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HELLENIC CABLES&nbsp;is seeking&nbsp;a&nbsp;Project Technical Engineer&nbsp;to join Project Technical Department. As a&nbsp;Project Technical Engineer, you will be a highly trained engineer with a proven history of involvement in various technical projects (e.g. in construction/ manufacturing/ site supervision &amp; commissioning).Moreover, you will need to have great ability to cooperate with multi-disciplinary teams, a solid technical background, as well as the responsibility for maintaining Hellenic Cables standard of excellence and delivering projects with the utmost attention to safety and quality.Responsibilities:Provide technical support for various ongoing projects:<ul><li>Work Method Statements</li><li>New Technical Concepts</li><li>Technical Queries</li><li>Review of (sub-)contractor's technical documentation</li></ul>Provide technical support to installation teams:<ul><li>Cooperate on various cable/ accessories mock ups</li><li>Troubleshooting for issues occurring at projects during the implementation phase</li></ul>Cooperate and contribute to various technical/ project issues with:<ul><li>Tendering, Supply Chain, Engineering, Quality Control &amp; HSE Departments</li></ul>Provide project specific studies for the project implementation phase:<ul><li>Identification of technical risks and propose mitigation measures</li><li>In house developed technical solutions within deadlines</li></ul>Qualifications:<ul><li>Master Degree in Electrical, Mechanical or Civil Engineering</li><li>Minimum 2 years relevant working experience in industry (preferably offshore/ construction/ manufacturing/ site supervision &amp; commissioning)</li><li>Experience using CAD applications e.g. AutoCAD or SolidWorks will be considered an asset</li><li>Excellent communication, teamwork and interpersonal skills</li><li>Candidate must have excellent attention to detail and Technical Writing skills in both English &amp; Greek</li><li>Highly energetic, motivated and self-starter</li><li>Strong organization skills to prioritize workload</li></ul>The Company Offers:<ul><li>A unique opportunity to thrive in one of the pioneering companies in cable manufacturing</li><li>Competitive remuneration package</li><li>Life &amp; Health Insurance Plan</li><li>Additional Bonus, based on results</li></ul>

PROJECT TECHNICAL ENGINEER (2998)

Rontis Hellas SA, a Greek multinational healthcare company, active in the field of specialty healthcare (R&amp;D, production, international promotion and distribution of pharmaceuticals &amp; medical devices), is seeking to employ a highly skilled and hands-on:Production Engineer, Medical Devices&nbsp;The Production Engineer is responsible for implementing all necessary actions for the medical devices’ production, ensuring alignment with the standard operating procedures (SOPs), as well as complying with the quality procedures of the department to meet the necessary quality standards, customers’ expectations and regulatory requirements.Key responsibilities :<ul><li>Coordinates the production of medical devices in cooperation with the R&amp;D &amp; Production Director.</li><li>Controls and inspects all the production activities. &nbsp;Designs, modifies, and improves manufacturing processes (within guidelines) to increase productivity and efficiency.</li><li>Creates and overlooks production plans and schedules to ensure timely and cost-effective output.</li><li>Oversees the production personnel during production activities’ performance. Oversees the quality controls implemented by production personnel as indicated from work instructions.</li><li>Identifies and resolves issues that arise in the production process, including machinery malfunctions and process inefficiencies. Leads the trouble shooting and problem-solving actions. Communicates with the R&amp;D &amp; Production Director for problems/issues occurred during the production.</li><li>Adjusts the production machinery according to manufacturer’s instructions and machinery manual and in internal alignment with the R&amp;D &amp; Production Director.</li><li>Ensures adequate controls are in place for the timely adjustment of equipment and production systems, identifies malfunctions and then either initiates actions for their restoration or cooperates closely with the technical department for their repair.</li><li>Suggests proposals for improvements or for maintenance actions.</li><li>Ensures health and safety measures are respected by production personnel and that all production processes comply with safety regulations and standards.</li><li>Ensures timely training of production personnel on new or improved operating procedures and safety guidelines.</li></ul>Qualifications / Required skills:<ul><li>Degree of Technical Institute, Mechanical Engineering, Electrical Engineering, Electronics, Chemical Technology, Biotechnology or respective science.</li><li>Prior experience in the wider pharmaceutical or medical device field will be considered a plus., specifically in engineering roles. Prior experience in catheters’ production and assembly will be considered a major plus</li><li>Solid knowledge and understanding of ISO standards, GMP, MD regulation and compliance requirements</li><li>Strong problem-solving, investigative, and analytical skills</li><li>Ability to prioritize and handle multiple tasks, projects, and deadlines in a high-compliance environment&nbsp;</li><li>Excellent communication abilities, in both Greek &amp; English language.</li></ul>

