Senior Quality Control Analyst

Life Science Recruitment; Leinster; On-site; EUR 60,000 - 85,000; Full time

Job summary

Life Science Recruitment is seeking a QC Senior Analyst for a leading pharmaceutical organisation based in Louth. The role supports QC Manager/QC Associate Director to meet cGMP and cGLP requirements and ensure product quality and reliable supply.

Responsibilities include performing testing, supporting investigations, contributing to procedures and data integrity, and helping audit readiness. Degree-qualified candidates with 4 years’ lab experience are invited to apply.

Qualifications

• Degree in Science/Quality/Technical or related.
• 4 years of laboratory experience in biotech/pharma.
• Experience with Environmental Monitoring, Water Monitoring, Endotoxin Testing and Bioburden Testing.

Responsibilities

• Operate as part of the QC team performing allocated testing and lab duties.
• Act as testing SME with QC, participate in investigations and troubleshooting.
• Participate in QC Tier daily meetings and communicate progress and deviations.

Skills

Laboratory testing

Quality Systems

cGMP/cGLP compliance

Education

Degree in Science/Quality/Technical or related

Job description

We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Louth. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.

The QC Senior Analyst works as directed by the QC Manager/QC Associate Director according to company safety policies, cGMP and cGLP. Ensure that QC team objectives are effectively achieved, consistent with requirements to ensure compliance, safety and reliable supply to our customers.

Key Responsibilities:

• Operating as part of the QC team performing the allocated testing and laboratory-based duties.
• Act as testing SME with QC department, participate in OOS investigations and supporting troubleshooting activities.
• Participate in QC Tier daily meetings and ensure effective communication of testing progress, deviations, escalation of potential cGMP or compliance issues etc.
• Participate in writing/revising/ rolling out accurate operational procedures, training materials and maintenance procedures for various Quality systems.
• Peer review of testing documentation and ensuring data integrity compliance and QC Right First Time KPIs are achieved.
• Support activities including general lab readiness, audit readiness and audit participation, laboratory equipment qualification and analytical method technical transfer, verification and validation.
• Contributing to a continuous improvement environment and bringing problem solving and troubleshooting capabilities.
• Demonstrating a commitment to learning and personal development.

Education and Experience:

• Degree qualification (Science/Quality/Technical or related)
• 4 years of laboratory experience, including sampling, testing, reporting in the biotechnology and/or pharmaceutical industry.
• Experience with Environmental Monitoring, Water Monitoring, Endotoxin Testing and Bioburden Testing