Chemikas (-ė) | Laboratorija, technologijos ir produktų vystymas
Pagrindinės atsakomybės
- Atlikti laboratorinius tyrimus ir eksperimentus
- Dalyvauti produktų kūrimo, gamybos ar technologinių procesų veiklose
- Dirbti su analitiniais metodais ir modernia laboratorine įranga
- Analizuoti tyrimų rezultatus bei rengti techninę dokumentaciją
- Prisidėti prie produktų kokybės užtikrinimo
- Dalyvauti naujų produktų kūrimo, validavimo ir procesų optimizavimo projektuose
- Bendradarbiauti su R&D, kokybės, gamybos ir kitomis komandomis
- Prisidėti prie nuolatinio procesų tobulinimo ir inovacijų diegimo
Patirtis ir kvalifikacijos
- Aukštasis išsilavinimas chemijos, analitinės chemijos, biochemijos, medžiagų mokslo, cheminės inžinerijos ar kitoje susijusioje srityje
- Kviečiame kandidatuoti tiek bakalauro, tiek magistro studijas baigusius specialistus
- Vertinsime tiek profesinę darbo patirtį, tiek laboratorinę praktiką ar mokslinių tyrimų patirtį studijų metu
Įgūdžiai ir kompetencijos
- Laboratorinio darbo pagrindai
- Domėjimasis chemija, analitiniais metodais ir technologijomis
- Analitinis mąstymas ir gebėjimas spręsti problemas
- Kruopštumas, atsakingumas ir dėmesys detalėms
- Gebėjimas dirbti savarankiškai ir komandoje
- Geri darbo kompiuteriu įgūdžiai
- Geros anglų kalbos žinios
- Noras mokytis, tobulėti ir augti profesinėje srityje
Vertinsime kaip privalumą - Patirtį ar žinias vienoje ar keliose iš šių sričių:
- Analitinė chemija
- Chromatografija (HPLC, UHPLC ar kt.)
- Medžiagų ar polimerų chemija
- Tirpalų, reagentų ar buferių ruošimas
- Laboratorinė įranga ir analitiniai metodai
- Kokybės kontrolė
- Produktų kūrimas ir technologijų vystymas
- Gamybos procesai
- GMP ar kitų kokybės sistemų principų išmanymas
Ką siūlome
- Metinį priedą už rezultatus ir papildomas finansines naudas
- Išsamų sveikatos paketą: privatus sveikatos, gyvybės ir nelaimingų atsitikimų draudimas
- Darbuotojų ir jų šeimos narių gerovės programą: psichologinės konsultacijos, sveikatos patikros, skiepai bei sveikatingumo iniciatyvos
- Profesinio augimo galimybes: vidiniai mokymai, prieiga prie Thermo Fisher e-University“ ir nuolatinis tobulėjimas
- Galimybę dirbti su modernia laboratorine įranga ir pažangiomis technologijomis
- Galimybę mokytis iš aukščiausio lygio savo srities specialistų Lietuvoje ir bendradarbiauti su tarptautinėmis komandomis
- Karjeros galimybes vienoje didžiausių pasaulio gyvybės mokslų organizacijų
- Kasdienes naudas: dalinai kompensuojamas maitinimas, sporto salė ir įmonės transportas
- Įtraukią ir palaikančią darbo kultūrą, komandos renginius bei bendruomenės iniciatyvas
- 2 papildomas apmokamas savanorystės dienas per metus
Kaip kandidatuoti
CSV Validation Engineer | Computer Systems & Automation Validation
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
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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 — apply here.
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
Validation Engineer | Equipment & Process Qualification
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.)
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 — apply here.
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 Lietuva is €2 183,33–€3 270,83.
Kitus UAB „Thermo Fisher Scientific“ darbo pasiūlymus galite rasti čia.