Überblick über die Statistik des Gehaltsniveaus für "Safety Manager in Deutschland"

Location: Spain - Home based          Schedule: Freelance, Various FTEs                                      CROMSOURCE is a growing international CRO dedicated to a quality-focused approach with a collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Freelance Clinical Project Manager II, to join their clinical operations team in Spain. This is a full-time opportunity. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                          As a Clinical Project Manager II, you will be responsible for managing the clinical projects and ensuring the quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines, and other applicable regulations.                                    Join our team and help us deliver clinical trials that will improve patients' lives.            Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projectsManage all project-specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team membersKeep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assignedKnowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areasAssure the proper timelines of the assigned projectsManage the budget for the projectMonitor the workload and the performance of the project teamPlan and monitor the tasks of the team in the specific areasCoordinate the Clinical Research Associates and Clinical Monitors activityCollaborate with Clinical Trial Administrators and Clinical Research Associates in terms of local authorities' approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activitiesAssist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDeliver project-specific trainingOrganise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetingsProvide project updates to the Sponsor, Senior Project Manager, and Project Director/Leader as requiredInform the Project Director/Leader about any issuesPerform co-monitoring visits for the assigned clinical projects as necessaryAct as a tutor for Project Coordinators and Project Managers IMaintain relationships with the Sponsor, including providing project updatesPrepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying with enforcing Company procedures Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similarExcellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel The Application Process     Once you have submitted your CV, you will receive an acknowledgment email. If you have the requirements we need, you will be invited for a phone interview as the first step.            If you would like to discuss the role before applying through the website @ http://www.cromsource.com/careers/job-vacancies please contact [email protected] for more information.          Who will you be working for?          About CROMSOURCE        CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                          Our Company Ethos     Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. Continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates.          CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.          Keywords: Senior Project Manager, Clinical Project Manager, Senior Study Manager, Study Management Associate, Project Management Associate, Clinical, Drugs, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, CRO, Clinical Research Organisation, Contract Research Organisation  Skills: Clinical Project Manager, Clinical Study Manager, clinical trials, ICH-GCP, Project Management, EnglishLocation: SpainShare: LinkedIn Facebook Twitter Email

Location: Poland - Home based        Schedule: Freelance, Various FTEs                                    CROMSOURCE is a growing international CRO dedicated to a quality-focused approach with a collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Freelance Clinical Project Manager I, to join their clinical operations team in Poland. This is a full-time opportunity. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                      As a Project Manager, you will be responsible, for oversight of assigned clinical projects ensuring the quality of services in accordance with contractual obligations, applicable SOPs, ICH/GCP guidelines, and other, applicable regulations. You may also act as Project Director/Leader, depending on the complexity of the projects.   Join our team and help us deliver clinical trials that will improve patients' lives.                   