QC Chemistry Analyst — Biopharma QC (HPLC, GMP)

The Innopharma Group; Ireland; On-site; EUR 32,000 - 46,000; Full time

Job summary

Innopharma Group seeks QC Chemistry Analysts for roles across Ireland. The position covers analytical testing of raw materials, in-process samples, and finished products to meet quality standards.

Responsibilities include performing chemical analyses with HPLC, UV-Vis, and related techniques, documenting results per GMP, and supporting method validation, investigations, and deviations. Shift work may be required.

Qualifications

• Bachelor’s degree in Chemistry, Biochemistry, Analytical Chemistry or related discipline.
• 1–3 years’ experience in QC laboratory in pharmaceutical/biopharmaceutical industry.
• Knowledge of analytical instruments and techniques including HPLC, spectrophotometry and electrophoresis.

Responsibilities

• Perform routine and non-routine chemical analysis on raw materials, intermediates, finished products, and stability samples.
• Review, calculate, and document test results in accordance with GMP and data integrity requirements.
• Follow approved methods, SOPs, and test protocols; perform instrument calibration and troubleshooting.
• Support investigations of OOS/OOT and deviations; maintain lab safety and cleanliness.
• Assist with audits/inspections and continuous improvement; willingness to work shift.

Skills

Communication skills

English proficiency

Education

Bachelor's degree in Chemistry/Biochemistry/Analytical Chemistry

Tools

HPLC

Spectrophotometry

Electrophoresis

Job description

Innopharma Group seeks QC Chemistry Analysts for roles across Ireland. The position covers analytical testing of raw materials, in-process samples, and finished products to meet quality standards.

Responsibilities include performing chemical analyses with HPLC, UV-Vis, and related techniques, documenting results per GMP, and supporting method validation, investigations, and deviations. Shift work may be required.