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Άλλο

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Εμπόριο Λιανικής

Ανθρώπινο Δυναμικό / HR

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&nbsp;We are searching to hire a&nbsp;Water Cycle Specialist to prepare tenders proposals, including technical and financial aspects, by developing technical solutions and communicating with relevant vendors/ third parties for technical analysis and equipment required. Also the role will manage third parties for technical input required and reviews the relevant analysis<h2>During your day you will:</h2><ul><li>Prepare the technical chapter of the tender submission by understanding project’s specifications, equipment and relevant risks, compiling the technical aspects of the proposal and collaborating with Thalis’ teams to develop a competitive bid</li><li>Manage Third Parties (Technical Consultants, Technology Providers, Subcontractors) and reviews and evaluates technical input produced by them, analyzes and validates calculations, technical specifications for Water Cycle processes</li><li>Formulate tender’s budget by taking into consideration project’s cost objects, profitability required etc. &nbsp;</li><li>Design Mechanical and Biological Processes and models for Water Cycle Management Projects (Hydraulic projects for water supply, irrigation, sewerage, water and wastewater treatment plants etc.)</li><li>Communicate with Third Parties (Vendors, Technical Consultants, Technology Providers, Subcontractors)</li><li>Stay abreast of emerging trends, technologies, equipment and regulations in the energy sector and specifically in the water cycle industry</li><li>Contribute to the preparation of appeals and questions for the open tenders</li><li>Evaluate and monitor of Water Cycle management projects during construction through site visits</li></ul><h2>What you need to stand out:</h2><ul><li>BSc degree in Mechanical/ Electrical/ Chemical Engineering</li><li>MSc degree in Engineering (relevant fields water cycle) will be considered an asset</li><li>Minimum 5 years previous experience in a similar role in water cycle management</li><li>Experience in engineering consulting offices will be considered an asset</li><li>Water cycle projects (water supply, sewerage, irrigation)</li><li>Water and waste water treatment projects</li><li>Process modeling and simulation for Water cycle, Mechanical projects</li><li>Excellent Knowledge on 2D and (3D Design non compulsory – preferably)</li><li>Very good command of the English language, written and verbal</li><li>Good knowledge in Microsoft Office Suite</li><li>Organizational and time management skills</li><li>Attention to detail</li></ul>&nbsp;&nbsp;Our Compass is the #ACTION#A_uthenticity#C_ompassion#T_eamwork#I_ntegrity#O_wnership#N_ever giving up&nbsp;&nbsp;What gives us energy:<ul><li>Friendly and fast paced environment, being always at the heart of the #action</li><li>Continuous learning to empower our teams</li><li>Career Development opportunities across the Motor Oil Group</li><li>Competitive compensation package</li></ul>&nbsp;&nbsp;*We @Motor Oil Group are an equal opportunity employer.Our hiring decisions are based solely on qualifications, merit, and business needs. We recruit, employ, train, and promote individuals without regard to race, color, religion, disability, sex, sexual orientation, gender identity, national origin, age, genetic characteristics, or any other protected status. Our commitment is to maintain an inclusive and diverse workforce where everyone has the opportunity to succeed.

