Laisvų darbo vietų sąrašas

• Bachelor’s degree in Engineering or another technical/scientific discipline
• Strong verbal & written communication skills in English and Lithuanian
• Proven analytical & problem-solving ability
• Attention to detail and accuracy in documentation and analysis
• Proficiency with MS Office tools (Word, Excel, Outlook etc.)
• Ability to work collaboratively across multiple departments
• Willingness to adapt and take initiative

• Experience in manufacturing or process engineering
• Understanding of Risk Management principles and standards (e.g. ISO 31000, ISO 14971)
• Experience in preparing and reviewing technical documentation/drawings
• Ability to lead discussions on risk causes, effects & controls
• Experience in a regulated industry (medical, pharmaceutical etc.)

• Become an important part of a growing international company
• Engage in complex and meaningful work in Risk Management
• Access internal and external training for constant professional growth
• Experience supportive and collaborative team environment
• Competitive salary, based on experience and skills (from 2200 to 2600 Eur / month before taxes)
• Annual appraisals
• Timely holidays and no overtime
• Free company transportation to/from work (Vilnius-Pabradė-Vilnius only)
• Free gym access (Pabradė only) and access to nature areas nearby

• Good verbal & written communication in English and Lithuanian
• High level of accuracy and attention to detail
• Good organization & time management skills
• Basic IT proficiency (Word, Excel, Outlook etc.)
• Ability to work well with others and solve problems collaboratively
• Willingness to learn and develop new skills

• Degree level education (preferably in a technical or scientific field)
• Industrial experience
• Experience in document preparation and data management
• Basic understanding of manufacturing processes
• Awareness of international standards and regulations

• Become an important part of a growing international company
• Gain hands-on experience in Risk Management documentation and systems
• Access internal and external training for constant professional growth
• Experience supportive and collaborative team environment
• Competitive salary, based on experience and skills (from 1800 to 2200 Eur / month before taxes)
• Annual appraisals
• Timely holidays and no overtime
• Free company transportation to/from work (Vilnius-Pabradė-Vilnius only)
• Free gym access (Pabradė only) and access to nature areas nearby

• To manage material's projects, coordinate and guide the execution of the related activities;
• To liaise with external raw material suppliers and collaborate by organising material trials, providing requested information and giving support as needed to find the most suitable materials;
• To organise and participate (on demand) in injection moulding and extrusion trials;
• To develop, write and review related documents following established standards and templates;
• To read and analyse component’s drawing;
• To manage component/product evaluations, data analysis;
• To find solutions to problems encountered during the testing independently or in collaboration with other departments;
• To learn new skills, adapt to new methodologies and develop an in-depth knowledge of our product portfolio and the respiratory device industry;
• To compile relevant regulatory documentation in accordance with ISO standards/medical regulations and supporting transfer to production, with post market support.

• Bachelor’s degree in the fields of Chemistry/Engineering/Bioengineering/ Biomechanics/Physics or similar;
• Good English language skills (written and oral), as this is the main working language in the company;
• Good computer and MS Office skills: MS Word, MS Excel, MS Outlook.

• Good planning, organizational and project management skills.
• Good communication skills, ability to work both in a group and independently, thoroughness and diligence;
• Ability to function effectively across a number of interrelated departments;
• Good level of accuracy and attention to details: it is vital to pay attention to every test result and measurement, noticing when something is not quite right.
• Good problem solving skills with a hands-on approach.

• Job experience in chemistry/medical industry/manufacturing/quality area/project coordination (would be a plus);
• Awareness of International Standards and Regulations.

• Interesting work in an ever growing UAB “Intersurgical” company (in Pabrade or Visaginas);
• Internal and external training for constant professional growth;
• Friendly, positive and supportive attitude in the team;
• Possibilities to travel to exhibitions/conferences in Lithuania and abroad;
• Great opportunity to develop skills, get international experience and advance your career;
• Free gym access in Pabrade and beautiful nature for a walk during your lunch break;
• Free company transportation to/from work (Vilnius-Pabrade-Vilnius);
• Salary from 2300 to 3000 Eur before taxes (depends on background and experience);
• Annual appraisals;
• Timely holidays and no overtime.