Main Tasks and Responsibilities:Manages the development and planning of clinical projects, interacting with the Sponsor and the Investigators and coordinating the project team memberOversees the application process for clinical studies, in force in the country(ies) of work. Verifies the assigned project activities plan and timelines and the related critical stateManages the budget of the projectParticipates in Monitor's and Investigator's MeetingsProvides project updates to the Sponsor and to the Project Director/Leader and to the Clinical Department Director; participates in update meetings.Informs Project Director/Leader and the Clinical Department Director about any issues that can jeopardize the business relationship with the SponsorSupervises the team in relation to monitoring including submissions, site visits, ensuring compliance with ICH/GCP guidelines and applicable laws and regulationsUndertakes workload and performance assessments of the project team working with the Clinical Research Department Director to ensure adequate support levelsMay provide oversight and mentoring for junior staff assigned to the projects.Supervises the archiving activitiesSupervises, in the overall management of the project, the assigned Biometrics team and all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc…)Assists the Medical Monitor (MEM) in preparing protocols, Case Report Forms (CRFs), and final Clinical Study Reports (CSRs)Performs, if necessary, co-monitoring visits for the assigned clinical projectsMay act as Feasibility Associate (FEA) after appropriate and documented trainingMay prepare SOPs relating to clinical research activities in collaboration with the Quality System Unit (QSU)Arranges and collaborate with the assigned Clinical Research Department Director, in identifying the project-specific training of the project team and in delivering them Education and Experience:University Degree in scientific, medical, or paramedical disciplinesUp to three 3 years of project management experience in the CRO/Pharmaceutical industryStrong knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel The Application Process   Once you have submitted your CV, you will receive an acknowledgment email. If you have the requirements we need, you will be invited for a phone interview as the first step.        If you would like to discuss the role before applying through the website @ http://www.cromsource.com/careers/job-vacancies please contact [email protected] for more information.      Who will you be working for?      About CROMSOURCE      CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                      Our Company Ethos   Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. Continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates.      CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.      Keywords: Senior Project Manager, Clinical Project Manager, Senior Study Manager, Study Management Associate, Project Management Associate, Clinical, Drugs, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, CRO, Clinical Research Organisation, Contract Research Organisation  Skills: Clinical Project Manager, Clinical Study Manager, clinical trials, ICH-GCP, Project Management, EnglishLocation: PolandShare: LinkedIn Facebook Twitter Email

Job Description Har du erfarenhet av ledarskap inom arbetsmiljö? Just nu letar vi på Northvolt ETT i Skellefteå med ljus och lykta efter en chef till vårt team! Genom att arbeta hos oss får du möjligheten att vara med i byggandet av en av Europas första storskaliga batterifabriker, samt elektrifieringen och övergången till ett samhälle fritt från koldioxidutsläpp. Som chef för vår Hälsa-och Säkerhetsavdelning kommer du ansvara för att etablera våra processer och mål, samt utveckla en kultur kring och säkerhetsställa säkra arbetssätt i vår fabrik. Den här rollen kommer erbjuda dig att arbeta både operativt och strategiskt i vårt ledarskapsteam för Hälsa och Säkerhet. Du kommer att leda, coacha samt bygga ditt team, bestående av Hälsa- och säkerhetsingenjörer, där ni tillsammans kommer arbeta för att etablera vår arbetsmiljö på Northvolt ETT i Skellefteå.AnsvarsområdenLeda och coacha Hälsa- och SäkerhetsteametImplementera planer, rutiner och processer för Hälsa och Säkerhet för hela fabrikenUtveckla management systems för Hälsa och SäkerhetVara en del av och stötta operativt/dagligt arbeteLeda och stötta i att sätta upp och följa krav samt lagstiftningar från externa och interna behovLeda undersökningar/root cause analysis vid incidenter. Rapportera framgångar, problem och statistikCoacha och träna chefer och anställda för att stärka vår Hälsa-och Säkerhetskultur

Location: Italy - Home or office based      Schedule: Permanent, Full-time                 Do you want to join a team that is passionate about making a difference in drug and medical device development?  CROMSOURCE, a growing CRO, is recruiting for a Senior Clinical Project Manager to join their clinical operations team. This is a permanent opportunity in Italy. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                          As a Senior Clinical Project Manager, you will be responsible, for oversight of assigned clinical projects ensuring the quality of services in accordance with contractual obligations, applicable SOPs, ICH/GCP guidelines, and other, applicable regulations. You may also act as Project Director/Leader, depending on the complexity of the projects. Previous experience with respiratory and oncology trials is preferred. A minimum of 3 years of experience with a CRO is needed.           Join our team and help us deliver clinical trials that will improve patients' lives.                               