QC Analyst Job at Eurofins, Ireland | Apply Online | Biotechnology Client Site
Interested in laboratory testing that supports quality in biotechnology manufacturing? This Eurofins QC Analyst Job at PSS Insourcing Solutions involves water analysis, laboratory sampling and GMP documentation at a leading biotechnology client site. Based in Shanbally Cross, Ireland, the position is a 12-month fixed-term contract for candidates with relevant scientific qualifications and regulated laboratory experience.
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Job Position: QC Analyst
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Location: Shanbally Cross, Ireland
About The Company
Eurofins Scientific provides analytical testing services across multiple industries. Its PSS Insourcing Solutions business places specialist teams directly at client sites, where they use client facilities, equipment and methods while working within Eurofins’ cGMP compliance framework.
QC Analyst Job: Role Overview
In this Eurofins QC Analyst Job, the analyst will join a cross-functional team supporting the Bioassay Quality Control testing function. Activities include water testing, environmental monitoring-related experience, analytical data review and daily laboratory support.
The role requires accurate documentation, sound cGMP knowledge and the ability to respond to changing priorities while maintaining quality and safety standards.
Key Responsibilities
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Perform water analyses, including appearance, nitrates, Total Organic Carbon (TOC) and conductivity testing.
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Carry out laboratory sampling according to GMP and quality requirements.
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Review analytical data and support deviation investigations and problem-solving.
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Assist with protocols, reports, SOPs and other laboratory documentation.
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Complete equipment checks, housekeeping, inventory management and waste disposal.
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Communicate progress to client teams and colleagues.
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Maintain training records and train team members where appropriate.
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Contribute to continuous improvement and provide team cover as needed.
Education and Experience
Applicants must have:
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A degree in Microbiology or a related scientific discipline.
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At least one year of experience in a pharmaceutical or regulated GMP environment.
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A sound understanding of current Good Manufacturing Practice (cGMP).
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Academic and/or practical Environmental Monitoring (EM) experience.
Skills Required
Candidates should demonstrate strong written and verbal communication, accurate documentation and a customer-focused approach. Organization, attention to detail and self-motivation are important, alongside the ability to work independently and collaboratively.
The position also requires flexibility, effective prioritization and the ability to meet timelines in a fast-paced environment.
For scientists with GMP experience who enjoy precise testing and collaborative laboratory work, this Eurofins QC Analyst Job offers the opportunity to support biotechnology quality control. Bring your analytical skills, documentation discipline and commitment to reliable results to Eurofins’ client-site team.

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