Senior QC Analyst, Biotech | Quality & CI Lead

Headcount Solutions Polska Sp. z o.o.; Dublin; On-site; EUR 60,000 - 90,000; Full time

Job summary

Headcount Solutions Polska Sp. z o.o. seeks a Senior QC Analyst to join the Quality Team at a leading Biologics facility in West Dublin. The role supports startup activities and performs biological, chemical and physical analyses to ensure cGMP compliance.

Key responsibilities include QC testing, collaboration with Process Development, Manufacturing Operations and ensuring readiness for QMR decisions while driving continuous improvement across the site.

Qualifications

• Bachelor's Degree in Science or related
• 4 years experience in Biotechnology/Pharmaceutical industry
• Understanding of cGMP requirements for Lab Operations
• Understanding of GMP, ICH, USP and Global Compendia regulations
• Experience with laboratory analysis methods (HPLC, GC, UPLC, Capillary Electrophoresis and Wet Chemistry)

Responsibilities

• Support Quality Control Testing hub across the site.
• Support lab startup activities conducting analyses.
• Collaborate with Process Development Technical Services and Manufacturing Operations.
• Provide information to support the QMR decision making process.
• Collaborate across the network and continuous improvement teams.
• Create strategies to manage risk within Quality Control operations.
• Identify and communicate risks across the site.
• Work across teams to meet and track schedules.
• Support project delivery and operational readiness.

Skills

Communication skills

Prioritization

Cross-functional collaboration

GMP/ICH/USP knowledge

Education

Bachelor's Degree in Science

Tools

HPLC

GC

UPLC

Capillary Electrophoresis

Wet Chemistry

Job description

Headcount Solutions Polska Sp. z o.o. seeks a Senior QC Analyst to join the Quality Team at a leading Biologics facility in West Dublin. The role supports startup activities and performs biological, chemical and physical analyses to ensure cGMP compliance.

Key responsibilities include QC testing, collaboration with Process Development, Manufacturing Operations and ensuring readiness for QMR decisions while driving continuous improvement across the site.