Main Tasks and Responsibilities:Manages the development and planning of clinical projects, interacting with the Sponsor and the Investigators, and coordinating the project team members.Oversees the application process for clinical studies, in force in the country(ies) of work. Verifies the assigned project activities plan and timelines and the related critical state.Manages the budget of the project.Participates in Monitor's and Investigator's MeetingsProvides project updates to the Sponsor and to the Project Director/Leader and to the Clinical Department Director; participates in update meetings.Informs Project Director/Leader and the Clinical Department Director about any issues that can jeopardize the business relationship with the Sponsor.Supervises the team in relation to monitoring including submissions, site visits, ensuring compliance with ICH/GCP guidelines and applicable laws and regulations.Undertakes workload and performance assessments of the project team working with the Clinical Research Department Director to ensure adequate support levels.May provide oversight and mentoring for junior staff assigned to the projects.Supervises the archiving activities.Supervises, in the overall management of the project, the assigned Biometrics team and all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc…)Assists the Medical Monitor (MEM) in preparing protocols, Case Report Forms (CRFs), and final Clinical Study Reports (CSRs)Performs, if necessary, co-monitoring visits for the assigned clinical projects.May act as Feasibility Associate (FEA) after appropriate and documented training.May prepare SOPs relating to clinical research activities in collaboration with the Quality System Unit (QSU)Arranges and collaborate with the assigned Clinical Research Department Director, in identifying the project-specific training of the project team and in delivering them. Education and Experience Required:University Degree in scientific, medical, or paramedical disciplines with 3 years of experienceSignificant 3 years of experience in clinical project management in the CRO/pharmaceutical industryExcellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel. The Benefits of Working in Italy:· Meal vouchers· Mobile phone if requested by the Line Manager· Dedicated Line Manager Who will you be working for?                                    About CROMSOURCE                       CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                                                    Our Company Ethos                  Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they can develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built, and close management and training is the core instrument to develop and maintain highly qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below-industry average turnover rates.                                     The Application Process                  Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements we need, you will be invited for a phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.               If you would like to discuss the role before applying through the website @ http://www.cromsource.com/careers/job-vacancies please contact [email protected] for more information.                                        CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.                                     Keywords: Project Manager, Clinical Project Manager, CRO, Clinical Research Organisation, Contract Research Organisation, Clinical, Drugs, Medical Devices, Medical Device, Project Management, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, Respiratory, Oncology, OphthalmologySkills: Clinical Project Manager, Clinical Study Manager, Clinical Trial Manager, Senior Clinical Project Manager, clinical trials, CRO, Medical Devices, Study ManagementLocation: ItalyShare: LinkedIn Facebook Twitter Email

Location: Belgium - Home based    Schedule: Permanent, Full-time                           Do you want to join a team that is passionate about making a difference in drug and medical device development?  CROMSOURCE, a growing CRO, is recruiting for a Senior Clinical Project Manager to join their internal team in Belgium. This role is a full-time permanent opportunity. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                                  As a Senior Clinical Project Manager, you will be responsible for managing the clinical projects ensuring quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines and other applicable regulations.                             Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projects.Manage all project specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team members.Keep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assigned.Knowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areas.Assure the proper timelines of the assigned projects.Manage the budget for the project.Monitor the workload and the performance of the project team.Plan and monitor the tasks of the team in the specific areas.Coordinate the Clinical Research Associates and Clinical Monitors activity.Collaborate with he Clinical Trial Administrators and Clinical Research Associates in terms of local authorities approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activities.Assist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDeliver project specific trainings.Organise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetings.Provide project updates to the Sponsor, Senior Project Manager and Project Director/Leader as required.Inform the Project Director/Leader about any issues.Perform co-monitoring visits for the assigned clinical projects as necessary.Act as a tutor for Project Coordinators and Project Manager IMaintain relationships with the Sponsor, including providing project updates.Prepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying and enforcing Company procedures. Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similar.Excellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel The Benefits of Working in Belgium:Competitive SalaryGroup and hospitalisation insuranceElectronic meal vouchersInternet reimbursement The Application Process           Once you have submitted your CV, you will receive an acknowledgement email. If you have the requirements we need, you will be invited for phone interview as the first step.                        If you would like to discuss the role before applying through the website @ http://www.cromsource.com/careers/job-vacancies please send an mail to: [email protected] for more information.                     Who will you be working for?                                            About CROMSOURCE                           CROMSOURCE is a family owned international, full-service Contract Research Organisation who, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus on the heart of everything we do.                                                            Our Company Ethos                      Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built, and close management and training is the core instrument to develop and maintain highly qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology.   The success of these core values is evidenced by our below industry average turnover rates.                                                         CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.                                             Keywords: Senior Project Manager, Clinical Project Manager, Senior Study Manager, Study Management Associate, Project Management Associate, Clinical, Drugs, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, CRO, Clinical Research Organisation, Contract Research OrganisationSkills: Clinical Project Manager, Clinical Study Manager, Clinical Trial Manager, Senior Clinical Project Manager, clinical trials, CRO, Medical Devices, Study ManagementLocation: BelgiumShare: LinkedIn Facebook Twitter Email

Applied Materials is the world market leader for special systems and manufacturing processes in semiconductor, electronics and display technology. We not only provide the technology that powers nearly every new chip and advanced display in the world, but also our innovations shape the technology of the future. ~33,000 employees worldwide work in research and development, production, sales, and service.Our subsidiary, Integrated Circuit Testing GmbH (ICT GmbH), with ~160 employees, develops and produces electron microscopes, the heart of our machines, which monitor processes in semiconductorproduction and classify the smallest defects on wafers. To meet the rapidly increasing demand from our customers in the semiconductor industry, our location near Munich, Germany is constantly growing.The mission of the MFG Delivery Manager is to lead a team to deliver columns, or other services as defined in the scope, on time with world class quality, to meet our business demand, while developing proficient & motivated team and collaborating broadly across the organization. You will directly manage a large group of employees and will be responsible for their safety, well-being and personal growth. Also you will work closely to manage the day to day activities to meet our delivery performance goals. Additionally, you will collaborate with all the different functions in the organization, at GE and IL, to ensure proactively that the MFG in specific and the Operations when requested, will be ready to support any business demand, while driving for continuous improvement of our performance.Key Responsibilities:As a Manufacturing Manager, oversees full responsibility over a product, or services to deliver all our commitments to customer Define and control the objectives, drive for effective and efficient performance, continually improving, starting from NPI to SPI, at out facility near Munich and our customersManage Ops, SR and AOP creation, ongoing integration and direction ownership on cross - org activitiesBuild the team – motivation, proficiency, flexibility, personal