QC Raw Materials Analyst

Morgan McKinley; Ireland; On-site; EUR 55,000 - 70,000; Full time

Job summary

Morgan McKinley is seeking a QC Raw Materials Specialist for a state-of-the-art biologics manufacturing facility in Dublin. You will perform routine QC testing of water samples and raw materials, using techniques such as HPLC, KF, UV, and IR, while maintaining strict documentation and compliance with cGMP standards.

Reporting to the QC Raw Materials Manager, you will help ensure data integrity, support technical transfers, and contribute to continuous improvement initiatives within a regulated

Qualifications

• A minimum of a third-level degree in Chemistry, Biology, or a related scientific discipline.
• At least 2–3 years of experience in a pharmaceutical/biopharmaceutical or similar regulated lab.
• Practical knowledge of analytical testing techniques and laboratory documentation.
• Understanding of cGMP requirements and working in a regulated environment.
• Excellent written and verbal communication skills.
• Strong attention to detail and ability to work in a team.

Responsibilities

• Perform routine QC testing of water samples (TOC, pH, conductivity).
• Conduct raw material analysis using HPLC, KF, UV, IR and wet chemistry methods.
• Complete testing and documentation accurately and on time.
• Ensure activities comply with SOPs, specifications, and quality standards.
• Author, review and update laboratory documentation and SOPs as needed.
• Investigate OOS results and support deviations and quality events.

Skills

Laboratory testing techniques

Documentation practices

Attention to detail

Communication skills

Team collaboration

Education

Third-level degree in Chemistry, Biology or related

Tools

HPLC

Karl Fischer (KF)

UV/Vis

IR spectroscopy

Job description

Role Overview

A leading biopharmaceutical organisation is seeking a QC Raw Materials Specialist to join its Quality Control Materials team at a state-of-the-art biologics manufacturing facility in Dublin.

This is an excellent opportunity to join a high-performing laboratory team supporting the manufacture of biologic drug substances. The role offers exposure to a diverse range of raw material, water, and in-process testing activities, alongside opportunities to contribute to regulatory compliance, technical transfers, laboratory documentation, and continuous improvement initiatives.

Reporting to the QC Raw Materials Manager, the successful candidate will perform laboratory testing and support site quality activities in accordance with current Good Manufacturing Practice (cGMP) requirements and established quality standards.

Key Responsibilities

• Perform routine quality control testing of water samples, including Total Organic Carbon (TOC), pH, and conductivity.
• Conduct raw material analysis using a range of analytical techniques, including HPLC, Karl Fischer (KF), UV, IR, and wet chemistry methods.
• Complete laboratory testing and associated documentation accurately and within required timelines.
• Ensure all activities are performed in compliance with approved Standard Operating Procedures (SOPs), registered specifications, and applicable quality standards.
• Author, review, and update laboratory documentation and SOPs as required.
• Review analytical results and reconcile laboratory records, ensuring out-of-specification (OOS) results are investigated in accordance with established procedures.
• Support the technical transfer and implementation of new projects and testing methods.
• Assist with OOS investigations, deviations, and other quality events.
• Manage laboratory samples and maintain accurate sample traceability and chain of custody using electronic laboratory and sample management systems.
• Maintain awareness of relevant regulatory requirements, industry standards, and compliance trends affecting laboratory operations and pharmaceutical manufacturing.
• Undertake additional laboratory duties as required by the QC laboratory management team.

Candidate Profile

The successful candidate will be detail-oriented, quality-focused, and motivated to develop their technical expertise within a collaborative, regulated laboratory environment. They will play an important role in supporting reliable testing, maintaining data integrity, and ensuring the continued quality of manufacturing operations.

Essential Requirements:

• A minimum of a third-level degree in Chemistry, Biology, or a related scientific discipline.
• At least 2-3 years of experience working in a pharmaceutical, healthcare, biopharmaceutical, or comparable technical laboratory environment.
• Practical knowledge of analytical testing techniques and laboratory documentation.
• An understanding of cGMP requirements and the importance of working in a regulated environment.
• Excellent written and verbal communication skills.
• Strong attention to detail, organisational skills, and the ability to work effectively as part of a team.