Senior QC Microbiologist - Impactful Pharma Quality Leader

PE Global; Leinster; On-site; EUR 65,000 - 101,000; Part time

Job summary

PE Global is recruiting a Senior QC Microbiologist for a leading multinational pharma client based in Dundalk. This is a contract position.

The Senior QC Micro Analyst works under the QC Manager/Associate Director to ensure compliance with cGMP and cGLP, data integrity, and reliable supply. Responsibilities include performing QC testing, reviewing data, contributing to OOS investigations, and maintaining QA documentation in a fast-paced biopharma environment.

Qualifications

• Degree qualification (Science/Quality/Technical or related)
• 4 years of laboratory experience, including sampling, testing, reporting in biotech/pharma
• 2-3 years of experience in QC Microbiology - knowledge of EM, Water Monitoring, Endotoxin Testing, Bioburden Testing
• Demonstrated commitment to learning and personal development
• Flexible and self-motivated; able to work on own initiative and in a team

Responsibilities

• Operate as part of the QC team performing allocated testing and lab duties.
• Act as testing SME with QC department; participate in OOS investigations and troubleshooting.
• Participate in QC Tier daily meetings; communicate testing progress and deviations.
• Assist in writing/revising/rolling out SOPs, training materials, and QA procedures.
• Peer review of testing documentation; ensure data integrity and QC KPI achievement.
• Support activities including audit readiness, equipment qualification, and method transfer/validation.

Skills

Problem solving

Communication

Time management

Teamwork

Self-motivation

Education

Science/Quality/Technical or related degree

Tools

Microsoft Office

Job description

PE Global is recruiting a Senior QC Microbiologist for a leading multinational pharma client based in Dundalk. This is a contract position.

The Senior QC Micro Analyst works under the QC Manager/Associate Director to ensure compliance with cGMP and cGLP, data integrity, and reliable supply. Responsibilities include performing QC testing, reviewing data, contributing to OOS investigations, and maintaining QA documentation in a fast-paced biopharma environment.