• Requirements Gathering: Engage with stakeholders to elicit detailed business requirements, focusing on understanding the current (As-Is) processes and the desired changes leading to the (To-Be) state.
• Process Documentation: Document and map out future business processes.
• To-Be Process Design: Envision, design, and articulate desired future processes, ensuring that they align with the capabilities and benefits of the MES and Dynamics integration.
• Stakeholder Communication: Serve as a liaison between the technical team, project manager, and business stakeholders, ensuring clarity in communicating requirements, current processes, and envisaged changes.
• Gap Analysis: Compare the As-Is and To-Be states to identify gaps, challenges, and opportunities that the new systems should address.
• Business Change Impact Assessment: Evaluate the broader implications of transitioning from the As-Is to the To-Be states, highlighting areas requiring particular attention in change management strategies.
• Solution Evaluation: Work alongside the technical team to design solutions, ensuring they meet the To-Be requirements, and evaluate their feasibility, costs, and benefits.
• Quality Assurance & Testing: Validate that the developed solution matches the functional specifications and bridges the gap between the As-Is and To-Be states.
• Feedback Loop: Establish feedback mechanisms, ensuring the evolving solution remains aligned with business needs.
• Training & Support: Assist in creating training materials based on the To-Be processes, and provide support during the early stages of system adoption.
• Continuous Improvement: Post-implementation, monitor the effectiveness of the To-Be processes, gather feedback, and recommend further refinements or enhancements.

• Strong analytical skills, methodical, logically thinking
• Communication and presentation skills in English and Lithuanian
• Ability to work alone and within teams

• Computer knowledge: MS Word, MS Excel, MS Visio
• Experience / understanding of manufacturing systems

• Interesting and challenging work, growth opportunity
• Great opportunity to develop skills and experience
• Friendly and supportive team
• Career opportunities in fast developing new business function
• Company’s transportation to/from work
• Salary 1800-2800 Euro/month before taxes

• Higher/university education (law, medicine, pharmacy, engineering, or other related scientific studies);
• Knowledge of the regulatory requirements applicable for medical devices.
• Experience in the field of medical device regulation and/or quality;
• Excellent written and spoken English and Lithuanian;
• Good communication skills;
• Attention to detail and accuracy in documentation and analysis;
• Proficiency with MS Office tools (Outlook, Teams, Word, Excel, etc.)
• Ability to work collaboratively across multiple departments;
• Willingness to adapt and take initiative.

• Understanding of regulatory requirements for medical devices according to European Union, MDSAP, or United Kingdom regulations and recommendations;
• Knowledge of Quality Management System principles according to ISO9001, ISO13485 requirements;
• Experience in analysing and evaluating regulatory documents;
• Experience in project management;
• Experience in a regulated industry (medical, pharmaceutical etc.);
• Knowledge of Intersurgical processes and products;
• Knowledge of harmonised and international standards applicable to medical devices;
• Ability to read and understand technical documents related to medical devices.

• Become an important part of a growing international company;
• Engage in complex and meaningful work in Regulatory team;
• Access internal and external training opportunities;
• Experience a supportive and collaborative team environment;
• Competitive salary based on experience, knowledge, and skills (from 2100 to 2700 Eur/month before taxes);
• Annual appraisals;
• Timely holidays and no overtime;
• Free company transportation by bus to/from work (Vilnius-Pabradė-Vilnius only);
• Free gym access (Pabradė only).

• Pakrauti ir iškrauti atvykusius/išvykstančius krovinius ir patikrinti gauto kiekio atitikimą važtaraščiui
• Pagal pardavimų ir gamybos skyrių suplanuotus išvežimus numatytai dienai paruošti produkciją atitinkamai pagal pateiktą nomenklatūrą, vadovaujantis ruošimo instrukcijomis
• Užtikrinti sandėlyje esančių materialinių vertybių ir prekių saugojimą
• Gamybos/liejimo užsakymų rinkimas

• Geri lietuvių kalbos įgūdžiai;
• Geri darbo su kompiuteriu įgūdžiai (MS Office programos);
• Atsakingumas, kruopštumas, nuoseklumas, gebėjimas dirbti individualiai ir komandoje;
• Geri bendravimo įgūdžiai;
• Imlumas naujovėms ir pokyčiams;
• Noras mokytis ir tobulėti.

• Vidurinis/profesinis išsilavinimas;
• Patirtis sandėlininko pareigose;
• Autokrautuvo pažymėjimas;
• Anglų kalbos žinios.

• Įdomų ir iššūkių kupiną darbą pasaulinio lygio įmonėje projektuojančioje, gaminančioje ir į visą pasaulį tiekiančioje aukštos kokybės medicinos prietaisus, skirtus kvėpavimo palaikymui;
• Nemokamą atvykimą/parvykimą iš Švenčionių/Švenčionėlių/Molėtų
• Sveikatos draudimą nuo traumų;
• Apmokymus darbo vietoje;
• Darbo aprangą;

• Darbo grafikas – pamaininis slenkantis. Pirma pamaina - nuo 6 iki 15 val., antra – nuo 15 iki 24 val.