Water Cycle Specialist

As a Safety Consultant, you will be responsible for understanding our customers’ Quality needs and business processes, providing expert guidance, discussing application changes, translating requirements into solution design, and configuring document and data management systems (e.g. Veeva Vault) for managing Drug Safety information across the organization.&nbsp;&nbsp;You will support a dedicated group of customers to help them transition on their digital transformation journey.&nbsp;&nbsp;&nbsp;&nbsp;Your key responsibilities&nbsp;<ul><li>Assist customers in implementing best practices within implementation / post-implementation programs aimed at ensuring their overall success.&nbsp;&nbsp;</li></ul><ul><li>Stay informed about best practices in the Pharmacovigilance field and offer actionable recommendations.&nbsp;&nbsp;</li></ul><ul><li>Technical abilities with willingness to “roll up your sleeves” to design solutions and configure the changes that meet customer needs.&nbsp;&nbsp;</li></ul><ul><li>Ability to collaborate and communicate with diverse stakeholders, including customer business and IT staff, to understand their requirements.&nbsp;</li></ul><ul><li>Establish trusted relationships with customer stakeholders.&nbsp;</li></ul><ul><li>Assist in the development and dissemination of thought leadership materials.&nbsp;</li></ul>&nbsp;Skills and attributes for success&nbsp;<ul><li>Bachelor’s or Master’s degree in Management Information Systems, Computer Science, Life Sciences, or related fields.&nbsp;</li></ul><ul><li>3+ years of consulting experience in configuring, supporting, or implementing software solutions.&nbsp;</li></ul><ul><li>Proven experience in a customer-facing role, managing expectations, facilitating difficult conversations, and delivering presentations or demos.&nbsp;</li></ul><ul><li>Strong background in Life Sciences with a particular interest in the Drug Safety domain.&nbsp;</li></ul><ul><li>Solid understanding of technologies used in Pharmacovigilance, particularly Veeva Vault applications (e.g. SafetyDocs, Safety, Workbench, Signal), and how PV consulting services can leverage and support these technologies.&nbsp;</li></ul><ul><li>Excellent verbal and written communication skills in English.&nbsp;&nbsp;</li></ul><ul><li>Ability to travel as required by the business.&nbsp;&nbsp;</li></ul>&nbsp;Ideally, you’ll also have&nbsp;<ul><li>Direct experience with Argus and/or other drug safety applications.&nbsp;</li></ul><ul><li>Knowledge of computer systems validation requirements (following a GxP system development lifecycle).&nbsp;</li></ul><ul><li>Good grasp of the business capabilities and drivers behind digital technology in health and life sciences, as well as the market forces and trends influencing industry changes.&nbsp;</li></ul><ul><li>Proficiency in additional European languages.&nbsp;</li></ul>&nbsp;What we look for&nbsp;&nbsp;We seek motivated, trustworthy professionals with strong communication skills and an analytical mindset. You thrive in high-performing teams, embrace challenges, and question the status quo. Curiosity, adaptability, and confidence to share ideas are essential. If you combine technical expertise with creativity, attention to detail, and a commitment to delivering exceptional quality while mentoring and collaborating, you’ll excel in our dynamic, multinational environment.&nbsp;&nbsp;