Production Engineer, Medical Devices

DS Smith, a leading international sustainable packaging company, is seeking candidate to fill the position of Quality AnalystJob Summary&nbsp;Purpose of Role &nbsp;<ul><li>To deliver day to day execution of a segment of the Sites Operational activities, &nbsp;reporting to the Cluster Quality Manager. The specific accountabilities will be defined locally, based on the specific site needs, size and required number of employees covering these activities.</li><li>Quality improvement</li><li>Product Safety</li><li>Compliance vs standards &amp; regulations</li><li>Sustainability</li></ul>Key Accountabilities &amp;&nbsp;Main Responsibilities&nbsp;Quality assurance<ul><li>Act as principal point of contact for product/service quality and hygiene issues, for both Customer and internally raised matters · Administer customer complaints system including launching complaints, customer replies and monitoring of general efficiency of system, particularly complaint turnaround times. Brings the voice of the customer for product quality.&nbsp;</li><li>Lead/assist with investigations as required, using structured problem-solving techniques/cross functional teams where appropriate. Act promptly to prevent re-occurring issues through CAPA processes.&nbsp;</li><li>Provide relevant quality/technical data as required, including Quality Dashboard, and to ensure that all relevant noticeboards are maintained with current information.</li><li>Works closely with the site management team.&nbsp;&nbsp;</li><li>Conduct routine audits to ensure compliance, identification of non-compliance with appropriate corrective and preventative action. Implementation of opportunities for improvement and best practice.</li><li>Involved in customer visits.</li><li>Responsible for compliance standards and maintaining external certification.&nbsp;</li><li>Manage Sustainability topics like EUDR &amp; ESG</li></ul>Compliance<ul><li>To manage a timetable of checks and audits for the site.&nbsp; Ensure checks and documentation is taking place according to schedule.</li><li>To monitor and maintain validity of site certifications and their subsequent renewals.</li><li>To support SMI for customers in quality related matters</li><li>To administrate the provision and accuracy of production documents (Control sheets).</li><li>To identify problems and improvements with shop floor documentation by identifying non-compliance and working with operators to define improvements.</li><li>To undertake routine administration tasks related to compliant production.</li><li>To highlight non-compliance and work with managers on corrective action.</li></ul>Core Competencies&nbsp;Qualities/Attributes &nbsp;Job Specific Technical Requirements<ul><li>Must have experience of quality systems and root cause analysis.</li><li>Must have good analytical and good communications skills.</li><li>High level of rigour and organisation skills.</li><li>High level of Office Suite</li><li>Specific experience with Sustainability related topics</li><li>Numerate and able to conduct and present data analysis</li></ul>Desirable Qualifications &amp; Experience &nbsp;Evidenced &nbsp;<ul><li>Quality management experience &amp; qualifications (e.g. HACCP, Food Safety, BRC…)</li><li>Must be ISO lead auditor qualified.</li><li>Experience of working in Corrugated manufacturing environment.</li></ul>

