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Supports Compliance with Nestlé Quality Management System requirements in the unit, as well as Food Safety &amp; Quality requirements in Supply Chain (Storage &amp; Distribution, Inter-Market Supply and Vendor Management). &nbsp;A day in the life…&nbsp;<ul><li>Coordinate validation of quality inspection practices and equipment status according to standards.</li><li>Verify the quality standards at the shopfloor.</li><li>Execute process inspection release and status control according to authorization.</li><li>Use recorded data to perform analysis and prepare reports.</li><li>Demonstrate active compliance with hygiene, safety and quality requirements based on factory procedures.</li><li>Execute quality inspections according to Quality Management System for raw/pack and non-supply chain materials. &nbsp;</li></ul>What makes you successful&nbsp;<ul><li>University Degree in Food Technology (AEI or TEI) or Chemistry&nbsp;</li><li>1-2 years of previous experience in quality control department would be a plus</li><li>Advanced knowledge of MS Office</li><li>Result focus, initiative, proactive cooperation</li><li>Intelligent, ambitious, responsible, efficient and with team spirit</li><li>Fluency in Greek &amp; English</li><li>Knowledge of ISO &amp; HACCP processes would be an advantage</li><li>Experience in projects is desirable &nbsp;</li></ul>Why you should apply&nbsp;Enjoy the wide range of Nestlé benefits such as:&nbsp;<ul><li>competitive salary &amp; performance bonus&nbsp;</li><li>meal vouchers&nbsp;</li><li>comprehensive Pension, Health Care &amp; Life Insurance programs&nbsp;</li><li>increased Parental leaves for both caregivers and Baby Support plan&nbsp;</li><li>Flexible Work policy&nbsp;</li><li>Wellbeing and Recognition days off&nbsp;</li><li>“Bring Your Pet At Work” &amp; Pet Support plan&nbsp;</li><li>free car parking&nbsp;</li><li>in-house restaurant and mini market&nbsp;</li><li>participation to health and wellness activities and much more&nbsp;</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.&nbsp;

Quality Assurance Analyst, 12month contract

We are looking for a highly motivated graduate to join our dynamic team and contribute to initiatives in Manufacturing. You will work alongside Senior Managers of the Factory, taking on tasks in the area of Manufacturing while leveraging digital tools and technologies to drive efficiency and innovation. Adaptability, prioritization, organization, and time management remain critical, combined with a strong interest in digital transformation. &nbsp;&nbsp; A day in the life<ul><li>Lead continuous improvement activities by identifying opportunities and ensuring effectiveness.</li><li>Lead data analysis, digitalization initiatives, and process optimization projects.</li><li>Generate and issue instructions to factory shop floor and facilitate execution.</li><li>Participate in Daily Operational Reviews and Production Reviews.</li></ul> &nbsp;What makes you successful&nbsp;<ul><li>University Degree in Engineering or Food Technology.</li><li>1-2 years of working experience in a technical field, preferably food manufacturing or consumer goods industry.</li><li>Fluency in Greek &amp; English.</li><li>Strong digital mindset and ability to work with digital tools for manufacturing optimization.</li><li>Experience with Business Analytics (i.e. MS Power Platform) is considered a significant plus.&nbsp;</li><li>Computer literacy – including PowerBI, MS-Office.</li><li>SAP knowledge would be a plus.</li><li>Driving License is required.</li></ul>&nbsp;Why you should apply&nbsp; Enjoy the wide range of Nestlé benefits such as:&nbsp;<ul><li>competitive salary &amp; performance bonus</li><li>meal vouchers&nbsp;</li><li>comprehensive Pension, Health Care &amp; Life Insurance programs&nbsp;</li><li>increased Parental leaves for both caregivers and Baby Support plan&nbsp;</li><li>Flexible Work policy&nbsp;</li><li>Wellbeing and Recognition days off&nbsp;</li><li>“Bring Your Pet At Work” &amp; Pet Support plan&nbsp;</li><li>free car parking&nbsp;</li><li>in-house restaurant and mini market&nbsp;</li><li>participation to health and wellness activities and much more&nbsp;</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&nbsp; Take full advantage of unlimited development opportunities through an extensive physical, virtual and hybrid learning ecosystem, both at local and international level&nbsp;

