Hybrid QC Finish Product Analyst

MS0234 GE Healthcare Ireland Limited; Cork; Hybrid; EUR 42,000 - 54,000; Full time

Job summary

GE Healthcare Ireland Limited is seeking a QC Finish Product Analyst to ensure finished product quality through compliant pharmaceutical testing and documentation. The role combines laboratory analysis, regulatory compliance, investigations, and cross-functional support.

Responsibilities include performing routine analyses (HPLC, osmolality, iodine analysis, pH, etc.), managing LIMS data, supporting stability programs, and contributing to batch release documentation and trend reporting.

Qualifications

• A third level Science Qualification.
• Minimum 1–2 years pharmaceutical GMP laboratory experience.

Responsibilities

• Carry out routine analysis on Finished Product samples ensuring compliance with cGLP/cGMP and that turnaround times are met.
• Assisting in the maintenance of the stability program and active involvement in investigations.
• Logging of samples in LIMS and entering results, ensuring results are within specification and task approval.
• Assist in audits and provide trends/CPV data; develop expertise in analytical testing to solve issues.

Skills

HPLC

Osmolality

Iodine analysis

Chromatography

Education

Bachelors in science

Tools

LIMS

GMP

Job description

GE Healthcare Ireland Limited is seeking a QC Finish Product Analyst to ensure finished product quality through compliant pharmaceutical testing and documentation. The role combines laboratory analysis, regulatory compliance, investigations, and cross-functional support.

Responsibilities include performing routine analyses (HPLC, osmolality, iodine analysis, pH, etc.), managing LIMS data, supporting stability programs, and contributing to batch release documentation and trend reporting.