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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 moulding projects.
• Identification of critical moulding processes.
• Formation of multi-functional teams for planned activities.
• Preparation of protocols.
• Confirmation by objective evidence that moulding 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 1000 Eur before taxes (depends on background and experience).
• Timely holidays and no work overtime.
• Company’s transportation to/from work.

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Confidentially is guaranteed. Please send your CV marked “Validation Engineer” until the 9^th of February 2020 by info@intersurgical.lt

• High education
• Ability and skills to review documented regulatory requirements and assess compliance of the quality system with these regulations
• Planning and organisation skills
• High level of accuracy and attention to details
• Good interpersonal skills to work as part of a team
• Very good verbal and written English for audit reports
• Computer knowledge: MS Word 

• Documentation preparation skills
• Internal auditors certificate  

• Interesting and challenging work
• Salary from 1600 Euro (Bruto)

• To liaise with raw material suppliers;
• To introduce new materials in Intersurgical products;
• To organise injection moulding and extrusion trials;
• To manage component/product evaluations, data analysis;
• 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.
• To maintain these high standards the company is looking to work at its site in Pabradė.

• Bachelor’s degree in the fields of chemistry/Engineering/Physics;
• Job experience in chemistry/medical industry/quality area/project coordination;
• Planning, organizational and project management skills.

• Good English language skills (written and oral);
• Good computer and MS Office skills;
• Good problem solver with a hands-on approach;
• Good level of accuracy and attention to details;
• Good communication skills, ability to work both in a group and independently, thoroughness and diligence;
• Able to function effectively across a number of interrelated departments.

• Interesting work in an ever growing UAB “Intersurgical” company;
• Friendly environment and full training;
• Great opportunity to develop skills and experience;
• Company’s transportation to/from work.
• Salary from 1100Eur before taxes (depends on background and experience)
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