Vilnius, Lithuania, Lithuania
Onsite
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
About Thermo Fisher Scientific
At Thermo Fisher Scientific, we develop solutions that help people live healthier, cleaner, and safer lives. This is more than our mission—it is the impact our colleagues make every day.
At our Vilnius site, we develop and manufacture innovative life science and diagnostic technologies used by researchers, clinicians, and laboratories around the world. Our teams work with advanced manufacturing, laboratory, automation, and quality systems that support reliable operations and high-quality products.
Join a collaborative environment where technology, quality, compliance, and continuous improvement come together to support products used globally.
Job Overview
We are looking for a CSV Validation Engineer to join our team and support computerized systems and automation validation activities across manufacturing, laboratory, quality, and technical environments.
In this role, you will work at the intersection of technology, quality, automation, and regulated operations. You will help validate computerized and automated systems that support manufacturing, laboratories, quality processes, and product delivery, ensuring they are reliable, compliant, and fit for intended use.
You will support validation throughout the system lifecycle — from requirements, risk assessment, testing, and documentation to deviation management, change control, periodic review, and ongoing compliance.
Previous job title does not need to be “CSV Engineer”. We welcome candidates from validation, automation, IT systems, quality, laboratory systems, engineering, or regulated manufacturing backgrounds who want to grow in computerized systems validation.
This is a great opportunity to build expertise in Computerized Systems Validation (CSV), GAMP5 principles, data integrity, and GMP compliance while working in a growing international life sciences organization.
You will collaborate closely with Quality, IT, Automation, Engineering, Manufacturing, Laboratory Operations, and Technical Operations teams.
Key Responsibilities
Plan, coordinate, and execute computerized systems validation activities
Support validation of systems used in manufacturing, laboratory, quality, automation, and technical operations
Prepare, review, and execute validation documentation, including requirements, risk assessments, test protocols, reports, procedures, and related records
Support system lifecycle activities, including system implementation, changes, periodic reviews, and decommissioning
Apply GAMP5, GMP, data integrity, and applicable regulatory principles to validation activities
Identify, document, and investigate deviations related to validation execution
Support corrective and preventive actions to ensure timely and effective issue resolution
Collaborate with IT, Automation, Quality, Manufacturing, Engineering, and Laboratory teams
Act as a point of contact for computerized systems validation activities with internal stakeholders
Support continuous improvement initiatives related to CSV processes, documentation, testing, and compliance
Coordinate external vendors or technical specialists during validation activities when required
Experience and Qualifications
Advanced degree in Engineering, Life Sciences, Chemistry, Biotechnology, Information Technology, Automation, Computer Science, or another related technical field
or
Bachelor’s degree with at least 2 years of relevant experience in validation, quality, IT systems, automation, engineering, manufacturing, laboratory operations, or another regulated environment
Experience in GMP, ISO, pharmaceutical, biotechnology, medical device, diagnostics, laboratory, manufacturing, automation, or another regulated technical environment would be an advantage
Experience with systems, software, automation, quality documentation, validation, testing, or technical project work would be beneficial
Skills and Competencies
Interest in computerized systems validation, system qualification, automation, or regulated technical processes
Strong technical writing skills and ability to prepare clear, structured documentation
Analytical thinking and structured problem-solving skills
Ability to work with data, identify risks, and support evidence-based decisions
Good understanding of documentation, traceability, testing, and change control principles
Strong organizational skills and ability to manage several priorities at once
Good communication skills and ability to collaborate with technical and non-technical teams
Proficiency in Microsoft Office tools
Good written and spoken English skills
Ability to work in regulated production or laboratory environments when required
Preferred Qualifications
Experience with Computerized Systems Validation (CSV)
Knowledge of GAMP5, GMP, ISO, FDA regulations, data integrity, or electronic records principles
Experience with automation systems, LIMS, MES, ERP, QMS, SCADA, PLC, or laboratory software
Experience with validation or testing in GMP or another regulated environment
Experience with IQ/OQ/PQ, system testing, risk assessment, or gap analysis
Knowledge of quality management systems and regulated documentation practices
Experience managing validation or technical projects independently
Knowledge of statistical analysis, process control, or data analysis tools
What We Offer
Annual performance bonus and additional financial benefits
Comprehensive health package, including private health, life and accident insurance
Wellbeing support for employees and their family members, including mental health consultations, health check-ups, vaccinations, and on-site health initiatives
Opportunities for professional growth through internal training, access to Thermo Fisher e-University, and continuous development
The opportunity to work in a global, innovation-driven organization and collaborate with international teams
Daily benefits such as subsidized meals, gym access, and company transportation
An inclusive and supportive culture, with team events and community initiatives
2 additional paid volunteering days per year
We are an equal opportunity employer and value diversity. All qualified applicants will receive consideration regardless of race, religion, gender, age, disability, veteran status, sexual orientation, gender identity, or any other protected characteristic.
How to Apply
If you are interested in computerized systems validation, automation, quality, technology, and continuous improvement — and want to grow your career in a global life sciences organization — we would love to hear from you.
Even if your experience covers only part of the CSV field, but you are motivated to learn and develop in this area, we encourage you to apply.
Compensation
The monthly salary range estimated for this position based in Lithuania is €2 183,33–€3 270,83.Want to know if this job is worth applying to?