Senior Bioprocess Operations Specialist – Dublin GMP

The Innopharma Group

Dublin

On-site

EUR 60,000 - 80,000

Full time

14 days+

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Job summary

Innopharma Group's Innopharma Technical Services in Dublin is seeking a Senior Manufacturing Bioprocess Associate to support a biopharmaceutical client site. The role focuses on GMP compliant manufacture of Drug Substance in a single-use facility.

You will operate and monitor process equipment, maintain cleanroom standards, troubleshoot issues, and contribute to continuous improvement. The position is site-based with shifts and requires willingness to work weekends or out-of-hours as needed.

Qualifications

  • Experience working in GMP manufacturing environments.
  • Ability to troubleshoot and resolve production issues.
  • Proven ability to work both independently and within cross-functional teams.

Responsibilities

  • Execute manufacturing operations in a GMP-compliant, sterile bioprocessing facility.
  • Develop and follow production schedules and batch records.
  • Operate in cleanroom environments and comply with SOPs and EBRs.
  • Support end-to-end production across Fed-Batch and Continuous Manufacturing.
  • Contribute to investigations and corrective actions.

Skills

Troubleshooting
Cross-functional teamwork
Independent work
Adaptability
Quality mindset

Education

Level 7 qualification in Science/Engineering
Level 6 qualification with 3+ years GMP experience

Tools

Emerson DeltaV
PAS-X
Single-use technology

Job description

Innopharma Group's Innopharma Technical Services in Dublin is seeking a Senior Manufacturing Bioprocess Associate to support a biopharmaceutical client site. The role focuses on GMP compliant manufacture of Drug Substance in a single-use facility.

You will operate and monitor process equipment, maintain cleanroom standards, troubleshoot issues, and contribute to continuous improvement. The position is site-based with shifts and requires willingness to work weekends or out-of-hours as needed.

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