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Junior Lab CSV IT Engineer 1736
On-site in Co. Cork·Full-time·Added 4 days ago (last checked 23 Oct)
Our summary
- Work mode
- On-site, Co. Cork
- Contract
- Full-time
Skills
Nice to have
Requirements
What we're looking for
- Bachelors degree in Engineering, Computer Science, or a related technical discipline.
- 1-3 years' experience in a regulated pharmaceutical, biotechnology, medical device, or laboratory environment.
- Basic understanding of CSV, SDLC, and GMP principles.
- Strong attention to detail and documentation skills.
- Good communication skills and willingness to learn.
- Ability to work collaboratively within cross-functional teams.
Nice to have
- Exposure to validation documentation and testing activities is advantageous.
- Familiarity with laboratory systems such as LIMS, CDS, ELN, LabVantage, or similar platforms is desirable.
Pay & benefits
What you'll get
What SimoTech Can Offer
- Role provides a high degree of autonomy to allow the successful candidate to reach their full potential.
- Develop new skills and enhance technical ability by working with innovative technologies in a multi-disciplined environment.
- Opportunity to work with large corporate clients on exciting capital projects.
The role
Why SimoTech
What is it like to work at SimoTech? With a strong collaborative teamwork culture based on respect, trust and excellence, we play a critical partnering role to our clients’ life-changing supply of products to patients. In return, there is excellent salary, benefits, career progression, educational support and much more.
Junior Lab CSV IT Engineer 1736
SimoTech is seeking a Junior Lab IT CSV Engineer to support laboratory system validation and compliance activities for our biopharma client in Co. Cork.
In this role, you will support the implementation, validation, and ongoing support of laboratory computerised systems while working alongside experienced CSV, Quality, and IT professionals. You will gain hands-on experience across system lifecycle activities, contributing to projects that support the development and manufacture of life-changing medicines within a highly regulated GMP environment.
This is an excellent opportunity to accelerate your career, develop valuable technical and compliance knowledge, and make a meaningful impact from day one.
What you'll do
Key Responsibilities
- Support validation activities for laboratory computerised systems under the guidance of senior team members.
- Assist with the preparation and execution of validation protocols and test scripts.
- Contribute to the generation and maintenance of validation documentation.
- Participate in risk assessments, change controls, and document reviews.
- Support the collection and organisation of validation evidence and test records.
- Assist with system periodic reviews and compliance monitoring activities.
- Work with Laboratory, Quality, and IT teams to resolve validation-related issues.
- Support inspection and audit readiness activities.
- Coordinate system and test data availability with laboratory teams to support test execution.
- Ensure work is completed in accordance with GMP, Data Integrity, and company procedures.
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