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locuri de munca in Strainatate.

Pagina 1 din 1
Soferi de TIR In Comunitate
  • - Descrierea firmei Breen International/Darrastrans ltd este o firma de Logistica. Cu Sediul central in Irlanda. Ne ocupam cu transportul inrernational.

10 posturi disponibile (1 aplicant )

31-07-2015
Recrutam asistenti medicali
  • - Diploma de asistent medical /Nationalitate UE
    - Inregistrarea NMC inceputa sau finalizata
    - Un nivel bun de engleza
    - Motivare
    - Sentimentul de angajament ?i cuno?tin?e de îngrijire a persoanelor vârstnice
    - Experienta anterioara de asistent medical va fi apreciata!

50 posturi disponibile (0 aplicanti)

30-07-2015
Inginer Calitate /Inginer Validare
  • - Responsabilitati
    - Asigura suportul Circuitului de Productie
    - Ia legatura cu Departamentul de Reglementare pentru a se asigura ca productia se mentine la un anumit nivel si ca sunt indeplinite toate normele cu privire la calitatea produsului
    - 3
  • - 5 ani experienta ca si Inginer QA/ QE in domeniul fertilizarii IN VITRO a Dispozitivelor Medicale sau a Industriei Farmaceutice.
    - Conditii de recrutare:
    - 2
  • - 3 experienta in validarea de echipamente/producere/software este cerinta obligatorie
    - Cunostinte tehnice de fertilizare IN VITRO sau a Dispozitivelor Medicale constituie un avantaj

3 posturi disponibile (0 aplicanti)

30-07-2015
Manager Vanzari pentru Europa de Est si Orientul Mijlociu
  • - Responsabilitate in vanzari in cadrul pietelor de Hemoglobina, Boli Infectioase, Chimie Clinica, Produse de Ingrijire si Produse pentru boli autoimmune.
    - Responsabil/a pentru atingerea targetelor de vanzari regionale
    - Impreuna cu echipa de conducere propune si elaboreaza tehnici de crestere a vanzarii si atingerea targetelor propuse Diploma de licenta sau de master in domeniul stiintelor
    - Minium intre 3
  • - 5 ani experienta in vanzari prin
    - Experienta de HPLC si/sau HbA1c cu teste imunologice
    - Cunostine avansate de limba engleza. Cunostinte de alta limba straina constituie un avantaj
    - Experienta in domeniul vanzarii in Orientul Mijlociu sau in Europa de Est este un avantaj
    - Experienta si cunostinte in toate domeniile de Diagnostic in In Vitro de la R&D si a Normelor de Calitate si Comerciale

3 posturi disponibile (4 aplicanti)

29-07-2015
Specialist Quality Assurance /RA
  • - Respectarea Normelor Sistemului de Calitate FDA 21 CFR 820(QSR)
    - Respectarea Directivei de Diagnostic Medical In Vitro 98/79/EC
    - Respectarea Normelor de Sanatate canadiene
    - Respectarea Normelor Managementului Sistemului Medical ISO13485
    - Asista Managerul QS in Intretinerea Managementului Sistemului Calitatii
    - Asigura suportul pentru toate reglementarile si schimbarile propuse de departamentul Operational
    - Ia act de toate reglementarile cu privire la designul produsului si a echipei de redezvoltare R&D
    - Ofera tot suportul necesar echipei R&D in pregatirea DHF si a Cartii Tehnice pentru a se asigura ca produsul respecta toate normele in vigoare
    - Lider de echipa in pregatirea activitatii de inspectie FDA sau a altor audit
  • - uri ale clientului si audit
  • - uri de supraveghere conform ISO13485, urmarind indeaproape toate aceste activitati
    - Revizuirea reclamatiilor clientilor si Modificarea tehnicilor Controlului CAPA
    - Revizuirea permanenta a tehnicilor de productie in concordant cu normele international
    - Mentine si dezvolta CAPA si tendintele de dezvoltare ale acesteia
    - Efectuarea auditur
  • - ilor interne si ale furnizorilor in functie de necesitati
    - Proiecteaza si pune in aplicare tehnici de imbunatatire a sistemelor calitatii
    - Inregistrari globale pentru toate produsele etichetate
    - Activitati QA/RA pentru Republica Irlanda
  • - Filiala din Norvegia&Filiala din Marea Britanie
    - Suport pentru reglementarea la nivel mondial a tuturor produselor etichetate
    - 3 ani experienta in domeniul calitatii produsului in sectorul industriei farmaceutice, medicale, in industria fertilizarii IN VITRO( conditie obligatorie) sau intr
  • - un domeniu similar, constituie avantaj cunoasterea normelor FDA
    - Cunostinte ale sistemului managementul calitatii si a Normelor Internationale Europene cu privire la diagnosticul IN VITOR /dispozitive medicale