• Darbas gamyboje, medicininių kvėpavimo sistemų surinkimas, testavimas, pakavimas
• Darbas pamainomis (pirma diena nuo 8 val. iki 20 val., antra pamainos diena naktinė nuo 20 val. iki 8 val. ir dvi poilsio dienos). Galimi ir kiti lankstūs grafikai darbui po 12 val. Teirautis pokalbio metu.
• Dirbama švariose, kvalifikuotose patalpose.
• Apranga, avalyne bei kitomis reikalingomis darbui priemonėmis pasirūpiname.

• Vidurinis/profesinis/pagrindinis išsilavinimas;
• Noras dirbti

• Sugebėjimas greitai dirbti.
• Galimybė tobulėti, mokytis pameistrystės forma bei kilti karjeros laiptais

• gamybinių ir bendrųjų patalpų valymas ir priežiūra;
• pamaininis darbas 4 darbo dienos po 8 val. pirmoje pamainoje (6-15 val.), dvi poilsio dienos, 4 darbo dienos antroje pamainoje (15-24 val.), slenkantis grafikas.

• mokėti dirbti su valymo įrankiais ir įranga;
• kruopštumas, nuoseklumas, atsakingumas, gebėjimas dirbti individualiai ir komandoje.

• 6,79 Eur/val. su mokesčiais (maždaug nuo 1000 iki 1200 per mėnesį su mokesčiais).

• Gamyboje esančių įrenginių priežiūra, derinimas, remontas
• Planinių darbų atlikimas
• Užsakymo keitimo metu: mechaninių dalių, medžiagų, receptų keitimas
• Automatizuotų ir neautomatizuotų įrenginių paleidimas/sustabdymas
• Dalyvavimas naujos įrangos diegime

• Vidurinis arba spec. vidurinis techninis išsilavinimas
• Darbo patirtis gamyboje arba panašioje darbo srityje
• Geri darbo su kompiuteriu įgūdžiai (MS Office programos)
• Noras mokytis ir tobulėti
• Atsakingumas, nuoseklumas, gebėjimas dirbti komandoje ir individualiai
• Galimybė dirbti 12h grafiku

• Mechatronikos pagrindai
• Elektrotechnikos pagrindai
• Anglų kalbos pagrindai

• Galimybę mokytis ir nuolat tobulėti
• Atsakingą ir įdomų darbą tarptautinėje kompanijoje
• Valandinį atlygį atitinkantį kompetencijos lygį 8,25 €/h – 9,67 €/h

• Įrenginių prevencinė priežiūra, remontas, modernizavimas ir tobulinimas
• Atsarginių dalių identifikavimas pagal gamintojo pateiktą dokumentaciją
• Techninių brėžinių ir schemų skaitymas, analizė bei jų pritaikymas praktikoje.
• Įsitraukimas į sisteminių gedimų analizės bei eliminavimo procesus
• Bendradarbiavimas su kitais padaliniais siekiant užtikrinti sklandų gamybos procesą

• Techninis išsilavinimas arba praktinė patirtis mechanikos, elektronikos, elektrotechnikos ar hidraulikos srityje
• Praktiniai įgūdžiai dirbant su mechaniniais, elektriniais įrankiais bei matavimo prietaisais
• Darbo su kompiuteriu įgūdžiai
• Iniciatyvumas, noras mokytis bei tobulėti
• Atsakingumas, nuoseklumas, gebėjimas dirbti komandoje ir individualiai
• Galimybė dirbti slenkančiu grafiku dvejomis pamainomis (I: 06h – 15h ir II: 15h – 24h) 4 d.d. ir 2d. laisvos

• Aukštasis, aukštesnysis techninis išsilavinimas (inžinerijos srityje)
• Darbo patirtis gamyboje arba panašioje darbo srityje
• Anglų kalbos žinios technikos srityje
• PLV (programuojamų loginių valdiklių) ir robotikos išmanymas
• Gebėjimas skaityti elektros, hidraulines ir pneumatines principines schemas.
• Patirtis dirbant su hidraulinėmis sistemomis

• Galimybę mokytis ir nuolat tobulėti
• Atsakingą ir įdomų darbą tarptautinėje kompanijoje
• Valandinį atlygį atitinkantį kompetencijos lygį nuo 11,30 €/h (~2050 €/mėn.)

• Review the output of the Intercompany Planning Process to ensure accurate demand capture.
• Generate and maintain the Rough-Cut Capacity Plan for Lithuania.
• Analyse capacity planning outputs to identify potential material shortages. Work with central logistics and procurement teams to resolve them.
• Support local production teams in helping to address capacity bottlenecks and other constraints.
• Review production work orders, investigate progress deviations, and initiate corrective actions into the capacity plan / production schedule where needed.
• Ensure minimum stock levels are set accurately and reviewed regularly.
• Provide weekly and monthly analysis and reporting, including:
  • Asset utilisation and capacity bottlenecks
  • Group back orders and potential stock-outs
  • Monthly production spend review with Site Managers

Essential Skills

• Good English and Lithuanian language knowledge.
• Analytical skills / thinking.
• Effective communication and collaboration skills.