Senior Consultant - Safety - Life Sciences

As a Clinical&nbsp;Consultant, you will be responsible for understanding our customers’ Clinical&nbsp;needs and business processes, providing expert guidance, discussing application changes, translating requirements into solution design, and configuring document and data management systems (e.g. Veeva Vault) for managing Clinical&nbsp;information across the organization.&nbsp;&nbsp;You will support a dedicated group of customers to help them transition on their digital transformation journey.&nbsp;&nbsp;&nbsp;&nbsp;Your key responsibilities&nbsp;<ul><li>Assist customers in implementing best practices within implementation / post-implementation programs aimed at ensuring their overall success.&nbsp;&nbsp;</li></ul>&nbsp;<ul><li>Stay informed about best practices in the Clinical&nbsp;field and offer actionable recommendations.&nbsp;&nbsp;</li></ul>&nbsp;<ul><li>Technical abilities with willingness to “roll up your sleeves” to design solutions and configure the changes that meet customer needs.&nbsp;&nbsp;</li></ul>&nbsp;<ul><li>Ability to collaborate and communicate with diverse stakeholders, including customer business and IT staff, to understand their requirements.&nbsp;</li></ul>&nbsp;<ul><li>Establish trusted relationships with customer stakeholders.&nbsp;</li></ul>&nbsp;<ul><li>Assist in the development and dissemination of thought leadership materials.&nbsp;</li></ul>&nbsp;Skills and attributes for success&nbsp;<ul><li>Bachelor’s or Master’s degree in Management Information Systems, Computer Science, Life Sciences, or related fields.&nbsp;</li></ul>&nbsp;<ul><li>3+ years of consulting experience&nbsp;in configuring, supporting, or implementing software solutions.&nbsp;</li></ul>&nbsp;<ul><li>Proven experience in a customer-facing role, managing expectations, facilitating difficult conversations, and delivering presentations or demos.&nbsp;</li></ul>&nbsp;<ul><li>Strong background in Life Sciences with a particular interest in the Clinical&nbsp;domain (trial sponsors or contract research organizations (CROs)).&nbsp;</li></ul>&nbsp;<ul><li>Solid understanding of technologies used in Clinical, particularly Veeva Vault applications&nbsp;(e.g. eTMF, CTMS, SSU, Payments), and how Clinical&nbsp;consulting services can leverage and support these technologies.&nbsp;</li></ul>&nbsp;<ul><li>Excellent verbal and written communication skills in English.&nbsp;&nbsp;</li></ul>&nbsp;<ul><li>Ability to travel as required by the business.&nbsp;&nbsp;</li></ul>&nbsp;Ideally, you’ll also have&nbsp;<ul><li>Direct experience with Oracle Siebel, goBalto, BioClinica CTMS, Medidata Rave CTMS/Strategic Monitoring, Parexel IMPACT, Bio-Optronics Clinical Conductor, PhlexEView, Trial Interactive, DrugDev Site Selection and Payments, WingSpan eTMF, SiteZONE, Complion, Florence eBinders, Forte Oncore, eReg, NextDocs, Documentum, SharePoint, or other technologies utilized in managing clinical studies.&nbsp;</li></ul>&nbsp;<ul><li>Knowledge of computer systems validation requirements (following a GxP system development lifecycle).&nbsp;</li></ul>&nbsp;<ul><li>Good grasp of the business capabilities and drivers behind digital technology in health and life sciences, as well as the market forces and trends influencing industry changes.&nbsp;</li></ul>&nbsp;<ul><li>Proficiency in additional European languages.&nbsp;</li></ul>&nbsp;&nbsp;&nbsp;

