with bioprocessing equipment, SAP, and TrackWise. You will train colleagues and contribute to continuous improvement while upholding safety and quality.

Qualifications

• Certificate, Diploma, Degree or equivalent in Science, Engineering or related field.
• 0–3 years’ experience in biopharmaceutical or pharmaceutical cGMP manufacturing.
• Experience in a greenfield context is an advantage.
• Strong knowledge of GMP and aseptic techniques.

Responsibilities

• Assist daily operations in the Inoculation and cell bank team.
• Maintain a safety-oriented, cGMP-compliant work environment.
• Support start-up and validation activities for facilities and equipment.
• Provide input on equipment installation, start-up, operation and troubleshooting.
• Contribute to achieving production output targets and quality on schedule.
• Record and follow SOPs, batch records, logbooks, and training.
• Identify improvement opportunities using Lean/Six Sigma tools.
• Notify supervisors of deviations and participate in investigations.
• Train and mentor colleagues in SOPs and equipment operation.
• Maintain high safety and regulatory standards.

Skills

Bioprocess knowledge

GMP knowledge

Aseptic technique

Problem solving

Education

Science/Engineering degree or equivalent

Tools

SAP

TrackWise

Process automation systems

Bioreactors

Centrifuges

Autoclaves

Job description

WuXi Biologics Dundalk is seeking an Inoculation and Cell-Bank Bioprocess Associate to support production of commercial Drug Substance. You will work with Manufacturing teams, follow SOPs, and help maintain cGMP-compliant operations.

The role requires 0–3 years in biopharma manufacturing, knowledge of aseptic technique and GMP, and experience with bioprocessing equipment, SAP, and TrackWise. You will train colleagues and contribute to continuous improvement while upholding safety and quality.