Micro QC Analyst — Onsite Dublin (11-Month Contract)

Cpl Group

Dublin

On-site

EUR 42,000 - 56,000

Full time

9 days ago

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Job summary

Pfizer in partnership with Cpl Group seeks a QC Analyst Micro to join the team on an 11-month fixed-term contract at our Dublin plant in Grange Castle. This onsite role focuses on microbiology testing, calibration of instruments, and timely documentation in a cGMP environment.

The role requires a science/engineering background with strong communication skills; training will be provided and there are opportunities to support QA investigations and audits.

Qualifications

  • Requires degree: Science/Engineering or equivalent (not essential but preferred)
  • Excellent communication and interpersonal skills
  • Incumbents may be asked to perform other duties as required

Responsibilities

  • Perform microbiological testing on finished drug product, in-process materials, stability samples and environmental monitoring
  • Calibrate and use laboratory instrumentation
  • Document analytical results in a timely manner
  • Report non-conformances to the QC Manager
  • Assist in preparation/review of SOPs, reports, and protocols
  • Assist in training of other analysts and ensure training compliance
  • Support validation/qualification of test methods and processes
  • Facilitate investigations and support product investigations
  • Support laboratory inspections and audits
  • Troubleshoot lab methods and instrument issues
  • Maintain trend analysis programs and contribute to QC operations
  • Liaise with internal and external customers
  • Ensure samples analyzed meet batch disposition requirements

Skills

Excellent communication & Interperson

Education

Third level qualification in Science/Engineering or equivalent

Job description

Pfizer in partnership with Cpl Group seeks a QC Analyst Micro to join the team on an 11-month fixed-term contract at our Dublin plant in Grange Castle. This onsite role focuses on microbiology testing, calibration of instruments, and timely documentation in a cGMP environment.

The role requires a science/engineering background with strong communication skills; training will be provided and there are opportunities to support QA investigations and audits.

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