1 post disponibil (1 aplicant )

29-07-2015
Specialist Audit in Domeniul Fertilizarii IN VITRO
  • - Reprezentant ISO9001(ISO9000, 4.1.2.3, ISO 9001), ISO13485
    - Pregatirea si revizuirea in permanenta a Manualului de Calitate al produsului
    - Participarea la cursuri si training
  • - uri cu privire la toate standardele si reglementarile calitatii care au impact asupra industriei din sectorul IN Vitro
    - Organizarea Managementului Controlului Calitatii precum si compilarea si raportarea performantei sistemului de calitate
    - Se asigura ca toate cerintele specifice clientilor in ceea ce priveste calitatea sunt respectate in urma revizuirii contractului
    - Managementul Controlului Calitatii Produsului si a sistemului de emitere a Certificatului de Conformitate
    - Managementul modificarii Controlului si a Sistemului de Control al Documentelor
    - Emiterea, controlarea si depunerea tuturor documentelor legate de lotul de produse
    - Responsabil pentru toate semnaturile de iesire de pe etichetele produselor precum si pentru insertia coletelor si a materialelor de Marketing
    - Organizarea productiei si facilitarea inspectiei, pregatirea procedurilor si a instructiunilor care include evaluarea certificatelor si supravegherea auditului sau alte inspectii de reglementare si audit
  • - uri ale furnizorului
    - Se asigura ca echipamentele, procesele si software
  • - ul utilizat in procesul de fabricatie al produsului sunt valide
    - Managementul sistemelor de actiuni preventive si corective, inclusiv controlul produselor prelucrate ulterior si livrarea produselor neconforme sau in non
  • - conformitate sau ale caror conditii nesatisfacatoare au fost corectate
    - Responsabil pentru coordonarea si emiterea Notificarii de Siguranta a Produsului sau a Produsului Retras precum si Dispozitivul Medical de Reportare( MDR) impreuna cu Vice Presedintele Controlului Calitatii
    - Se asigura ca cele recente actualizari ale cerintelor de reglementare sunt puse in aplicare si disponibile pentru utilizare si comunicate departamentului
    - Se asigura de respectarea reglementarilor existente la nivel mondial/depunerea de reglementari
    - Participant cheie in controlul proiectarii
    - Asista Vice Presedintele Controlului Calitatii la depunerea de reglementari FDA
    - Comunica departamentului cerintele clientului si ia initiativa pentru imbunatatirea controlului calitatii
    - Asigura legatura cu partile externe pe problemele sistemului de management al calitatii
    - Se asigura ca toate procedurile privind sanatatea si securitatea la locul de munca sun respectate si ca societatea respecta legislatia in vigoare Studii in Domeniul Ingineriei Chimice
    - 5
  • - 7 ani experienta in domeniul industriei, trei ani experienta in industria fertilizarii IN VITRO sau intr
  • - un domeniu similar
    - Experienta in managementul proiectelor
    - Experienta in domeniul auditului
    - Experienta in conducerea de audit
  • - uri in domeniul FDA
    - Training
  • - uri in Sistemul Calitatii si in Sistemul Procesului de fabricare

3 posturi disponibile (1 aplicant )

29-07-2015
Sofer de TIR cu Experienta
  • - Atestat ADR (nu este obligatoriu dar constituie un avantaj) Card thachograf Cazier judiciar curat Limba engleza ( nu este obligatorie dar constituie avantaj) Minim 3
  • - 5 ani experienta

10 posturi disponibile (5 aplicanti)

28-07-2015
Telecom Technician (Rigger)
  • - Requirements:
  • - Minimum 3 years experience in telecom, especially with Ericsson equipment;
  • - Knowledge of equipment configuration using the software provided by Ericsson;
  • - Knowledge of acceptance testing, including using mobile devices;
  • - Knowledge of checking alarms in the system, their reporting and conducting remedial activities;
  • - Working at heights experience and certificate;
  • - Good level of English;
  • - Driving license
  • - B category;
  • - Communication skills and teamwork

5 posturi disponibile (1 aplicant )

