QC Microbiology Specialist

The Innopharma Group

Dublin

On-site

EUR 45,000 - 65,000

Full time

14 days+

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Job summary

Innopharma seeks a QC Microbiology Specialist to join its GMP manufacturing team in Dublin. You will support environmental monitoring, aseptic process qualification, and microbiological testing in a regulated environment.

Candidate with 2+ years in pharma/biotech labs and a Level 8 Microbiology degree will thrive in a proactive, cross-functional setting that values accuracy, teamwork, and continuous improvement.

Qualifications

  • Minimum Level 8 degree in Microbiology or a related discipline.
  • At least 2 years’ experience in a pharmaceutical, biotechnology, healthcare, or regulated laboratory environment.
  • Experience with environmental monitoring and aseptic processing concepts is preferred.

Responsibilities

  • Perform environmental monitoring of cleanrooms, BSCs, and isolators.
  • Carry out microbiological testing and analysis including in-process tests.
  • Support aseptic processing and APS/media fill activities.
  • Maintain accurate laboratory documentation and SOP compliance.
  • Collaborate with cross-functional teams to meet production timelines.

Skills

Environmental monitoring
Aseptic technique
Laboratory documentation
Communication

Education

Level 8 Microbiology degree

Tools

HPLC
UV Spectrophotometry
MODA
Empower
CIMS
LIMS
LES
Veeva Vault

Job description

We at Innopharma are seeking a highly motivated QC Microbiology Specialist to join our multinational client’s site based in Dublin and support their growing Quality Control team. As a QC Microbiology Specialist, you will support environmental monitoring, aseptic process qualification, and microbiological testing activities within a GMP-regulated manufacturing environment.

This is an excellent opportunity for a proactive microbiology professional to advance their career while contributing to the delivery of high-quality, safe, and compliant products.
Candidates must be willing to work shifts.

Key Responsibilities:

Environmental & Utility Monitoring

  • Performing cleanroom, Biological Safety Cabinet (BSC), and isolator batch-related monitoring.
  • Conducting utility sampling of water systems and Compressed Air/Gas.

Microbiological & Analytical Testing

  • Carrying out in-process testing, including HPLC and UV Spectrophotometry.
  • Issuing, receiving, and testing Biological Indicators (BIs).
  • Reading, reporting, and documenting results for environmental monitoring, BIs, and aseptic qualification samples.
  • Conducting microbial identification for isolates recovered during routine testing.

Aseptic Processing Support

  • Supporting media fill (APS) activities, including reconciliation and inspection of media fill units.
  • Ensuring compliance with SOPs, registered specifications, and GMP documentation standards.

Documentation

  • Completing laboratory documentation accurately and in a timely manner.
  • Assisting in the authoring and review of SOPs and technical documents.
  • Collaborating with cross-functional teams to meet qualification and production timelines.

Laboratory Standards

  • Maintaining a high level of housekeeping, safety, and aseptic discipline in the laboratory.
  • Supporting Lean lab and 6S initiatives to drive continuous improvement.
  • Performing additional tasks as assigned by the Microbiology Manager.
Preferred Experience:
  • Minimum Level 8 degree in Microbiology or a related discipline.
  • At least 2 years’ experience in a pharmaceutical, biotechnology, healthcare, or regulated laboratory environment.
  • Utility sampling of Compressed Air/Gas is essential.
  • Hands-on cleanroom and aseptic technique experience; isolator experience is a plus.
  • Isolator batch-related monitoring is essential.
  • Issuance, receipt, and testing of Biological Indicators is essential.
  • Reconciliation and inspection of media fill units, including participation in APS/media fills, is essential.
  • Desirable (not essential): experience with HPLC, UV Spectrophotometry, MODA, Empower, CIMS, LIMS, LES, or Veeva Vault.
  • Strong written and verbal communication skills.
  • A collaborative mindset and the ability to work effectively within a team.

Note:

  • All Applicants must be eligible to work in Ireland without VISA sponsorship.
  • All applicants must be willing to work in shifts.

INNOPHARMA, RAVENSCOURT BUSINESS PARK, THREE ROCK RD, SANDYFORD, DUBLIN 18, D18 K599, IRELAND

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