Senior Consultant - Clinical - Life Sciences

JOB SUMMARY<ul><li>A highly productive, independent statistical data sciences lead ensuring excellence in the delivery of analysis ready datasets, analysis results, and displays such as tables, listings, and figures to advance research, development, and commercialization of the Pfizer portfolio following Pfizer SOPs and processes.</li><li>Ensures adherence to high quality statistical data sciences principles, processes and techniques in the production of clinical reports.</li><li>This role is the statistical data sciences point of contact at the study level, and will support at the asset/submission level.</li></ul>JOB RESPONSIBILITIES<ul><li>Will deliver through combination of oversight of in-house statistical data scientists / vendors / offshore support as well as through hands on application of statistical data sciences techniques (e.g., use of tools such as SAS, R, and Python to process clinical trial data and big data sources such as Real World Evidence to inform decision making).</li><li>Works with department leadership and project teams to establish strategy, timelines, and resourcing of deliverables for their study(ies).</li><li>Accountable for the quality and timely delivery of datasets, analysis results and displays required for their clinical study reports as well as other asset level deliverables they may contribute to under the leadership of the asset lead.</li><li>Ensures appropriate documentation across the lifespan of the study for deliverables and verifies proper Trial Master File filings when appropriate.</li><li>Ensures planning is in place for all deliverables including consideration of special data types and downstream uses of data.</li><li>Works with statisticians, statistical data science resources and other colleagues as appropriate to ensure clear specifications for deliverables are in place.</li><li>Will be knowledgeable in core safety standards as well as Therapeutic Area standards or Industry data standards for unique data types pertinent to their project. May aid in development of standards necessary for their study or asset.</li><li>Will contribute to department level initiatives.</li><li>Proactive at communicating potential issues to upper management.</li><li>Anticipates and solves routine problems, while developing the ability to solve complex problems using skills based on experience and extrapolation to new situations.</li><li>Supervises and supports a team, fostering collaboration and continuous improvement.</li></ul>QUALIFICATIONS / SKILLS<ul><li>Bachelor’s or Master’s (preferred) Degree in Statistics, Data Sciences, Biological Sciences, IT, or related field.</li><li>At least 5 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.</li><li>Clinical trials expertise with a thorough understanding of data operations required for the reporting of clinical trial data.</li><li>Good understanding of ICH and Regulatory Guidelines including submission requirements and data conformance (e.g., Pinnacle21).</li><li>Statistical Programming and SAS, R, or Python hands-on experience.</li><li>Familiarity with R packages, Shiny Apps, Markdown reports and other associated data science and data analytics tools and AI/ML highly desired.</li><li>Experience with Real World Evidence and other big data sources and associated standards (e.g.OMOP, JSON, ODHSI ) in support of regulatory filings desired.</li><li>Active participation in relevant industry groups (e.g., PHUSE, CDISC, IHD).</li><li>Routine problem solving skills, developing the ability to solve complex problems using skills based on experience and extrapolation to new situations.</li><li>Thorough understanding of clinical data and relevant data standards (e.g., CDISC).</li><li>Extensive knowledge of routine statistical methodology and its application to statistical data sciences.</li><li>Knowledge of vendor processes.</li><li>Demonstrated experience in developing successful partnerships within study teams.</li><li>Strong written and oral communication skills, and project management skills.</li><li>Ability to present technical information to a non-technical audience.</li><li>Proven ability to operate independently.</li><li>Some exposure working across international boundaries and cultures.</li><li>Ability to manage customer expectations.</li><li>Ability to manage work of others in a remote and/or global setting.</li></ul>

