QC Analyst

Role Summary:

• Our client, based in Co. Dublin, is looking for a QC Analyst to join their team on site based on a fixed term contract.

Core Duties and Responsibilities:

• Perform precise sampling of incoming raw materials in accordance with established protocols and SOPs.
• Conduct chemical, physical, and (if necessary) microbiological tests on raw materials using analytical techniques such as:
• High-Performance Liquid Chromatography (HPLC)
• Gas Chromatography (GC)
• Ultraviolet-Visible Spectroscopy (UV-VIS)
• Fourier-Transform Infrared Spectroscopy (FTIR)
• Titration, pH measurements, moisture analysis, and other relevant techniques.
• Compare test results against established specifications and ensure materials meet required quality standards before approval.
• Accurately record all test results in laboratory notebooks or data management systems such as LIMS.
• Review and verify supplier Certificates of Analysis (CoAs) to ensure conformity with internal quality standards.
• Issue reports on material quality and prepare internal Certificates of Analysis (CoAs) when necessary.
• Ensure raw material testing adheres to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant regulatory guidelines.
• Flag and report any non-conforming materials and deviations from specifications, initiating investigation processes where required.
• Work closely with procurement and supply chain teams to ensure raw material suppliers adhere to quality requirements and specifications.
• Communicate any material quality issues with suppliers and participate in supplier quality assessments and audits as needed.
• Collaborate with warehouse teams to ensure proper sampling and storage of raw materials.
• Regularly calibrate and maintain lab equipment such as HPLC, GC, and other instruments to ensure accurate test results.
• Troubleshoot equipment malfunctions and coordinate repairs or service when needed.
• Perform routine testing using techniques such as HPLC, GC, UV-VIS, and FTIR to analyse raw materials, in-process products, and finished goods.

Minimum Qualifications and Experience:

• Bachelor’s degree in chemistry, Biochemistry, Microbiology, or related field.
• 3 to 5 years of experience in a Quality Control Lab, preferably in pharmaceuticals, cosmetics, or FMCG.
• Hands-on experience with analytical instruments (HPLC, GC, FTIR) and familiarity with GMP/GLP.
• Strong attention to detail and ability to follow SOPs.
• Excellent written and verbal communication skills.
• Proficiency in data management systems (e.g., LIMS) and statistical analysis tools.

Please note, we do not require agency assistance with this role.