Quality Analyst

Η ALPLA Pharma αναζητά GMP Responsible, ο/η οποίος/α θα έχει την ευθύνη για τη διασφάλιση της συμμόρφωσης των διαδικασιών παραγωγής με τις απαιτήσεις των Ορθών Πρακτικών Παραγωγής (GMP). Ο ρόλος απαιτεί οργανωτικότητα, προσοχή στη λεπτομέρεια και ικανότητα συντονισμού διαφορετικών λειτουργιών που σχετίζονται με την ποιότητα, την καθαρότητα και την ορθή τεκμηρίωση των δραστηριοτήτων στον Καθαρό Χώρο και την Ελεγχόμενη Περιοχή.Αν θέλεις να γίνεις μέλος&nbsp; μίας δυναμικής&nbsp; ομάδας, στείλε μας το βιογραφικό σου.<ul><li>Εποπτεία των διαδικασιών παραγωγής και αποστείρωσης για τη διασφάλιση της συμμόρφωσης με τα πρότυπα GMP.</li><li>Έλεγχο και απελευθέρωση προϊόντων βάσει προδιαγραφών GMP.</li><li>Εφαρμογή και διατήρηση συστημάτων διαχείρισης ποιότητας.</li><li>Εκπαίδευση και αξιολόγηση προσωπικού σχετικά με τις αρχές GMP.</li><li>Επιθεώρηση των εγκαταστάσεων και των διαδικασιών για την αποφυγή λαθών και παρατυπιών.</li><li>Καταγραφή και διαχείριση ποιοτικών θεμάτων που προκύπτουν κατά τη διάρκεια της παραγωγής.</li><li>Συντονισμό ενεργειών καθαριότητας και διακριβώσεων, διασφαλίζοντας την τήρηση των προγραμμάτων.</li><li>Επικοινωνία και συνεργασία με τα τμήματα Συντήρησης, Ποιοτικού Ελέγχου και Παραγωγής για την άμεση επίλυση τεχνικών ή ποιοτικών θεμάτων.</li><li>Διαχείριση και παρακολούθηση αποστολής δειγμάτων για μικροβιολογικούς, φυσικοχημικούς και ελέγχους στειρότητας.</li><li>Οργάνωση και τεκμηρίωση των διαδικασιών Validation (για εξοπλισμό και καλούπια) και Requalification (για τον καθαρό χώρο).</li><li>Έλεγχο και ενημέρωση αρχείων παρακολούθησης (θερμοκρασίας, υγρασίας, σωματιδίων).</li><li>Σύνταξη, αναθεώρηση και επικαιροποίηση διαδικασιών (SOPs), καθώς και διαχείριση μη συμμορφώσεων και corrective actions.</li><li>Συμμετοχή σε εσωτερικά και εξωτερικά GMP audits και υποστήριξη ενεργειών συμμόρφωσης.</li><li>Διαχείριση παραγγελιών αναλωσίμων και υλικών καθαρισμού για τη διατήρηση της εύρυθμης λειτουργίας του χώρου.</li></ul>What makes you great<ul><li>Πτυχίο θετικής κατεύθυνσης</li><li>Εμπειρία σε περιβάλλον παραγωγής υπό καθεστώς GMP (τουλάχιστον 1-2 έτη).</li><li>Καλή γνώση GMP, SOPs και αρχών ποιοτικού ελέγχου.</li><li>Ικανότητα τήρησης διαδικασιών και διαχείρισης τεκμηρίωσης.</li><li>Καλή γνώση MS Office</li><li>Ικανότητα ομαδικής εργασίας και επικοινωνίας με πολλαπλά τμήματα.</li><li>Καλή γνώση Αγγλικών (γραπτά &amp; προφορικά).</li></ul>What you can expect working with us<ul><li>Ανταγωνιστικό πακέτο αποδοχών, ανάλογα με την εμπειρία και τα προσόντα</li><li>Παροχές σε είδος με βάση την πολιτική της εταιρείας</li><li>Εταιρικά προγράμματα εκπαίδευσης</li><li>Εξισορροπημένο ωράριο με σεβασμό στην επαγγελματική και προσωπική ζωή</li></ul>

GMP Responsible

Ο/Η Quality Assurance Administrator θα αναφέρεται στον Manager του Τμήμα Ποιότητας και θα υποστηρίζει την διαχείριση των συστημάτων ποιότητας καθώς και την τήρηση των κανονιστικών απαιτήσεων (GMP/GDP). Διασφαλίζοντας την ορθή αρχειοθέτηση εγγράφων, τη συμμόρφωση με τις διαδικασίες και τη σωστή ροή πληροφοριών εντός του οργανισμού.&nbsp;Βασικές Αρμοδιότητες:&nbsp;<ol><li>&nbsp;Διαχειρίζεται και&nbsp; διεκπεραιώνει θέματα διασφάλισης ποιότητας σε συνεργασία με τους officers / managers του τμήματος.</li><li>Διαχειρίζεται το σύστημα διαδικασιών/εγγράφων, π.χ. Διαδικασίες γραμμής,&nbsp; ελέγχου, έγγραφα Validation, κλπ.</li><li>Συμμετέχει στην εφαρμογή του προγράμματος εσωτερικού ελέγχου και πραγματοποιεί flash inspections σαν εσωτερικός επιθεωρητής.</li><li>Συμμετέχει στην προετοιμασία για επιθεωρήσεις από πελάτες.</li><li>Συμμετέχει στην εκτέλεση του προγράμματος εκπαιδεύσεων GMP και στην εκπαίδευση του προσωπικού σύμφωνα με τις διαδικασίες του εργοστασίου ενώ βοηθάει στο συντονισμό του ετήσιου πλάνου εκπαίδευσης.</li><li>Παρακολουθεί την βάση δεδομένων των προληπτικών και διορθωτικών ενεργειών που προκύπτουν από τις διερευνήσεις, το χειρισμό των παραπόνων, των εγκεκριμένων αλλαγών και των επιθεωρήσεων εσωτερικών, πελατών, ΕΟΦ.</li><li>Συμμετέχει στην έκδοση του Validation Master Plan κάθε έτους, καθώς και των αντίστοιχων follow up.</li><li>Εκδίδει τα change controls που άπτονται του QS τμήματος.</li><li>Επικοινωνεί με προμηθευτές (υλών &amp; υλικών) σχετικά με αναφερόμενες ποιοτικές αποκλίσεις.</li><li>Συμμετέχει στην υλοποίηση του προγράμματος αξιολόγησης προμηθευτών.</li><li>&nbsp;Εκδίδει ή συμμετέχει στην έκδοση του Non Validation Master Plan κάθε έτους, καθώς και των αντίστοιχων follow up.</li></ol>&nbsp;Απαραίτητα Προσόντα:&nbsp;1.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Πτυχίο σε Φαρμακευτική, Χημεία, Βιολογία, Χημική Μηχανική, ή άλλο συναφές επιστημονικό αντικείμενο.2.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 1–3 χρόνια εμπειρία σε Quality Assurance ή συναφή ρυθμιζόμενο τομέα (φαρμακευτική, τρόφιμα, ιατροτεχνολογικά).3.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Πολύ καλή γνώση των GMP/GDP και βασικών αρχών ποιότητας.4.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Εμπειρία σε διαχείριση SOPs, CAPA, deviations, change control.5.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Άριστη χρήση MS Office (ιδίως Excel &amp; Word).6.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Πολύ καλή γνώση Αγγλικών, γραπτών και προφορικών.7.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ικανότητα χειρισμού ηλεκτρονικών συστημάτων ποιότητας θεωρείται πλεονέκτημα.