Manager, Statistical Data Sciences Lead Thessaloniki

As a RIM&nbsp;Consultant, you will be responsible for understanding our customers’ Regulatory&nbsp;needs and business processes, providing expert guidance, discussing application changes, translating requirements into solution design, and configuring document and data management systems (e.g. Veeva Vault) for managing Regulatory&nbsp;information across the organization.&nbsp;&nbsp;You will support a dedicated group of customers to help them transition on their digital transformation journey.&nbsp;&nbsp;&nbsp;&nbsp;Your key responsibilities&nbsp;<ul><li>Assist customers in implementing best practices within implementation / post-implementation programs aimed at ensuring their overall success.&nbsp;&nbsp;</li></ul>&nbsp;<ul><li>Stay informed about best practices in the Regulatory&nbsp;field and offer actionable recommendations.&nbsp;&nbsp;</li></ul>&nbsp;<ul><li>Technical abilities with willingness to “roll up your sleeves” to design solutions and configure the changes that meet customer needs.&nbsp;&nbsp;</li></ul>&nbsp;<ul><li>Ability to collaborate and communicate with diverse stakeholders, including customer business and IT staff, to understand their requirements.&nbsp;</li></ul>&nbsp;<ul><li>Establish trusted relationships with customer stakeholders.&nbsp;</li></ul>&nbsp;<ul><li>Assist in the development and dissemination of thought leadership materials.&nbsp;</li></ul>&nbsp;Skills and attributes for success&nbsp;<ul><li>Bachelor’s or Master’s degree in Management Information Systems, Computer Science, Life Sciences, or related fields.&nbsp;</li></ul>&nbsp;<ul><li>3+ years of consulting experience&nbsp;in configuring, supporting, or implementing software solutions.&nbsp;</li></ul>&nbsp;<ul><li>Proven experience in a customer-facing role, managing expectations, facilitating difficult conversations, and delivering presentations or demos.&nbsp;</li></ul>&nbsp;<ul><li>Strong background in Life Sciences with a particular interest in the Regulatory&nbsp;domain.&nbsp;</li></ul>&nbsp;<ul><li>Solid understanding of technologies used in Regulatory, particularly Veeva Vault applications&nbsp;(e.g. Submissions, Registrations, Submissions Archive, Publishing), and how RIM&nbsp;consulting services can leverage and support these technologies.&nbsp;</li></ul>&nbsp;<ul><li>Excellent verbal and written communication skills in English.&nbsp;&nbsp;</li></ul>&nbsp;<ul><li>Ability to travel as required by the business.&nbsp;&nbsp;</li></ul>&nbsp;Ideally, you’ll also have&nbsp;<ul><li>Direct experience with Amplexor, NextDocs, Documentum, SharePoint&nbsp;and/or other RIM applications.&nbsp;</li></ul>&nbsp;<ul><li>Knowledge of computer systems validation requirements (following a GxP system development lifecycle).&nbsp;</li></ul>&nbsp;<ul><li>Good grasp of the business capabilities and drivers behind digital technology in health and life sciences, as well as the market forces and trends influencing industry changes.&nbsp;</li></ul>&nbsp;<ul><li>Proficiency in additional European languages.&nbsp;</li></ul>&nbsp;What we look for&nbsp;We seek motivated, trustworthy professionals with strong communication skills and an analytical mindset. You thrive in high-performing teams, embrace challenges, and question the status quo. Curiosity, adaptability, and confidence to share ideas are essential. If you combine technical expertise with creativity, attention to detail, and a commitment to delivering exceptional quality while mentoring and collaborating, you’ll excel in our dynamic, multinational environment.&nbsp;&nbsp;What we offer you&nbsp;Ability to Shape your Future with Confidence by:&nbsp;<ul><li>Developing your professional growth:&nbsp;</li></ul><ul><li>You'll have unlimited access to educational platforms, EY Badges and EY Degrees, alongside support for certifications. You will experience personalized coaching and feedback, and gain exposure to international projects, through our expansive global network, empowering you to define and achieve your own success.&nbsp;</li></ul><ul><li>Dive into our innovative GenAI ecosystem, designed to enhance your EY journey and support your career growth. These advanced AI tools will empower you to focus on higher-value work and meaningful interactions, enriching your professional experience like never before.&nbsp;</li></ul><ul><li>Empowering your personal fulfilment: We focus on your financial, social, mental and physical wellbeing.&nbsp;</li></ul><ul><li>Our competitive rewards package, depending on your experience, includes cutting- edge technological equipment, ticket restaurant vouchers, a private health and life insurance scheme, income protection and an exclusive EY benefits club card that provides a wide range of discounts, offers and promotions.&nbsp;</li></ul><ul><li>Our flexible working arrangement (hybrid model) is defined based on your own preferences and team’s needs, and we enjoy other initiatives such as summer short Fridays and an EY Day Off.&nbsp;</li></ul><ul><li>Our commitment to a sustainable way of operating, encourages volunteerism, promotes sustainable practices and offers opportunities for you to create a positive societal impact.&nbsp;</li></ul><ul><li>Our pride lies in working at EY as one of the most recognized employers in Greece through our multiple awards received over the last 3 years (Top Employer, Great Place to Work and Best Workplace in Professional Services &amp; Consulting).&nbsp;</li></ul><ul><li>Fueling an inclusive culture: We prioritize a diverse, equitable and inclusive environment, where you’ll be embraced for who you are and empowered to use your voice to help others find theirs.&nbsp;</li></ul>&nbsp;