27-07-2015
Soferi de TIR In Comunitate
  • - Atestat ADR(nu este obligatoriu dar constituie avantaj)
  • - Card tahograf
  • - Cazier judiciar curat
  • - Limba engleza la nivel basic ( fraze si vocabular legat de meserie)
  • - experienta minim 6
  • - 12 luni pe tiruri de 40 t

10 posturi disponibile (12 aplicanti)

20-07-2015
Centru de ingrijire din republica irlanda angajeaza asist...
  • - Conditii impuse de Angajator: Obligatoriu :intre 3 luni
  • - 12 luni de experienta Cunostinte avansat de limba engleza scris si vorbit Inregistrare la An Bord Altranais / In curs de inregistrare la An Bord Altranais, www.nursingboard.ie Fara abateri de la lege sau sanctiuni la locul de munca Ce trebuie sa stiti? NU PRECEPEM COMISION SAU TARIF DE MEDIERE PENTRU GASIREA UNUI LOC DE MUNCA

13 posturi disponibile (0 aplicanti)

20-07-2015

19 joburi care ti se potrivesc au fost publicate in aceasta saptamana

  • Alege sa primesti pe e-mail cele mai bune joburi.
Software Testing Engineer
  • - System software testing. System modeling. Writing reports. Testing of individual components of the system Simulation of the system Experience from 3 years; Desirable C/C++ knowledge. Version control system (SVN or another); Task tracking system (Redmine or another); High motivation level

1 post disponibil (0 aplicanti)

17-07-2015
Software engineer (C/C++) (QT, openGL)
  • - Development of the warehouse visualization software. Development of the Warehouse IDE. Development of new and improve existing code. Programming experience from 5 years; C/C++ knowledge (gcc, Ms VS), object oriented programming; Multithreading; POSIX; STL, Boost (ASIO, smart pointer, serialize); Network (TCP/IP); SQL; XML; Version control system (SVN or another); Task tracking system (Redmine or another); High motivation level

1 post disponibil (0 aplicanti)

17-07-2015
Software engineer (C/C++) (server)
  • - Development of Robot material handling system. Development of new and improve existing code. Programming experience from 5 years. Crossplatform software development; C/C++ knowledge (gcc, Ms VS), object oriented programming; Multithreading; POSIX; STL, Boost (ASIO, smart pointer, serialize); Network (TCP/IP); SQL; XML; Version control system (SVN or another) Task tracking system (Redmine or another) High motivation level

1 post disponibil (2 aplicanti)

17-07-2015
Software engineer (C/C++) (Robot logic)
  • - Development of the robot control software. Motion algorithms, routing, connection with the server and its neighboring robots. A software emulator for the robot. Development of new and improve existing code. Programming experience from 5 years; C/C++ knowledge (gcc), object oriented programming; QNX RTOS; Multithreading; POSIX; STL, Boost (ASIO, smart pointer, serialize); Network (TCP/IP); SQL; XML; Version control system (SVN or another); Task tracking system (Redmine or another); High motivation level

1 post disponibil (1 aplicant )

17-07-2015
Senior software engineer (C/C++) (Robot motion control)
  • - Software development of the control of the active robot equipment (QNX 6, drives MaxonMotor, DunkerMotoren, Pepperl+Fuchs technical vision modules, power controller, scanners and sensors). Robot motion control, positioning, path correction. Development of new and improve existing code. Programming experience from 5 years; C/C++ knowledge (gcc), object oriented programming; QNX RTOS; Multithreading; POSIX; STL, Boost (ASIO, smart pointer, serialize); Network (TCP/IP); SQL; XML Fieldbus CAN/CANopen; Version control system (SVN or another); Task tracking system (Redmine or another); High motivation level

1 post disponibil (1 aplicant )

17-07-2015
Senior software engineer (C/C++) (server)
  • - Development of Robot material handling system. Design of a network data exchange protocol for system components. Development of new and improve existing code. Programming experience from 5 years. Crossplatform software development; Skills in the software architecture design C/C++ knowledge (gcc, Ms VS), object oriented programming; Multithreading; POSIX; STL, Boost (ASIO, smart pointer, serialize); Network (TCP/IP); SQL; XML; Version control system (SVN or another) Task tracking system (Redmine or another) High motivation level

1 post disponibil (1 aplicant )

17-07-2015
Senior software engineer (C/C++) (Robot logic)
  • - Development of the robot control software. Motion algorithms, routing, connection with the server and its neighboring robots. A software emulator for the robot. Development of new and improve existing code. Programming experience from 5 years; C/C++ knowledge (gcc), object oriented programming; QNX RTOS; Multithreading; POSIX; STL, Boost (ASIO, smart pointer, serialize); Network (TCP/IP); SQL; XML; Version control system (SVN or another); Task tracking system (Redmine or another); High motivation level