Quality Assurance Administrator

The Sr R&amp;D Compliance Officer will report to the R&amp;D Compliance Manager and will be responsible for documenting and monitoring the implementation of the Quality Assurance System, with the aim of ensuring product quality and achieving the objectives of the Department. The role requires strong coordination and communication skills with both internal departments and external partners/suppliers, ensuring compliance with applicable regulatory requirements (GMP, ISO, etc.).The position includes responsibilities covering the entire R&amp;D Department (Analytical/Formulation, CMC), as it will support both manufacturing sites (Pikermi &amp; Keratea).&nbsp;Responsibilities:·&nbsp;&nbsp;&nbsp;&nbsp; Drafting, reviewing, and revising procedures and SOPs related to the Department·&nbsp;&nbsp;&nbsp;&nbsp; Participation in the implementation of new systems and programs (or projects) related to product quality·&nbsp;&nbsp;&nbsp;&nbsp; Management of deviations and change controls·&nbsp;&nbsp;&nbsp;&nbsp; Preparation, issuance, and monitoring of the implementation/execution of corrective and/or preventive action plans (CAPAs)·&nbsp;&nbsp;&nbsp;&nbsp; Coordination and documentation of Cleaning Validation studies·&nbsp;&nbsp;&nbsp;&nbsp; Implementation of the personnel training process·&nbsp;&nbsp;&nbsp;&nbsp; Monitoring the implementation of the Validation Master Plan·&nbsp;&nbsp;&nbsp;&nbsp; Audit preparation and conducting internal audits·&nbsp;&nbsp;&nbsp;&nbsp; Submission of proposals to improve the Department’s operations·&nbsp;&nbsp;&nbsp;&nbsp; Collaboration with involved departments for the implementation of the Quality Management System (QMS) procedures·&nbsp;&nbsp;&nbsp;&nbsp; Responsibility for compliance with Health and Safety rules, in accordance with applicable legislation&nbsp;Technical Skills:·&nbsp;&nbsp;&nbsp;&nbsp; Knowledge of &nbsp;GMP's, Health and Safety requirements·&nbsp;&nbsp;&nbsp;&nbsp; Ability to write and review Procedures / Policies / Files / Instructions / Certificates / Protocols·&nbsp;&nbsp;&nbsp;&nbsp; Languages·&nbsp;&nbsp;&nbsp;&nbsp; Software Tools (Microsoft, QMS)·&nbsp;&nbsp;&nbsp;&nbsp; Audit Management Skills&nbsp;Required Qualifications/:·&nbsp;&nbsp;&nbsp;&nbsp; University Degree in Chemistry, Pharmacy, or in a relevant scientific discipline·&nbsp;&nbsp;&nbsp;&nbsp; At least 2 years of experience in a similar role·&nbsp;&nbsp;&nbsp;&nbsp; Fluent in English and Greek·&nbsp;&nbsp;&nbsp;&nbsp; Advanced computer skills (PC literacy)·&nbsp;&nbsp;&nbsp;&nbsp; Strong organizational and time-management skills·&nbsp;&nbsp;&nbsp;&nbsp; Team spirit and effective communication skills·&nbsp;&nbsp;&nbsp;&nbsp; Strong sense of responsibility with excellent attention to detail·&nbsp;&nbsp;&nbsp;&nbsp; FDA/ Anvisa experience will be considered as an asset

