Vilnius, Lithuania, Lithuania
Onsite
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)Job 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, and quality systems that help ensure reliable operations and high-quality products.
Join a collaborative environment where engineering, quality, technology, and continuous improvement come together to support products used globally.
Job Overview
We are looking for a Validation Engineer to join our team and support equipment, systems, facilities, and process qualification activities across manufacturing, laboratory, and technical environments.
In this role, you will help ensure that equipment and processes are properly qualified, compliant, and ready to support reliable operations. You will work with modern production and laboratory equipment, prepare and execute validation documentation, investigate deviations, and support continuous improvement across regulated processes.
This is a great opportunity for someone with an engineering, life sciences, chemistry, technical operations, quality, manufacturing, or laboratory background who wants to grow in validation and qualification.
Previous job title does not need to be “Validation Engineer”. We welcome candidates from engineering, maintenance, manufacturing, laboratory, technical operations, quality, or regulated environments who want to develop in this field.
You will collaborate closely with Manufacturing, Quality, Engineering, Technical Operations, Maintenance, Laboratory, and external contractor teams.
Key Responsibilities
Plan, coordinate, and execute qualification and validation activities for equipment, systems, facilities, and processes
Maintain validation schedules and help ensure equipment remains in a qualified state
Prepare, review, and execute qualification documentation, including IQ/OQ/PQ protocols, procedures, and summary reports
Support qualification activities for standard and customized equipment used in regulated environments
Identify, document, and investigate discrepancies, deviations, and validation-related issues
Define and implement corrective actions in collaboration with cross-functional teams
Act as the main point of contact for qualification activities with internal stakeholders
Coordinate technicians, contractors, and external specialists during qualification activities when needed
Support process improvements related to validation documentation, execution quality, and compliance
Experience and Qualifications
Advanced degree in Engineering, Life Sciences, Chemistry, Biotechnology, or another related technical field
or
Bachelor’s degree with at least 2 years of relevant experience in validation, qualification, engineering, quality, manufacturing, laboratory operations, or another regulated environment
Experience in GMP, ISO, pharmaceutical, biotechnology, medical device, diagnostics, manufacturing, laboratory, or another regulated technical environment would be an advantage
Skills and Competencies
Understanding of equipment qualification, process validation, or regulated technical processes
Experience with IQ/OQ/PQ protocols and validation documentation would be an advantage
Knowledge of GMP, ISO, FDA regulations, GAMP5, or other industry standards would be beneficial
Strong technical writing skills and ability to prepare clear, structured documentation
Analytical thinking and structured problem-solving skills
Ability to assess risks, identify gaps, and support evidence-based decisions
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 and Lithuanian skills
Ability to work in cleanroom or regulated production/laboratory environments when required
Preferred Qualifications
Experience with equipment qualification or process validation
Experience working with production, laboratory, utility, or facility systems
Knowledge of quality management systems and regulated documentation practices
Experience with risk assessments, gap analysis, deviation investigations, or CAPA
Experience coordinating contractors or technical service providers
Knowledge of calibration, metrology, statistical analysis, or process control methods
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 equipment qualification, validation, 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 validation 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?