Senior QC Analyst – Biopharma (Stability, UPLC & CE)

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 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.