Senior Consultant- RIM- Life Sciences

EY Aqurance, a proud member of EY’s global organization, brings deep expertise in Life Sciences consulting and long-standing experience in digital transformation, working in close collaboration with teams across countries.&nbsp;&nbsp;As part of our team, you will support Life Sciences clients in improving processes, following modern platforms, and driving business value through structured analysis and problem-solving. You will gain exposure to international work, advanced technology, and AI-enabled approaches that shape how the industry operates.&nbsp;The Life Sciences R&amp;D and Quality Consulting Services team focuses on biotechnology, pharmaceutical, medical device manufacturers, and the medical technology industry. You will be an integral part of this team helping customers align business objectives from strategy to execution. This involves working with life sciences customers to develop business processes, and design and implement systems to effectively manage these areas governed by regulatory bodies globally (FDA, EMA, etc.).&nbsp;&nbsp;Do you have consulting and Quality systems experience and a passion for helping customers optimize their quality processes?&nbsp;&nbsp;As a Quality Consultant, you will be responsible for understanding our customers’ Quality needs and business processes, providing expert guidance, discussing application changes, translating requirements into solution design, and configuring document and data management systems (e.g. Veeva Vault) for managing Quality information across the organization.&nbsp;&nbsp;You will support a dedicated group of customers to help them transition on their digital transformation journey.&nbsp;&nbsp;&nbsp;&nbsp;Your key responsibilities&nbsp;<ul><li>Assist customers in implementing best practices within implementation / post-implementation programs aimed at ensuring their overall success.&nbsp;&nbsp;</li></ul><ul><li>Stay informed about best practices in the Quality field and offer actionable recommendations.&nbsp;&nbsp;</li></ul><ul><li>Technical abilities with willingness to “roll up your sleeves” to design solutions and configure the changes that meet customer needs.&nbsp;&nbsp;</li></ul><ul><li>Ability to collaborate and communicate with diverse stakeholders, including customer business and IT staff, to understand their requirements.&nbsp;</li></ul><ul><li>Establish trusted relationships with customer stakeholders.&nbsp;</li></ul><ul><li>Assist in the development and dissemination of thought leadership materials.&nbsp;</li></ul>&nbsp;Skills and attributes for success&nbsp;<ul><li>Bachelor’s or Master’s degree in Management Information Systems, Computer Science, Life Sciences, or related fields.&nbsp;</li></ul><ul><li>3+ years of consulting experience in configuring, supporting, or implementing software solutions.&nbsp;</li></ul><ul><li>Proven experience in a customer-facing role, managing expectations, facilitating difficult conversations, and delivering presentations or demos.&nbsp;</li></ul><ul><li>Strong background in Life Sciences with a particular interest in the Quality domain.&nbsp;</li></ul><ul><li>Solid understanding of technologies used in Quality, particularly Veeva Vault applications (e.g. QualityDocs, QMS, Training, LIMs), and how Quality consulting services can leverage and support these technologies.&nbsp;</li></ul><ul><li>Excellent verbal and written communication skills in English.&nbsp;&nbsp;</li></ul><ul><li>Ability to travel as required by the business.&nbsp;&nbsp;</li></ul>&nbsp;Ideally, you’ll also have&nbsp;<ul><li>Direct experience with Track Wise and/or other quality applications.&nbsp;</li></ul><ul><li>Knowledge of computer systems validation requirements (following a GxP system development lifecycle).&nbsp;</li></ul><ul><li>Good grasp of the business capabilities and drivers behind digital technology in health and life sciences, as well as the market forces and trends influencing industry changes.&nbsp;</li></ul><ul><li>Proficiency in additional European languages.&nbsp;</li></ul>&nbsp;What we look for&nbsp;We seek motivated, trustworthy professionals with strong communication skills and an analytical mindset. You thrive in high-performing teams, embrace challenges, and question the status quo. Curiosity, adaptability, and confidence to share ideas are essential. If you combine technical expertise with creativity, attention to detail, and a commitment to delivering exceptional quality while mentoring and collaborating, you’ll excel in our dynamic, multinational environment.&nbsp;&nbsp;What we offer you&nbsp;Ability to Shape your Future with Confidence by:&nbsp;<ul><li>Developing your professional growth:&nbsp;</li></ul><ul><li>You'll have unlimited access to educational platforms, EY Badges and EY Degrees, alongside support for certifications. You will experience personalized coaching and feedback, and gain exposure to international projects, through our expansive global network, empowering you to define and achieve your own success.&nbsp;</li></ul><ul><li>Dive into our innovative GenAI ecosystem, designed to enhance your EY journey and support your career growth. These advanced AI tools will empower you to focus on higher-value work and meaningful interactions, enriching your professional experience like never before.&nbsp;</li></ul><ul><li>Empowering your personal fulfilment: We focus on your financial, social, mental and physical wellbeing.&nbsp;</li></ul><ul><li>Our competitive rewards package, depending on your experience, includes cutting- edge technological equipment, ticket restaurant vouchers, a private health and life insurance scheme, income protection and an exclusive EY benefits club card that provides a wide range of discounts, offers and promotions.&nbsp;</li></ul><ul><li>Our flexible working arrangement (hybrid model) is defined based on your own preferences and team’s needs, and we enjoy other initiatives such as summer short Fridays and an EY Day Off.&nbsp;</li></ul><ul><li>Our commitment to a sustainable way of operating, encourages volunteerism, promotes sustainable practices and offers opportunities for you to create a positive societal impact.&nbsp;</li></ul><ul><li>Our pride lies in working at EY as one of the most recognized employers in Greece through our multiple awards received over the last 3 years (Top Employer, Great Place to Work and Best Workplace in Professional Services &amp; Consulting).&nbsp;</li></ul><ul><li>Fueling an inclusive culture: We prioritize a diverse, equitable and inclusive environment, where you’ll be embraced for who you are and empowered to use your voice to help others find theirs.&nbsp;</li></ul>&nbsp;

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