1 post disponibil (0 aplicanti)

17-07-2015
Head of Quality Assurance and Regulatory Affairs
  • - Key member of the Operations Management Team and Corporate Quality Team.
    - ISO9001 Management representative (ISO9000, 4.1.2.3, ISO 9001, 5.5.2), ISO 13485.
    - Keep up to date of current Quality Standards and Regulations impacting the IVD industry.
    - Control of the Quality Manual including preparation, revision and execution.
    - Responsible for organising Management Review and compiling and reporting on the performance of the quality system.
    - Ensuring that all customer specific quality requirements are compiled with following contract review.
    - Management of the product review and release system and signature on Certificates of Conformity.
    - Management of Change Control and Document Control Systems.
    - Issuing, control and filing of all batch related documentation.
    - Responsible for final sign
  • - off on all product labels, package inserts and Marketing Material.
    - The organisation of product and facility inspection, preparation of procedures and instructions including certification assessment and surveillance audits, FDA inspections, other regulatory inspections and supplier audits.
    - Ensuring that validations are performed on equipment, processes and software used in manufacturing and testing of product.
    - The Management of non
  • - conformance and corrective and preventative action systems including the control of further processing and delivery of non
  • - conforming product until any deficiencies or unsatisfactory conditions have been corrected.
    - Responsible for coordination of issuing Product Safety Notifications or Product Recalls as well as Medical Device Reporting (MDR) with the Vice President of Regulatory Affairs.
    - Ensure latest updates of regulatory requirements are implemented and available for use and communicated to other facilities in the Trinity
    - Ensuring Compliance with worldwide regulations/ regulatory submissions.
    - Key participant in design control.
    - Assist with FDA regulatory submissions with the Vice President of Regulatory Affairs.
    - To communicate the awareness of customer requirements throughout the organisation and to champion Quality and continuous improvement initiatives.
    - To liase with external parties on matters of the quality management system.
    - Ensure that Health and Safety procedures are adhered to at all times and that the company ensures that at a minimum all legislative requirements are adhered to.
    - Primary degree qualification in a science, engineering or business discipline or equivalent in terms of relevant operational experience
    - 5
  • - 7 years + industrial experience, three years or more in the IVD industry or similar industry is required.
    - Must have experience in project management of change programs
    - First hand experience of audits by regulatory authorities.
    - Experience in hosting and leading FDA and other regulatory authority audits, would be an advantage.
    - Extensive experience of developing and delivering effective training on Quality Systems and Processes
    - Demonstrated track record and success in team building skills
    - Demonstrated experience of people management
    - A logical and planned approach to all tasks
    - An excellent communication skills, (both written and verbal), excellent interpersonal and presentation skills and be team focused.
    - An in
  • - depth knowledge of International Standards, GLP, and GMP
    - Ability to manage complex projects involving multiple functions
    - Ability to gain consensus on key quality/operational decisions.
    - Strong analysis/problem solving skills
    - Strong attention to detail/quality focus
    - Balanced cost/quality/customer focus
    - Willingness and ability to collaborate with and influence other groups in a positive, team
  • - based environment. Must also be able to hold others to account as required.
    - Work with a sense of urgency and have the ability to be impartial and objective.
    - Be an active learner and developer of self

3 posturi disponibile (2 aplicanti)

17-07-2015
URGENT Bone pentru diferite familii din Anglia.
  • - Selectam BONE pentru familii din Anglia sau Irlanda. Avantaje:
  • - Contract de colaborare pe min. 6 luni, familiile prefera pe 1 an
  • - Plecari rapide
  • - Banii castigati se pot economisii intrucat cazarea si mancarea sunt asigurate
  • - Nu este obligatorie experienta, sa vorbesti limba engleza sau sa ai permis de conducere
  • - Salarizarea
  • - intre 120
  • - 200 LIRE (720
  • - 1200 RON) / saptamana (remuneratia se plateste saptamanal si difera in functie de experienta candidatului, nivelul limbii engleze si daca are sau nu permis de conducere)
  • - Sunt posibile si cresterile salariale dupa o perioada de lucru.

5 posturi disponibile (2 aplicanti)

08-07-2015

19 joburi care ti se potrivesc au fost publicate in aceasta saptamana

  • Alege sa primesti pe e-mail cele mai bune joburi.
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