Senior Quality Control Analyst – Analytical Laboratory

RECRUITERS; Dunboyne; On-site; EUR 51,000 - 57,000; Full time

Job summary

Senior QC Analyst – Analytical Laboratory in Dunboyne, Co. Meath.

Our client, a leading global biopharmaceutical company, operates a state-of-the-art facility and seeks an experienced professional to support QC activities across analytical testing, stability, drug substance testing and validation. This onsite role requires a degree in Science or a related discipline and substantial pharma/biopharma experience with UPLC and CE/PA800, plus strong knowledge of cGMP and GDP.

Qualifications

• Degree in Science, Technical, Quality or related discipline.
• Pharma/biopharma industry experience essential – no graduates.
• Experience with UPLC, CE/PA800, raw materials, deviations and compliance.
• Experience with stability testing, drug substance testing and validation.

Responsibilities

• Perform stability, drug substance testing and validation activities.
• Conduct analytical testing using UPLC and CE/PA800.
• Support raw material/incoming goods testing and release.
• Manage and support deviations, compliance and quality-related issues.
• Ensure laboratory activities and documentation comply with cGMP and GDP.
• Communicate quality requirements to suppliers and support continuous improvement.

Skills

Analytical testing

cGMP knowledge

Communication skills

Team collaboration

Education

Science degree

Tools

UPLC

CE/PA800

Lab instrumentation

Job description

Senior QC Analyst – Analytical Laboratory

Our client is a leading global biopharmaceutical company operating a state-of-the-art biologics manufacturing facility in Dunboyne, Co. Meath, focused on delivering innovative medicines through advanced manufacturing and quality systems.

We are seeking an experienced Senior QC Analyst to join a leading biopharmaceutical manufacturing facility in Dunboyne, supporting critical QC activities across analytical testing, stability, drug substance testing and validation within a highly regulated GMP environment.

Key Responsibilities

• Perform stability, drug substance testing and validation activities.
• Conduct analytical testing using UPLC and Capillary Electrophoresis (CE/PA800).
• Support raw material/incoming goods testing and release in line with quality procedures and regulatory requirements.
• Manage and support deviations, compliance and quality-related issues.
• Ensure laboratory activities and documentation comply with cGMP and Good Documentation Practices (GDP).
• Communicate quality requirements to suppliers and support continuous improvement.

Requirements

• Degree in Science, Technical, Quality or related discipline.
• Previous pharmaceutical/biopharmaceutical industry experience is essential – no graduates.
• Experience with UPLC, CE/PA800, raw materials, deviations and compliance.
• Experience with stability testing, drug substance testing and validation.
• Strong knowledge of cGMP laboratory requirements.
• Excellent communication and organisational skills.
• Able to work independently and effectively within a team.

Location

Dunboyne, Co. Meath

Work Arrangement

Onsite

Salary

This opportunity is an on-site position based in Dunboyne, Co. Meath, offering a salary of €54,000 per annum.