development and career pathReview our future business demand, take active role in defining and executing the strategies and long-term plansLook for the shortfalls and opportunities; act proactively to resolve themEnsure our working environment is safe, organized, equipped with all necessary and healthyEnsures compliance with company policies including (but not limited to) production floor and labs, Intellectual property, confidentiality, ISO, safety and others as required. Establishes close collaboration with other departments, defines and enables clear handshakes and flawless executionSkills and Experience required: Strong leadership skills, experienced in leading teamsStrong analytical skills to be able to analyze situation, define causes and execute recovery plansGreat communication and presentation skillsProject management skills Ability to work independentlyHands on mentality, eager to learn and adoptCollaborative, ability to work and contribute to integrated teamsVery good English as well as German skills both written and verbalYou’re eager to:Be a part of highly qualified engineering team, to efficiently manage the manufacturing as well as technical domain of complex modules developed by our R&D teamCollaborate with other engineers to ensure a prompt execution as well as efficient and smooth productionTake a lead on driving our suppliers to excellence for enabling smooth manufacturing processes in our facility near MunichYour benefits:An exciting, international, and dynamic environment, working in a high technology company with human touchExtensive further education offers, individual training, learning & development opportunities, and cooperation with experienced employeesCompany pension scheme with the possibility of top-up via salary conversion and disability insuranceTravel insurance, can also be used privatelyCapital-forming benefits (VWL)30 days of vacationBonus programSign up with Urban Sports Club and enjoy the facilitiesFree beverages, fresh seasonal fruits & vegetablesEmployees can enjoy meals at a reduced cost through our cafeteria's subsidized pricingPossibility to work remotelySounds interesting? Then it is best to apply via our online portal. If you have any questions, please do not hesitate to contact me at **********Know more through our YouTube channel! Applied Materials Integrated Circuit Testing GmbH Ammerthalstrasse 20 85551 Heimstetten near Munich www.appliedmaterials.comQualificationsEducation:Bachelor's DegreeSkills:Certifications:Languages:Years of Experience:4 - 7 YearsWork Experience:Additional InformationTime Type:Full timeEmployee Type:Assignee / RegularTravel:Yes, 10% of the TimeRelocation Eligible:YesApplied Materials is an Equal Opportunity Employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, national origin, citizenship, ancestry, religion, creed, sex, sexual orientation, gender identity, age, disability, veteran or military status, or any other basis prohibited by law. Über das Unternehmen:APPLIED MATERIALS

Mit rund 6.000 Mitarbeitern und zahlreichen Produktionsstandorten im In- und Ausland sowie 1,55 Mrd. Euro Umsatz gehören wir zu den führenden Unternehmensgruppen für Farben, Lacke, Bautenschutz und energiesparende Wärmedämm-Verbundsysteme in Europa mit Sitz im Rhein-Main-Gebiet. Im Profi- und auch DIY-Geschäft sind wir mit unseren bekannten Marken Caparol und Alpina Marktführer. Zur Verstärkung unseres Teams Group HSE (Health, Safety, Environment) suchen wir zum nächstmöglichen Zeitpunkt einen HSE Manager* Das erwartet dich: Als Health-Safety-Environment Manager bist du fachliche Ansprechperson für unsere Werkleitung und Gruppenfunktionen, wirst perspektivisch als Störfallbeauftragter bestellt und hast in deiner Funktion einen sehr hohen Gestaltungsspielraum zur Etablierung von Prozessen in unserem Unternehmen. Im Austausch mit Behörden, Anlagenbetreibern und Werkleitung, wirkst du ganzheitlich auf eine Verbesserung der Sicherheit unserer Anlagen hin. Du überwachst die Einhaltung des BImSchG und seiner Verordnungen - auch durch regelmäßige Kontrollen unserer Betriebsanlagen. Du bist für die Erstellung und Fortschreibung immissionsschutzrechtlich relevanter Dokumente verantwortlich (Sicherheitsbericht). Durch dein Fachwissen unterstützt du die Optimierung und Erstellung relevanter Compliance-Prozesse und schulst Führungskräfte. Du identifizierst Änderungsvorhaben mit Genehmigungsrelevanz und arbeitest an der Erstellung der relevanten Antragsunterlagen mit. Das Incident-Reporting am Standort läuft bei dir zusammen. Du informierst bei Vorfällen relevante Stakeholder und führst Statistiken. Das bringst du mit: Du hast ein erfolgreich abgeschlossenes naturwissenschaftliches oder technisches Hochschulstudium (z. B. Ingenieurwesen, Chemie oder Physik) mit einer mindestens zweijährigen Berufserfahrung an technischen Anlagen oder eine vergleichbare technische Fachschulausbildung und einem Meisterabschluss mit mindestens 4 Jahren Berufserfahrung in der Anlagen- und Verfahrenstechnik. Eine Qualifikation zum Störfallbeauftragten wäre von