Εμπόριο Λιανικής

Κατασκευαστικός Κλάδος / Τεχνικά Επαγγέλματα

Πληροφορική

Εστίαση

Αποθήκη / Logistics

Χρηματοοικονομικά

Βιομηχανική Παραγωγή

Εκπαίδευση

Τουρισμός / Ξενοδοχεία

Επαγγέλματα Υγείας

Άλλο

Εταιρικές Πωλήσεις

Αισθητική / Κομμωτήριο

Διοίκηση Επιχειρήσεων

Μεταφορές

Ναυτιλία

Γραμματειακή Υποστήριξη

Κέντρο Εξυπηρέτησης / Call Center

Ανθρώπινο Δυναμικό / HR

Προσωπικό Ασφαλείας

Φροντίδα Κτιρίων / Σπιτιών

Εργάτες

Marketing

Τέχνες / Πολιτισμός

Αερομεταφορές

ΜΜΕ / Social Media

Νομικές Υπηρεσίες

Φροντίδα Ενήλικων / Παιδιών

Αθλητισμός / Fitness

Τηλεπικοινωνίες

Φροντίδα Ζώων

Αγροτική Παραγωγή

LastWeek

LastThreeDays

Today

Aoristou

Seasonal

Orismenou

Internship

Volunteer

FullTime

PartTime

OnSite

Hybrid

Remote

What we basically need from you:<ul><li>Flexibility&nbsp;in handling queries &amp; requests of our young guests.</li><li>Proven &amp; Formal Certification Ability.</li><li>Friendly with Children.</li><li>Well command of the English language.</li></ul>&nbsp;&nbsp;What we offer to you:<ul><li>Modern &amp; professional environment.</li><li>Earnings package after agreement.</li><li>Benefits &amp; Bonus.</li><li>Accommodation &amp; meals.</li></ul>

CHILD CARE ESCORT / PEDAGOGUE

What we basically need from you:<ul><li>Proven Experience at similar position.</li><li>Good knowledge in handling queries &amp; requests.</li><li>Well command of English Language.</li><li>Efficiency &amp; effectiveness in all aspects.</li><li>Focusing on guests’ needs and demands.</li><li>Team spirit &amp; Team player.</li><li>Well knowledge of the Hotel cluster and the island.</li></ul>What we offer to you:<ul><li>Modern &amp; Professional working environment.</li><li>Earnings package after agreement.</li><li>Benefits &amp; Bonus.</li><li>Accommodation &amp; meals.</li><li>Window of moving up opportunity.</li></ul>

GUEST RELATIONS AGENT

What we basically need from you:<ul><li>Basic Experience at similar position.</li><li>Good knowledge in handling queries &amp; requests.</li><li>Basic knowledge of alcohol beverages and mixtures.</li><li>Focusing on guests’ needs and demands.</li><li>Team spirit &amp; Team player.</li><li>Well command of the English language.</li></ul>&nbsp;&nbsp;What we offer to you:<ul><li>Modern &amp; professional working environment.</li><li>Earnings package after agreement.</li><li>Benefits &amp; Bonus.</li><li>Accommodation &amp; meals.</li><li>Window of moving up opportunity.</li></ul>

BARISTA

<ul><li>What we basically need from you:Proven experience at similar position.</li><li>Well command of the English language.</li><li>P/C skills.</li><li>Administration for online systems, Internet channels, software &amp; hardware solutions.</li><li>Team player &amp; Team member.</li><li>Well knowledge of modern technologies.</li><li>What we offer to you:Modern &amp; professional working environment.</li><li>Earnings package after agreement.</li><li>Benefits &amp; Bonus.</li><li>Accommodation &amp; meals.</li><li>Window of moving up opportunity.</li></ul>

IT SUPPORT

<ul><li>What we basically need from you:Proven Experience at similar position.</li><li>Proven knowledge in handling queries &amp; requests.</li><li>Internet &amp; Social Media skills.</li><li>Good knowledge of Hotel Indexes, Quality ratio performances, Revenue statistics.</li><li>Perfect command of English Language.</li><li>Efficiency &amp; effectiveness in all aspects both quantity and quality oriented.</li><li>Focusing on guests’ needs and demands.</li><li>Team spirit &amp; Team player.</li><li>Well knowledge of the Hotel cluster and the island.</li><li>What we offer to you:Modern &amp; Professional working environment.</li><li>Earnings package after agreement.</li><li>Benefits &amp; Bonus.</li><li>Accommodation &amp; meals.</li><li>Window of moving up opportunity.</li></ul>

