Laisvų darbo vietų sąrašas

To work in Quality and regulatory department
Role overview:
Validation engineers carry out essential quality functions to ensure that medical devices are safely and effectively produced for patients all over the world.
 
Key responsibilities:

• Management of validation projects.
• Identification of critical manufacturing equipment/processes.
• Formation of multi-functional teams for planned activities.
• Preparation of protocols.
• Confirmation by objective evidence that manufacturing equipment/processes are in compliance with EU and US requirements.

• Bachelor’s degree in Engineering or Technical discipline.
• Planning, organizational and project management skills.
• Verbal and written communication skills in English & Lithuanian.
• Ability to work and interact with various personnel.
• Computer knowledge: Microsoft Office.

• Basic understanding of international standards.
• Technical understanding of manufacturing equipment/processes.

• Interesting and challenging work.
• Learning, personal development and growth.
• Friendly environment.
• Salary from 1100 Eur before taxes (depends on background and experience).
• Timely holidays and no work overtime.
• Company’s transportation to/from work.

 ____________________________________________________________________________
Confidentially is guaranteed. Please send your CV marked “Validation Engineer” until the 10^th of March 2020 by info@intersurgical.lt

• Gamybinės įrangos/procesų, kuriems reikalingas atestavimas, identifikavimas.
• Atestavimo protokolų ir ataskaitų ruošimas.
• Veiksmų, pagal paruoštus atestavimo protokolus, atlikimas.

• Aukštasis arba aukštesnysis išsilavinimas (gali būti dar nebaigtas).
• Atsakingumas, kruopštumas, nuoseklumas.
• Anglų kalbos pagrindai.
• Darbas kompiuteriu: Microsoft Office.

• Patirtis gamybinėje įmonėje.
• Patirtis kokybės srityje.

• Įdomų ir atsakingą darbą tarptautinėje, nuolat augančioje įmonėje.
• Darbą draugiškoje aplinkoje, jauname kolektyve.
• Galimybę mokytis ir tobulėti.
• Darbo atlyginimą nuo 900 Eur iki mokesčių (priklausomai nuo išsilavinimo ir turimos patirties).
• Savalaikes atostogas ir jokių viršvalandžių.
• Įmonės transportą veržimui į/iš darbo.

• Playing one of the central roles within the Quality Management System by managing product and process corrective and preventive actions at corporate level
• Overseeing, monitoring and driving CAPA process
• Working as a part of Quality and Regulatory Affairs team, focusing on the continuous improvement of quality management system and its processes effectiveness and compliance
• Working in a cross-functional environment, including Manufacturing, Engineering, Technical, Product management and other teams, to address and resolve quality issues and to close gaps identified by audits
• Managing CAPA as projects from initiation to completion
• Managing CAPA coordination staff

• High education
• Exceptional written and oral communication skills in English and Lithuanian
• Good working with others and problem solving skills
• Proactivity and ability to learn
• Knowledge of Microsoft Office
• Ability to take leadership in a work
• Ability to motivate interested parties and work closely with them to determine best practices and acceptable solutions
• Good interpersonal skills to work collaboratively in a team environment 
  PREFERRED SKILLS OR EXPERIENCE
• Understanding of Quality Assurance systems
• Understanding of project management 

• Interesting and challenging work
• Friendly environment
• Timely holidays and no overtime
• Company’s transportation to/from work
• Salary from 3000 Eur before taxes (depends on background and experience)