Project Trainee, 12month contract

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

HELLENIC CABLELS S.A.&nbsp;is seeking a Laboratory (High Voltage) Engineer to join our team at our state-of-the-art facility in Corinth that focuses on the production of high and extra high voltage submarine cables&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Duties and Responsibilities&nbsp;<ul><li>Supervise, coordinate and perform electrical / High Voltage tests &amp; measurements</li><li>Issue and review technical documents</li><li>Study international specifications and standards and participate in technical meetings</li><li>Issue operating &amp; safety instructions</li><li>Train and develop laboratory personnel</li><li>Resolve emerging problems/deficiencies and address open technical issues</li><li>Process and interpret measured data</li><li>Plan, prioritize &amp; oversee the laboratory operating schedule to ensure maximum performance and minimum delay</li><li>Specify and monitor Lab KPI’s</li><li>Ensure the safe use and regular maintenance of the Laboratory equipment</li><li>Foresee and suggest future needs in equipment/ special constructions</li></ul>&nbsp;Qualifications and Experience&nbsp;<ul><li>Diploma in Electrical Engineering (5-year integrated program - preferably Energy sector)&nbsp;</li><li>Excellent knowledge of MS Office and MS Project</li><li>Fluent in English</li><li>Strong analytical skills to evaluate problems/opportunities and drive cost- effective solutions</li><li>Effective interpersonal, communication and teamwork skills</li><li>Strong organization skills to prioritize workload</li><li>Good numerical skills and an understanding of statistics</li><li>Familiar with Quality Assurance Regulations</li><li>Time-management skills</li></ul>&nbsp;The Company Offers&nbsp;<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>&nbsp;

LABORATORY ENGINEER (3642)

As an Assembly-Packaging Machine Operator Expert&nbsp;you will be responsible for the operation and monitoring of Assembly &amp; Packaging machines. You will ensure the safe and efficient operation of these machines by carrying out the 1st level of maintenance, which includes cleaning, lubrication, product set ups and adjustments. You will inform your supervisor of the machine efficiency, as well as, for any corrective and/or improvement actions that need to be taken. You will also participate in the preventive maintenance of these machines. You will be responsible for the training of the new machine operators. Finally, you will follow HSE and Quality regulations, as these are defined in our internal procedures.&nbsp;Main Responsibilities/Tasks:•&nbsp;&nbsp; &nbsp;Start up and operation of Assembly &amp; Packaging machines •&nbsp;&nbsp; &nbsp;Responsible for 1st level of maintenance •&nbsp;&nbsp; &nbsp;Accountable for training new machine operators•&nbsp;&nbsp; &nbsp;Participate in machine improvements•&nbsp;&nbsp; &nbsp;Participate in preventive maintenance •&nbsp;&nbsp; &nbsp;Monitor and record machine interventions •&nbsp;&nbsp; &nbsp;Monitor and record product and machine parameters •&nbsp;&nbsp; &nbsp;Carry out product changeovers and machine set ups •&nbsp;&nbsp; &nbsp;Required to inform the Shift Supervisor and Production Supervisor •&nbsp;&nbsp; &nbsp;Communicate with QA, QC, Industrialization, Central Maintenance •&nbsp;&nbsp; &nbsp;Able to identify safety issues and handle reporting to the Shift Supervisor •&nbsp;&nbsp; &nbsp;Responsible for Quality Control of final product •&nbsp;&nbsp; &nbsp;Perform pre-determined audit controls according to the inspection plan •&nbsp;&nbsp; &nbsp;Το comply with health, safety and environmental rules in accordance with company's policy and prescribed procedures &nbsp;Qualifications&nbsp;Required Skills• Technical School or Technical Institute Degree in Mechanical or Electrical Engineering, will beconsidered as a prerequisite• Certified with minimum licence of Technician (Mechanical or Electrical)• Adequate knowledge of English language (both written and verbal)• Advanced PC literacy (especially MS Office)• Work in shifts&nbsp;Preferred Skills• 3 years of working experience, preferably in industrial field&nbsp;Other Skills•Strong interpersonal skills to collaboratively work with BIC Team Members•Strong attention to detail, work ethic, sense of urgency, and desire to deliver results.