GUEST RELATIONS MANAGER

What we basically need from you:<ul><li>Proven Experience at similar position.</li><li>Proven knowledge in handling queries &amp; requests.</li><li>Internet &amp; Social Media skills.</li><li>Skills in conducting technical duties, i.e. Shift change, check in – out procedure, billing procedure, tasks delegation, reporting, revenue &amp; cost control.</li><li>Perfect command of English Language.</li><li>Efficiency &amp; effectiveness in all aspects both quantity and quality oriented.</li><li>Focusing on guests’ needs and demands.</li><li>Team spirit &amp; Team player.</li></ul>What we offer to you:<ul><li>Modern &amp; Professional working environment.</li><li>Earnings package after agreement.</li><li>Benefits &amp; Bonus.</li><li>Accommodation &amp; meals.</li><li>Window of moving up opportunity.</li></ul>

FRONT OFFICE SHIFT SUPERVISOR

The Associate Medical Director perform the medical assessment activities related to drug safety pharmacovigilance for the assigned therapeutic area(s). The Associate Medical Director proactively evaluates safety information from individual cases and cumulative data, identifies and analyses potential signals, and communicates data-driven conclusions to internal and external stakeholders.The Associate Medical Director Reports to Therapeutic Area Head or to Medical Director.What You Will AchieveIn this role, you will:<ul><li>Perform single case medical assessment, including the determination of seriousness, expectedness/listedness/labeledness, and causality of adverse events in compliance with current regulations, internal and external guidance documents, Standard Operating Procedures, Safety Job Aids, the Argus User Reference Guide and case processing/coding</li><li>conventions.</li><li>Maintain the timely submission of expedited reports.</li><li>Support the achievement of the Therapeutic Area’s case processing performance timelines. Identify cases that meet SUSAR reporting criteria, prepare the SUSAR narrative, perform risk assessment, initiate the unblinding process (as appropriate), and make the report available for distribution.</li><li>Identify and evaluate safety signals based on individual cases and cumulative data assessment and by using other signal detection systems. Provide data-driven decisions and communicate these findings proactively and effectively to the key stakeholders.</li><li>Partner with Safety Surveillance and Risk Management and with other Worldwide Safety and Regulatory functional groups to monitor the safety profile of assigned products.</li><li>Actively participate in Risk Management Committees and other risk management activities for assigned therapeutic areas. Perform product safety reviews as appropriate.</li><li>Provide medical safety input as appropriate to Clinical Development Teams regarding expectedness/listedness/labeledness, causality, and data reconciliation.</li><li>As appropriate, provide medical safety input, and review or draft sections of response documents to health authority inquiries.</li><li>Work with the Therapeutic Area Head and Medical Review Head to proactively and effectively communicate product safety issues and proposed solutions to PSSR management and to the Office of the EU Qualified Person.</li><li>Provide timely review of and input to documents, including labeling, protocols, Investigator Brochure, and licensing agreements.</li><li>Provide timely input into product related milestones.</li><li>Provide medical input, review and analysis of Periodic Safety Update Reports, Expert Statements, Risk Management Plans, and other aggregate reports; where appropriate, draft components of these reports. Ensure accurate, relevant, and meaningful ICSR data and insights.</li><li>Provide medical advice and insights to Therapeutic Area colleagues to improve the quality, consistency, accuracy, and clinical relevance of safety reports.</li><li>Support PSSR Quality Assurance activities, addressing observations related to medical assessment, as appropriate. Ensure consistency and quality of the medical assessment process.</li><li>Provide drug safety support when appropriate to product acquisitions, recalls, and legal issues.</li><li>Take responsibility for inspection readiness for medical assessment activities; support regulatory authority inspections when needed.</li><li>Proactively communicate with and engage Therapeutic Area colleagues and key stakeholders (e.g., Clinical Development Teams, Regulatory Affairs, Licensing, Manufacturing, and Marketing) to support business objectives and to discuss and resolve safety issues.</li><li>Engage internal and external customers with a sense of urgency and an appreciation of their needs and point of view.</li><li>As an individual contributor, initiate and/or take a leadership role in projects/process improvements that align with PSSR strategic objectives.</li><li>Develop and maintain comprehensive and current knowledge (e.g., indications, labeling documents, pharmacology) for the assigned product portfolio.</li><li>Develop and maintain a comprehensive working knowledge of current regulations governing the processing and reporting of safety data, Standard Operating Procedures, Safety Job Aids, and case processing/coding conventions, consistently completing curriculum training by the specified due dates.</li><li>Utilize the corporate performance management process to manage goal setting and individual development. Consistently demonstrate Pfizer Values and Leader Behaviors.</li><li>Proactively mentor Therapeutic Area colleagues to foster an environment of trust, understanding, learning, and development.</li><li>Manage or contribute to the mentoring and on-boarding of new PSSR colleagues</li></ul>Here Is What You Need Technical Skill Requirements<ul><li>Demonstrated computer literacy, with proficiency in the use and management of safety databases, including the Pfizer Global Safety Database, Argus Safety, and MS Window, Excel, Word and Outlook</li><li>Ability to achieve personal objectives while meeting departmental standards of performance</li><li>Fluency in oral and written English; knowledge of additional language(s) an advantage</li><li>Experience and skill with medical writing an advantage</li></ul>Qualifications <ul><li>Medical Degree from an accredited institution</li><li>One to two years of experience as an MD in clinical practice</li><li>One to two years of relevant experience in pharmacovigilance, clinical research or related field</li><li>Pharmaceutical industry experience preferred</li><li>Working knowledge of international regulations and guidance documents as related to worldwide reporting requirements, preparation of clinical trial safety assessments, and regulatory submissions including the preparation of aggregate reports</li></ul>Please apply by sending your CV and a motivational letter in English