Senior R&D Compliance Officer

The position reports to the Packaging Manager and will be responsible for providing effective management and supervision to the Packaging operation to support company’s strategic goals and objectives.<ul><li>Supervise Packaging operation in Can Line to ensure high quality and effective production</li><li>Manage the department KPIs</li><li>Ensure compliance with HSE, food safety, hygiene and legal requirements</li><li>Ensure standardised problem-solving methodologies are used to resolve day to day problems</li><li>Develop direct reports to ensure thorough understanding of packaging technology and effective process control</li></ul>What we are looking for:<ul><li>University Degree in Mechanical or Chemical Engineering. MSc will be considered as an asset</li><li>At least 3 years of experience in production preferably in Food &amp; Beverage Industry aτ supervisory level</li><li>Lean experience will be considered as an asset</li><li>Fluency in Greek &amp; Proficient in English</li><li>MS Office (Word, Excel, PowerPoint)</li><li>SAP knowledge will be considered as an asset</li><li>Strong analytical and organizational skills</li><li>Structured personality distinguished quick-thinking and decision-making capabilities</li></ul>What you can expect from usWe foster an open communication and feedback culture in order to deal with our daily challenges. In addition to this, we also offer;<ul><li>Competitive remuneration package</li><li>Continuous Training&nbsp;</li><li>Opportunities for development</li></ul>

Packaging Leader (Σίνδος)

The&nbsp;Copper Tubes Division of ElvalHalcor&nbsp;is searching for a results-driven Product Design &amp; Customer Support Engineer, responsible for the design and supervision of new product development and production methods, to join our Development Department at Oinofyta, Voiotia, Greece.Role DescriptionKey Responsibilities:&nbsp; • &nbsp; &nbsp;Respond to customer technical inquiries regarding high-performance products, including production feasibility, availability of routings and production tools, and existing codifications. • &nbsp; &nbsp;Create and issue new production specifications for high-performance products and ensure adherence to these specifications. • &nbsp; &nbsp;Maintain and update the Specifications Library. • &nbsp; &nbsp;Manage product codifications, as well as the creation, maintenance, and updating of routings and Bills of Materials (BOM). • &nbsp; &nbsp;Handle and prepare samples and trial orders. • &nbsp; &nbsp;Provide customer service support (CTS) for issues related to high-performance products. • &nbsp; &nbsp;Coordinate development of new products (NPD Coordinator). • &nbsp; &nbsp;Design and optimize production processes for new products.&nbsp;Requirements:&nbsp; • &nbsp; &nbsp;Bachelor's Degree in in Mechanical Engineering or Technological orientation • &nbsp; &nbsp;Excellent command / proficiency of the English language. • &nbsp; &nbsp;Very good computer skills (MS Office). • &nbsp; &nbsp;Knowledge of Quality Assurance and Control Systems. • &nbsp; &nbsp;Good knowledge of mechanical drawing. • &nbsp; &nbsp;Familiarity with ERP systems (preferably SAP) is considered an asset. • &nbsp; &nbsp;Proactive and self-motivated, demonstrating initiative and adaptability. • &nbsp; &nbsp;Strong communication skills and teamwork oriented. • &nbsp; &nbsp;Results-driven, with a commitment to excellence. • &nbsp; &nbsp;Attention to detail, methodical, consistent, and a high sense of responsibility.&nbsp;The company offers:&nbsp; • &nbsp; &nbsp;Dynamic work environment • &nbsp; &nbsp;Career and Development Plan • &nbsp; &nbsp;Continuous Training • &nbsp; &nbsp;Competitive remuneration package • &nbsp; &nbsp;Additional insurance coverage

Θέσεις Εργασίας Ελεγκτής Ποιότητας Ελλάδα, Βιομηχανική Παραγωγή - Σελίδα 2

project technical engineer (2998)

Hellenic Cables

production engineer, medical devices

Rontis

quality analyst

DS Smith

gmp responsible

ALPLA Group

quality assurance administrator

FAMAR

senior r&d compliance officer

Elpen

packaging leader (σίνδος)

Ολυμπιακή Ζυθοποιία

product design and customer support engineer (3604)

Hellenic Cables

Jobily.gr

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