Lab Systems Specialist

QCS Staffing Ltd; Dublin; On-site; EUR 45,000 - 65,000; Full time

Job summary

Quanta Consultancy Services Ltd is seeking a Lab Systems Specialist to join their team in Dublin, Ireland on a 6-month contract. This role offers a chance to work with innovative equipment and modern pharmaceutical technologies in a rapidly growing biopharma sector.

The ideal candidate will possess a relevant B.S. degree and proven experience in the biopharmaceutical industry. Responsibilities include maintaining master data in the EM system and managing change documentation.

Qualifications

• Extensive experience in the biopharmaceutical industry or equivalent.
• Admin experience with QC lab digital systems is desirable.

Responsibilities

• Create and maintain master data in the EM system.
• Execute appropriate change management processes.
• Document change control processes.
• Review and assess impact of method/specification changes.

Skills

GMP microbiological testing

LIMS

LES

MODA

Microsoft Office Applications

Education

Minimum B.S. degree in a relevant scientific, computer, or engineering program

Job description

Lab Systems Specialist – Ireland, Dublin – 6 Month Contract

Are you a Lab Systems Specialist looking for your next challenge in Dublin? A leading multinational in Ireland’s thriving biopharma industry is expanding their team for a major facility development. This project provides hands‑on experience with innovative equipment, large‑scale operations, and modern pharmaceutical technologies. It’s an ideal opportunity to build your skills within one of Europe’s fastest‑growing life‑science regions.

Responsibilities

• Create and maintain master data in the EM system, including plans and analytical methods.
• Execute appropriate change management processes to document creation and revision of master data.
• Execute and document change control processes.
• Review and assess the impact of method/specification changes to master data and recommend appropriate change actions.

Qualifications

• Minimum B.S. degree in a relevant scientific, computer, or engineering program.
• Extensive experience in the biopharmaceutical industry or an equivalent combination of education and experience.
• Experience with GMP microbiological testing is a plus.
• Admin experience with QC lab digital systems is desirable (e.g., LIMS, LES, or MODA).
• Proficient in Microsoft Office Applications and other relevant software programs.
• Ability to interpret and apply cGMPs, regulatory requirements, and industry best practices.