Bioassay Analyst – GMP Lab Data & QC Specialist

Eurofins; Ringaskiddy; On-site; EUR 32,000 - 42,000; Full time

Benefits offered by this job

Pension

Private Medical Insurance

Life assurance

Annual discretionary bonus

Birthday Holiday entitlement

Job summary

Eurofins is hiring a BioAssay Analyst in Cork to join a GMP‑regulated lab environment. You will perform analytical and bioassay testing, manage sample receipt and tracking, maintain equipment, and ensure QA standards while contributing to continuous improvement. This is a full‑time, permanent role with biweekly rotating shifts (07:00–19:00) and client‑site operations.

We value attention to detail, strong data integrity, and collaborative teamwork within a highly regulated life sciences setting.

Qualifications

• Degree in a scientific discipline with GMP experience preferred.
• Practical knowledge of analytical techniques (HPLC, ELISA, UV).
• Experience with LIMS and maintaining compliant records.
• Strong attention to detail and data integrity.
• Excellent communication and teamwork abilities.

Responsibilities

• Perform analytical and bioassay testing per pharmacopeial and Eurofins standards.
• Manage receipt, distribution and tracking of samples in the lab.
• Maintain expertise in analytical techniques and update SOPs as needed.
• Ensure proper use, calibration and maintenance of lab equipment.
• Investigate deviations, propose process improvements and cost efficiencies.
• Train and support colleagues and cover shifts as required.

Skills

Scientific degree

GMP experience

Analytical skills

LIMS experience

Attention to detail

Communication

Education

Bachelor's degree in a scientific discipline

Tools

HPLC

Capillary SDS

Capillary IEF

ELISA

UV analysis

LIMS

Job description

Eurofins is hiring a BioAssay Analyst in Cork to join a GMP‑regulated lab environment. You will perform analytical and bioassay testing, manage sample receipt and tracking, maintain equipment, and ensure QA standards while contributing to continuous improvement. This is a full‑time, permanent role with biweekly rotating shifts (07:00–19:00) and client‑site operations.

We value attention to detail, strong data integrity, and collaborative teamwork within a highly regulated life sciences setting.