Desirable Skills

• Ability to multitask and solve problems.
• Proactive and team oriented.
• Ability and desire to learn, improve, grow.

Why should you apply?

• Engaging work in medical device industry
• Training and support
• Competitive salary 2200÷2800 EUR before taxes (dependent on background and experience).
• Annual appraisals and career opportunities
• Wide exposure to manufacturing process and ability to create substantial added value

• Manage validation projects, coordinate and guide the execution of the validation activities.
• Develop and write validation documents following established standards and templates.
• Develop and run test protocols.
• Analyse and document test results.
• Develop and implement solutions to validation issues.
• Maintain validation documentation through the validation life cycle.
• Provide the relevant support for regulatory audits.

• Bachelor’s degree (preferably in Engineering or other exact sciences discipline). If you are interested, but do not have required degree, you may apply anyway to discuss other possibilities.
• Good verbal and written communication skills in English and Lithuanian.
• Good computer knowledge: MS Word, MS Excel, MS Outlook.
• Ability to work and interact with various personnel.

• Enthusiasm for working in a team – validation is a team activity, and you will need good verbal and listening skills to share information amongst the team members.
• Preference for a structured approach to working – your work will affect others in the overall validation team.
• Attention to detail – it is vital to pay attention to every test result and measurement, noticing when something is not quite right.
• Analytical thinking – as well as identifying when there is an issue, part of the role can be to suggest why there might be an issue and potential fixes.
• Good written communication skills – protocol and report writing is an essential part of the job.
• Time management – there is a timeline that needs to be followed.
• Initiative – new and inventive ways may be needed to challenge the processes and fix problems.

• Interesting and challenging work.
• Friendly environment and full training (internal: Instructor-led training, eLearning; external: webinars and online training).
• Great opportunity to develop skills and experience.
• Salary from 2200 to 2600 Eur before taxes (depends on background and experience).

• Manage validation plans and projects.
• Form a team of representatives from other departments to support an individual project.
• Identify acceptance criteria and develop test plans.
• Prepare validation protocols: IQ, OQ and PQ, write Final Reports.
• Execute validation protocols to verify that the equipment/system and method are fit for purpose.
• Develop and implement solutions to validation issues.
• Conduct periodic reviews and post-change reviews.

• Bachelor’s degree (engineering/physics/chemistry or another relevant field). If you are interested, but do not have required degree, you may apply anyway to discuss other possibilities.
• Good oral and written communication skills in Lithuanian and English.
• Computer knowledge: MS Word, MS Excel, MS Visio.
• Problem solving skills with a hands-on approach.
• Good accuracy and attention to detail.
• Ability to work both as part of a team and independently, and function effectively across interrelated departments.

• Job experience in medical device industry or other regulated industry, quality area.
• Planning, organizational and project management skills.

• Interesting and challenging work.
• Friendly environment and training.
• Great opportunity to develop skills and experience.
• Company’s transportation to/from work.
• Salary from 2200 to 2600 Eur (gross) (depends on background and experience).

• Darbas gamyboje, medicininių kvėpavimo sistemų surinkimas, testavimas, pakavimas
• Darbas prie automatinių surinkimo linijų – nustatyti įrenginio parametrus, atlikti įrenginio priežiūrą, stebėti, kad gaminiai atitiktų kokybės reikalavimus.
• Esant reikalui, bendrauti su inžinierinio aptarnavimo skyriumi.
• Darbas pamainomis (pirma diena nuo 8 val. iki 20 val., antra pamainos diena naktinė nuo 20 val. iki 8 val. ir dvi poilsio dienos). Galimi ir kiti lankstūs grafikai darbui po 12 val. Teirautis pokalbio metu.
• Dirbama švariose, kvalifikuotose patalpose.

• Vidurinis/profesinis techninis išsilavinimas.
• Noras dirbti.

• Sugebėjimas reaguoti į iškilusias gamybines problemas ir sprendimų priėmimas.
• Kandidatuojant į surinkimo įrengimų operatoriaus pozicija – profesinis techninis išsilavinimas.
• Kompiuterinio raštingumo žinios.

• kruopštumas, nuoseklumas, atsakingumas, gebėjimas dirbti individualiai ir komandoje.
• Darbas pamainomis (pirma diena nuo 8 val. iki 20 val., antra pamainos diena naktinė nuo 20 val. iki 8 val. ir dvi poilsio dienos). Galimi ir kiti lankstūs grafikai darbui po 12 val. Teirautis pokalbio metu.

• 7 Eur/val. su mokesčiais