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Pareigos Quality Compliance Specialist
Aprašymas To work in Quality and Regulatory department

Main responsibility:
Performing internal audits of the Quality System at Intersurgical manufacturing sites to ensure compliance with the established Company policy, procedures and applicable regulatory requirements. Conducting gap analysis afterwards to ensure that remedial actions are carried out. Organising and coordinating project activities.
Basic Qualifications:
  • 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 

Prefered Qualifications:
  • Documentation preparation skills
  • Internal auditors certificate  
We offer:
  • Interesting and challenging work
  • Competitive salary
  • Work in growing company
Confidentially is guaranteed. Please send your CV in English marked “Quality Compliance Specialist” by 26th of July to
Galioja iki 7/26/2019
Pasiūlyti savo kandidatūrą
Aprašymas To work in Quality and Regulatory

Job description:
  • Maintain manufacturing/laboratory equipment validation projects from an initiation to a closeout.
  • Identify and validate all manufacturing/laboratory equipment, which have impact on quality.
  • Develop and maintain qualification protocols, reports and other deliverables. 
  • Organize execution of tests according to developed qualification protocols.
  • Ensure initiation/preparation and closeout of all manufacturing/laboratory equipment validation related deviations.
  • Ensure that manufacturing/laboratory equipment validation status is maintained after release by performing a periodic and a non-periodic review and re-validation, where required.
  • Work in liaison with involved Intersurgical departments to ensure validation activities are completed in expected timelines. 

Main responsibilities:
  • Participation in manufacturing/laboratory equipment validation;
  • Coordination of qualification activities;
  • Generation of qualification documentation;
  • Always ensure quality issues are addressed and resolved.
Basic Qualifications:
  • Bachelor’s degree in Engineering or similar 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: MS Word, MS Excel, MS Outlook.
Preferred requirements and Qualifications:
  • Technical understanding of manufacturing and/or laboratory equipment.
We offer:
  • Interesting and challenging work;
  • Support and training;
  • Good work conditions and environment;
  • Competitive salary;
  • Free transport for employees from Vilnius.
Confidentially is guaranteed. Please send your CV marked “Equipment Validation Engineer” until the 17th of May, 2019 by
Galioja iki 8/31/2019
Pasiūlyti savo kandidatūrą
© UAB Intersurgical, 2019
Arnionių g. 60 Pabradė LT-18170 Lietuva
8 387 66611