Quality Control Analyst

Morgan McKinley; Dublin; On-site; EUR 35,000 - 45,000; Full time

Job summary

A pharmaceutical recruitment agency is seeking a QC Analyst in Dublin. The role requires 1-2 years of analytical testing experience within a GMP lab, focusing on HPLC, KF, and FTIR. Responsibilities include performing QC tests, documenting laboratory work, and assisting with data analysis. The position is a 12-month contract offering a collaborative environment for problem-solving.

Qualifications

• 1 - 2 years of analytical testing experience in a cGMP regulated lab.
• Experience performing HPLC, KF, FTIR, wet chemistry in the pharmaceutical industry.
• Ability to work independently and recognize anomalous trends.

Responsibilities

• Perform QC testing (TOC, pH, Conductivity) of water samples.
• Complete laboratory documentation as directed by the QC Manager.
• Assist in updating and issuing documentation, including SOPs.

Skills

Analytical testing experience

HPLC proficiency

Experience with raw materials

Problem-solving ability

Team collaboration

Education

BSc. in Science/Chemistry/Biochemistry

Tools

Empower software

Job description

Overview

An excellent opportunity for a QC Analyst with 1 - 2 years analytical testing experience within a cGMP regulated pharmaceutical lab. Significant experience performing HPLC, KF, FTIR required. Experience working with raw materials within a pharmaceutical company is preferred.

12 month contract located in North Dublin.

Responsibilities

• Performing QC testing (TOC, pH, Conductivity) of water samples. Performing analysis of Raw Materials including HPLC, KF, UV, IR and wet chemistry techniques. Completion in a timely and accurate manner of laboratory documentation as directed by the QC Manager.
• Assisting in updating and issuing documentation, including SOPs, as required.
• Performing routine data analysis, assist in the investigation of OOS results, perform trending analysis and writing investigation reports.
• Accurately documenting laboratory work.
• Execute and assist in technical transfer and co-validation activities.
• Sample management activities - ensuring chain of custody is maintained using CIMS and LIMS
• Assisting with qualification of laboratory instruments.
• Data review based on demonstrated proficiency on assays.

Qualifications and Experience

• Previous experience performing QC testing within a regulated pharmaceutical or biopharmaceutical laboratory is required.
• Experience performing HPLC, KF, FTIR, wet chemistry tests within the pharmaceutical industry.
• Proficient user of Empower software.
• BSc. in Science/Chemistry/Biochemistry or related discipline.
• The successful candidate must demonstrate an ability to work independently and recognize anomalous trends or results.
• Must demonstrate problem solving ability, as well as the ability to prioritize objectives from multiple projects and adhere to scheduled timelines.
• Excellent communication and the ability to work in a team based collaborative environment are required.