ASSEMBLY-PACKAGING MACHINE OPERATOR EXPERT

<ul><li>Επίβλεψη και εκτέλεση παραγωγής, χειρισμός και επίβλεψη ορθής λειτουργίας μηχανών ενσάκισης, ενσάκισης (big bag) και παλετοποίησης</li><li>Σωστή και ασφαλή λειτουργία του τομέα</li><li>Τήρηση των κανόνων ορθής παραγωγής και του ελέγχου της ποιότητας</li><li>Αναζήτηση νέων ευκαιριών βελτίωσης της απόδοσης του τμήματος, και πρόταση καινοτόμων μεθόδων ή αγορών (προμήθειες) και τρόπους συντήρησης που θα επιφέρουν αποτελεσματικότητα και οικονομία στην επιχείρηση.</li></ul>Απαραίτητα Προσόντα<ul><li>Πτυχίο κλάδων Μηχανολογίας / Ηλεκτρολογίας / Αυτοματισμών (η οποιασδήποτε άλλης τεχνικής ιδιότητας )</li><li>Κατ΄ ελάχιστον 3έτης εργασιακή εμπειρία σε τομέα βιομηχανίας ,παραγωγής ή συντήρησης</li><li>Άριστη γνώση χρήσης Η/Υ (MS Office , internet, εμπειρία βιομηχανικού λογισμικού)</li><li>Άριστη ικανότητα οργάνωσης χρόνου και ικανότητα επίτευξης στόχων</li><li>Δυνατότητες εργασίας σε βάρδιες</li></ul>Παροχές<ul><li>Άριστο εργασιακό περιβάλλον</li><li>Ανταγωνιστικό πακέτο αποδοχών/ πλήρης απασχόλησης</li><li>Συνεχή εκπαίδευση</li><li>Ιδιωτική Ασφάλιση Υγείας</li><li>Προοπτικές επαγγελματικής εξέλιξης</li></ul>

Υπεύθυνος Βάρδιας Παραγωγής Λιπασμάτων

Lead the company’s environmental performance strategy, ensure full regulatory compliance, and drive programs that minimize environmental impacts (climate, air &amp; water emissions, biodiversity, resources/waste), with transparent reporting to Management and stakeholders. The role also has overall responsibility for the operation and oversight of the physico‑chemical Industrial Wastewater Treatment Plant.&nbsp;Responsibilities<ul><li>Responsible for the communication and implementation of company’s environmental policy and Management’s commitment on environmental issues as well as for the training of the Company's personnel in this specific field.</li><li>Ensure end‑to‑end compliance with environmental permits and applicable legislation; coordinate the implementation of recommendations from competent public authorities.</li><li>Establish internal regulations and procedures and implement a comprehensive waste management program, in close collaboration with department heads and engineers.</li><li>Set up, monitor, and evaluate environmental KPIs and monitoring programs; drive corrective and preventive actions and report results to Management and authorities.</li><li>Prepare and submit required environmental studies/permits and reports (e.g., Environmental Impact Assessment, GHG emissions permit, Waste Management Plan, E‑PRTR reporting).</li><li>Develop the Environmental Management System (EMS) and ensure its effective operation and certification.</li><li>Act as liaison with regulatory/inspection authorities (e.g., Ministry of Environment &amp; Energy, Region of Central Greece); accompany inspectors onsite and recommend procedural changes as needed.</li><li>Oversee the Wastewater Treatment Plant operation, ensuring compliance and approved discharge limits; organize sampling/analyses (pH, conductivity, BOD/COD, heavy metals) and maintain complete records (e.g., ΗΜΑ) for authorities and management.</li><li>Coordinate preventive maintenance and reliability of critical assets (balancing tanks, aeration/settling/filtration/RO systems), contingency plans, and handling of emergency wastewater (e.g., firefighting water).</li><li>Develop and manage the Environmental budget and oversee environmental suppliers/partners.</li></ul>&nbsp;Qualifications<ul><li>Degree in Environmental Engineering or Chemical Engineering or Mechanical Engineering from a Polytechnic School</li><li>Postgraduate studies and specialization desirable</li><li>Work experience for at least 5 years in a similar position with compliance / system responsibility</li><li>Excellent knowledge of Environmental issues</li><li>Strong leadership, influencing, negotiation, change management, communication skills</li></ul>• Excellent knowledge of English• Knowledge of information systems&nbsp;Skills<ul><li>Excellent problem-solving skills and attention to detail.</li><li>Strong communication and leadership abilities to work cross-functionally.</li><li>Ability to manage multiple projects and prioritise&nbsp;tasks effectively.</li></ul>&nbsp;BenefitsCompetitive remuneration package and a wide range of benefits