Associate Medical Director

Είστε έτοιμοι να γίνετε μέρος μιας δυναμικής ομάδας που διαδραματίζει καθοριστικό ρόλο στην αποδοτική λειτουργία της αποθήκης μας; Αναζητούμε έναν επαγγελματία που θα συνεργάζεται στενά με εσωτερικούς και εξωτερικούς συνεργάτες, προάγοντας πρωτοβουλίες για συνεχή βελτίωση και επιτυχία. Μια Μέρα στη Ζωή Σου<ul><li>Διαχείριση μετακίνησης και αποθήκευσης επαγγελματικών μηχανών εντός της αποθήκης</li><li>Συσκευασία, φόρτωση/εκφόρτωση κουτιών και παλετών, ταξινόμηση και οργάνωση πόρων</li><li>Χρήση εξοπλισμού (παλετοφόρο, ανυψωτικά) για εσωτερικές μεταφορές</li><li>Ακριβής καταγραφή και έλεγχος αποθέματος</li><li>Διαχείριση εγγράφων παραλαβής και αποστολής</li><li>Συνεργασία με τεχνικές ομάδες και εξωτερικούς συνεργάτες (μεταφορικές εταιρείες, τεχνικούς)</li><li>Διατήρηση καθαρού και οργανωμένου χώρου αποθήκης</li></ul>&nbsp;Τι Χρειάζεται για να Ξεχωρίσεις<ul><li>Πτυχίο στη Διοίκηση Επιχειρήσεων, Εφοδιαστική, Οικονομικά, Μηχανική ή συναφές πεδίο</li><li>Μεταπτυχιακό στην Εφοδιαστική (επιθυμητό)</li><li>Τουλάχιστον 2 χρόνια εμπειρίας στην Εφοδιαστική Αλυσίδα</li><li>Άριστη γνώση MS Office και SAP</li><li>Ικανότητες επικοινωνίας, εξυπηρέτησης και οργάνωσης</li><li>Δίπλωμα οδήγησης</li><li>Άριστη γνώση Ελληνικής και Αγγλικής γλώσσας</li></ul>

