Junior Lab IT CSV Engineer - GMP/Pharma Growth

SimoTech; Cork; On-site; EUR 42,000 - 65,000; Full time

Benefits offered by this job

Educational support

Career progression

Job summary

SimoTech, based in Ireland, is hiring a Junior Lab IT CSV Engineer to support validation of laboratory computerised systems in a GMP environment. You will collaborate with CSV, Quality and IT teams to implement, validate, and maintain systems used in biopharma manufacturing.

You will gain hands-on experience across the lifecycle, contribute to validation documentation, and develop critical compliance skills with educational support and mentorship.

Qualifications

• Bachelor's degree in a technical discipline.
• 1–3 years' experience in a regulated pharmaceutical/biotech/lab environment.
• Basic understanding of CSV, SDLC and GMP principles.
• Strong attention to detail and documentation skills.
• Good communication and willingness to learn.
• Ability to work collaboratively in cross-functional teams.
• Familiarity with LIMS/CDS/ELN/LabVantage is advantageous.

Responsibilities

• Support validation activities for laboratory computerised systems under supervision.
• Assist with validation protocols and test scripts.
• Contribute to generation and maintenance of validation documentation.
• Participate in risk assessments, change controls and document reviews.
• Support collection and organisation of validation evidence and test records.
• Assist with system periodic reviews and compliance monitoring.
• Coordinate with lab, quality and IT teams to resolve issues.
• Support inspection and audit readiness activities.
• Ensure work complies with GMP, data integrity and procedures.

Skills

CSV concepts

SDLC knowledge

GMP awareness

Documentation skills

Team collaboration

Education

Bachelors in Engineering/CS

Tools

LIMS

CDS

ELN

LabVantage

Job description

SimoTech, based in Ireland, is hiring a Junior Lab IT CSV Engineer to support validation of laboratory computerised systems in a GMP environment. You will collaborate with CSV, Quality and IT teams to implement, validate, and maintain systems used in biopharma manufacturing.

You will gain hands-on experience across the lifecycle, contribute to validation documentation, and develop critical compliance skills with educational support and mentorship.