Senior QC Analyst – Biotech Lab & Process Improvement

Aphex Group; Leinster; On-site; EUR 60,000 - 90,000; Full time

Job summary

Aphex Group seeks a QC Senior Analyst for the Analytical Laboratory at the Dunboyne facility in County Meath, Ireland. The role supports the Quality Control testing function and ensures compliance with cGMP and company regulations, delivering reliable analytical results.

You will work across self-directed work teams and hub teams to drive continuous improvement, mentor colleagues, and coordinate start-up activities for state-of-the-art analyses (HPLC, GC, UPLC, capillary electrophoresis) to

Qualifications

• Degree in Science/Technical/Quality or related field.
• 4 years' experience in biotechnology and/or pharmaceutical industry.
• Excellent written and oral communication skills.
• Understanding of cGMP requirements for Laboratory Operations and related systems.
• Ability to work on own initiative and within a team.
• Knowledge of analytical methodologies (HPLC, GC, UPLC, Capillary Electrophoresis, wet chemistry).
• Familiarity with GMP, ICH, USP and global compendia regulations and guidance.
• Experience with continuous quality/process improvement tools (e.g., Lean, Six Sigma, 5S).

Responsibilities

• Support Quality Control testing and hub/self-directed teams to ensure cGMP compliance.
• Assist with start-up activities for the analytical lab at the Dunboyne facility.
• Identify and resolve issues to enable timely delivery and quality.
• Coach and mentor self-directed teams in problem solving.
• Collaborate across cross-functional teams to meet site objectives and manage risks.

Skills

Quality control

Analytical thinking

Stakeholder management

Problem solving

Project management

Continuous improvement

Team collaboration

Communication (written)

Education

Science/Technical/Quality degree

Job description

Aphex Group seeks a QC Senior Analyst for the Analytical Laboratory at the Dunboyne facility in County Meath, Ireland. The role supports the Quality Control testing function and ensures compliance with cGMP and company regulations, delivering reliable analytical results.

You will work across self-directed work teams and hub teams to drive continuous improvement, mentor colleagues, and coordinate start-up activities for state-of-the-art analyses (HPLC, GC, UPLC, capillary electrophoresis) to