Υπάλληλος Αποθήκης, Nestlé Professional

Αναζητούμε υπάλληλο για εργασία στη γραμμή παραγωγής&nbsp;για να υποστηρίξει με τις ικανότητές του τη διαδικασία παραγωγής των προϊόντων του εργοστασίου, με στόχο την εξυπηρέτηση και ικανοποίηση των πελατών μας Αρμοδιότητες ρόλου:Βοηθητικές εργασίες στη γραμμή παραγωγής&nbsp;&nbsp;Επιθυμητά προσόντα:<ul><li>Πτυχιούχοι ΤΕΙ&nbsp;</li><li>Εμπειρία σε περιβάλλον παραγωγής&nbsp;</li><li>Γνώση λειτουργίας Η/Υ (MS Office)</li><li>Βασική γνώση της αγγλικής γλώσσας&nbsp;</li></ul> Η εταιρία προσφέρει:<ul><li>Οργανωμένο περιβάλλον εργασίας σε μία από της μεγαλύτερες πολυεθνικές εταιρείες καταναλωτικών αγαθών</li><li>Ομαδικό Πρόγραμμα Νοσοκομειακής και Εξωνοσοκομειακής Ιατροφαρμακευτικής Περίθαλψης</li><li>Δυνατότητα εκπαίδευσης και συνεχούς εξέλιξης</li></ul>

Υπάλληλος Παραγωγής

We are looking for a dynamic person to join our Factory team. In this role, you will be responsible to ensure availability of all Raw &amp; Packaging materials required to cover production plan, to perform also materials planning in a long-term horizon taking into consideration long term requirements and Warehouse constraints. All operational buyer activities have to be performed according to LVS principles and guidelines. &nbsp;Position snapshot Nestlé Coffee Factory, Oinofyta, Greece Reporting to: Supply Chain Factory Manager Contract: temporary assignment (12 months contract)&nbsp;A day in the life…<ul><li>Review long and short-term material requirements (ROH, pack, HALB) and act according to actual needs (make all necessary adjustments related with call offs)</li><li>Communication with suppliers for call offs, creation of PO's and for any other request related with factory operation</li><li>Communication with Procurement for creation and adjustment of contracts signed with all suppliers</li><li>Master Data of all materials update</li><li>Active involvement to production planning</li></ul>&nbsp;What makes you successful<ul><li>University Degree in Logistics/Statistics or any other related field</li><li>MBA or Master in Logistics or Statistics would be a plus</li><li>Preferably 1 year of experience in Supply Planning/Operations/Production Planning</li><li>Adaptable, agile, communicative, good team player, hard-working, able to work autonomously, with negotiation and convincing skills</li><li>Ability to prioritize job effectively and support multi-tasking activities is vital for successful performance</li><li>Proactive cooperation, initiative, results focus</li><li>SAP knowledge would be considered as an asset</li><li>Fluency in Greek &amp; English</li></ul>&nbsp;Why you should apply Enjoy the wide range of Nestlé benefits such as:<ul><li>competitive salary &amp; performance bonus</li><li>meal vouchers</li><li>comprehensive Pension, Health Care &amp; Life Insurance programs</li><li>increased Parental leaves for both caregivers and Baby Support plan</li><li>Flexible Work policy</li><li>Wellbeing and Recognition days off</li><li>“Bring Your Pet At Work” &amp; Pet Support plan</li><li>free car parking</li><li>in-house restaurant and mini market</li><li>participation to health and wellness activities and much more</li></ul>Join the leading Food &amp; Beverages company in the world with more than 93bio CHF sales and presence in 185 countries.&nbsp; Engage with our people from all over the world and join exciting local or international projects and assignments, constantly pushing boundaries Take full advantage of unlimited development opportunities through an extensive physical, virtual and hybrid learning ecosystem, both at local and international level

Factory Planner, 12month contract

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child care escort / pedagogue

ELIVI Skiathos

guest relations agent

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barista

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it support

ELIVI Skiathos

guest relations manager

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front office shift supervisor

ELIVI Skiathos

associate medical director

Pfizer Hellas

υπάλληλος αποθήκης, nestlé professional

Nestlé

υπάλληλος παραγωγής

Nestlé

factory planner, 12month contract

Nestlé