ENVIRONMENTAL MANAGER (3679)

Position Purpose<ul><li>Performs proactive safety surveillance and risk management to effect product safety signal detection &amp; evaluation, risk assessment and safety risk minimization</li><li>Works with other Pfizer functions engaged in benefit-risk management (Regulatory Affairs, Quality, CMO, Corporate Audit, etc) to enable one medical voice</li><li>Articulates clear and informed medical judgement to enable sound business decisions and to enable productive engagement with health authorities.</li></ul>Primary Responsibilities<ul><li>Act as a point of contact for Safety in the Asset Teams, ensuring a unified communication on safety matters and representing WWS position(s) on safety</li><li>Chairs RMCs and Core Working Groups for his/her assigned products with oversight</li><li>Represents Pfizer WWS at internal (e.g. governance and business unit disease area leadership teams) and external forums&nbsp; (e.g. regulatory authority and business partner interactions) as agreed with Manager</li><li>Evaluates safety data of any source with oversight, identifies and analyzes safety signals, and presents medical evaluation of safety signals and benefit-risk assessments to the appropriate forums</li><li>Provides disease area specific pharmacovigilance expertise, and applies this to various business unit products assigned to him/her</li><li>Assists with preparation of basic action plans to address risk and benefit-risk issues, often requiring cross-functional activity to address safety issues and risk minimization plans</li><li>Prepares and contributes to written safety assessments and benefit-risk evaluations</li><li>Reviews and approves, as appropriate, safety documents including those pertaining to the B-R profile of Pfizer’s products</li><li>Ensures consistency of safety risk messaging for a particular product or class of products, across multiple indications/BUs. Represents SSRM on due diligence activities</li><li>Identifies opportunities for consistency and standards for safety surveillance and risk management processes</li><li>Innovates, champions and implements novel approaches to safety surveillance and risk management across Pfizer’s portfolio of products: engages in continuous improvement initiatives, Safety Sciences Research &amp; Communications activities, including methodological improvements</li><li>Engages in inspection readiness support including provision of data to project managers for metrics and activity tracking</li><li>Develops a culture of courage, excellence, equity and joy within the team including regular communications, coaching, and mentoring of the team as required.</li></ul>Technical Skill Requirements<ul><li>Medical Degree or equivalent.</li><li>Oncology background preferred not required.</li><li>Understanding of aggregate safety data and signal assessment methodology, and ability to perform benefit-risk assessments</li><li>Ability to perform safety data review, safety data assessment, Clinical safety signal identification, risk identification and risk management</li><li>Understanding of the scientific basis for therapies and drug-induced diseases</li><li>Ability to lead a cross functional team and lead through example, commitment and enthusiasm in a matrixed environment with minimal oversight</li><li>Strong scientific and medical knowledge, including fluency in the medical literature</li><li>Ability to integrate data to support benefit/risk decision-making</li><li>Understanding of statistics and analytical tools</li><li>Knowledge of global safety/regulatory issues and concerns as they relate to the business or clinical research-based compound development</li><li>Effective verbal and written communication skills.</li></ul>&nbsp;&nbsp;

Job Ads Intern Greece, Industrial Production - Page 2

quality assurance analyst, 12month contract

Nestlé

project trainee, 12month contract

Nestlé

production engineer, medical devices

Rontis

quality analyst

DS Smith

laboratory engineer (3642)

ElvalHalcor

assembly-packaging machine operator expert

BIC

υπεύθυνος βάρδιας παραγωγής λιπασμάτων

Agrohellas Α.Ε.

υπεύθυνος βάρδιας παραγωγής λιπασμάτων

Agrohellas Α.Ε.

environmental manager (3679)

ElvalHalcor

safety risk lead, sr. manager 4937297

Pfizer Hellas

Jobily.gr

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