Prisijunkite prie mūsų komandos

SURINKĖJA(-AS)

• 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

VALYTOJAS(-A)

• 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.

• 7,50 Eur/val. su mokesčiais 

VALIDATION ENGINEER (PABRADĖ)

• Perform qualification and validation of laboratory equipment/systems and methods.


• Manage validation plans and projects.


• Develop and execute validation protocols: IQ, OQ and PQ, write Final Reports.


• Collaborate with cross-functional teams (Quality, Technical and Development, IT, etc.) to ensure validation project timelines and quality expectations are met.


• 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).

OPERATORIUS IR SURINKIMO ĮRENGIMŲ OPERATORIUS (-ĖS) PABRADĖS PADALINYJE

• 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.

PROJECT COORDINATOR

• 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 verbal), 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.

RISK COORDINATOR (VISAGINAS OFFICE)

• 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

REGULATORY COMPLIANCE SPECIALIST

• Higher/university education (law, medicine, pharmacy, engineering, or other related scientific studies);


• Knowledge of the regulatory requirements applicable for medical devices;


• 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.

• Experience in the field of medical devices regulations or/and quality of medical devices.


• 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 and ISO13485 requirements;


• Experience in analysing and evaluating regulatory documents;


• Experience in project management;


• Experience in a regulated industry (medical devices, 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).

RISK ENGINEER (VISAGINAS OFFICE)

• 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

GAMINIŲ REGISTRACIMO SPECIALISTAS(-Ė)

• Rinkti, tikrinti, rengti bei siųsti dokumentus ir informaciją susijusią su laisvos prekybos sertifikatų išdavimu, bei reikalingą mūsų produktų registracijai;


• Komunikuoti su klientais, siekiant kuo aiškiau nustatyti laisvos prekybos sertifikatų išdavimo ar produktų registracijos reikalavimus;


• Padėti Gaminių registravimo administratoriui.

• Aukštesnysis /aukštasis išsilavinimas.


• Geros lietuvių kalbos žinios raštu/žodžiu;


• Gerai mokėti dirbti kompiuteriu (Outlook, MS Word, MS Excel)


• Geros anglų kalbos žinios raštu ir žodžiu;


• Lankstumas, sugebėjimas dirbti komandoje;


• Tikslumas bei dėmesys detalėms;


• Geri bendravimo įgūdžiai.

• Panašaus darbo patirtis


• Gebėjimas vienu metu dirbti su keliomis užduotimis;


• Kokybės valdymo sistemų pagrindų žinojimas;


• Intersurgical procesų ir produktų žinojimas;


• Patirtis medicinos prietaisų gamyboje.


• Techninių dokumentų skaitymas ir supratimas

• Įdomų ir iššūkių kupiną darbą pasaulinio lygio įmonėje;


• Apmokymus;


• Puikią galimybę lavinti įgūdžius ir patirtį;


• Draugišką darbo atmosferą;


• Atostogas laiku ir darbą be viršvalandžių;


• Transportavimą autobusais į ir iš darbo (Vilnius-Pabradė-Vilnius) esant poreikiui;


• Nemokamas sporto salės lankymas Pabradėje


• Darbo užmokestis 1500 – 1800 Eur/mėn. su mokesčiais (priklausomai nuo turimos patirties ir žinių).


• Metinis darbų įvertinimas ir atlyginimo peržiūra.

CHANGE CONTROL COORDINATOR (VILNIUS OFFICE)

To coordinate changes within organisation by using established project management methodology and IT systems.

Location: Vilnius office

Main Responsibilities

• Oversee Change Control process for organisation-wide changes.


• Participate in Change Control projects for timely and effective implementation.


• Coordinate with departments and sites for change control activities.


• Verify project implementation compliance with internal procedures.


• Conduct training on Change Control process.


• Organise project meetings and prepare minutes.

Essential Skills

• Higher education.


• Strong English documentation skills.


• Fluent in Lithuanian.

Desirable Skills

• Basic knowledge in project coordination and quality management.


• Ability to multitask and solve problems.


• Proactive and team-oriented.


• Effective communication skills.

Why should you apply?

• Engaging work in medical device industry.


• Comprehensive training.


• Skill development opportunities.


• Friendly environment.


• Timely holidays, no overtime.


• Competitive salary 1700 to 2200 Eur before taxes (dependent on background and experience).


• Annual appraisals.