Vorteil. Idealerweise verfügst du über umfassende Kenntnisse der typischen Abläufe und Prozesse eines chemischen Produktionsstandorts. Du bringst Erfahrung im Bereich Anlagensicherheit und Umwelt-Compliance mit. Du verfügst über die ausgezeichnete Fähigkeit, komplexe Sachverhalte sowie technische Abläufe und Zusammenhänge präzise und überzeugend darzustellen und zu präsentieren. Eine strukturierte und eigenverantwortliche Arbeitsweise, diplomatisches Geschick und ein überzeugendes Argumentations- und Durchsetzungsvermögenrunden dein Profil ab. Du kommunizierst fließend in Deutsch und für die internationale Zusammenarbeit fließend in Englisch. We are looking forward to your online application! With around 6,000 employees worldwide, a large number of production locations in Germany and abroad and an achieved turnover of 1.55 billion euros, DAW is today the largest private company in the industry in Europe for innovative coating systems for buildings and building protection, based near Frankfurt. With our famous brands Caparol and Alpina we are market leader in both the professional and the DIY trade.Über das Unternehmen:DAW SE

Overview:Hard Rock International, spirited & authentic, a global brand that continues to expand around the world. Since 1971, passionate and talented business leaders have paved the way for the next generation of Hard Rock Cafe leaders to deliver authentic experiences that rock!Responsibilities:Hard Rock Cafe is seeking a talented Kitchen Manager reporting to the General Manager. Our operators are true entrepreneurs who manage large teams and multi-dimensional operations that encompass fresh, made from scratch ingredients, iconic bars, live music, phenomenal events, and rocking retail operations. This is not just another “job opportunity”. So, the question is, “do you have what it takes to join the band?” Demonstrate financial comprehension of Cafe’s budget and P&L. Effectively control costs of food and related purchases in alignment with budgeted expectations. Manage staff schedules in accordance with the cafe’s budget and forecast models. Maintain the highest standards of brand, local health, safety, and food preparation hygiene requirements. Support the team in consistent execution of all systems and processes to consistently deliver all products and services to brand standards. Support senior management in building a highly functional hourly team who share a common vision and values surrounding the overall success of the Cafe. Develop kitchen team in all aspects of kitchen execution from 100% recipe adherence to banquet service. Foster an environment of customer service in which all team members put the guest first in every situation. Execute established food standards for overall guest satisfaction that meet or exceed brand standards. Ensure the highest levels of hygiene and food handling practices to deliver optimal quality of product to guests. Attract and retain the most exceptionally talented culinary talent available in the market and place them in positions that leverage their skills and expertise for maximum impact. Clearly define goals and expectations for Heart of House hourly team members using performance review tools and hold your people accountable for successful performance. Support staff development and advancement along well-defined career paths. Manage a diverse team ensuring a balanced and proactive approach to increasing individual potential across the team. Serve as a Culinary Learning Coach developing, implementing, and executing learning & development programs for all Heart of House employees in order to drive continuous improvement and employee retention. Possess a self-motivated approach to his/her own personal and professional growth.Qualifications:Got What It Takes To Be In The Band?Relevant experience in the hospitality industry inclusive of restaurant culinary operationsPossess all local food management and safety certificationsAbility to learn and bring "out of the box" ideas to their teamGenuine enthusiasm and aptitude for foodExcellent verbal and written communication skillsHigh level of business acumen and common senseDemonstrates strong problem solving skills through ability to diagnose and implement solutionsMust possess strong communication and listening skills, excellent speaking, reading and writing.Comprehend and use technical or professional language, either written or spoken, to communicate complex ideas.Ability to effectively pitch and present information in one-on-one and group situations to media, customers, clients, partners and other employees of the organization.Multiple language abilities a plus, fluency in English required.Must have a valid EU work permit to work in this location.Please submit CV/Resume in English. #IndeedEUÜber das Unternehmen:Hard Rock International (USA), Inc.

WER WIR SIND. Wir sind ein multikulturelles internationales Unternehmen mit viel Teamspirit. Mit 500 Mitarbeiter*innen in 5 Ländern arbeiten wir daran, für kommende Generationen eine klimafreundliche Energieerzeugung sicherzustellen. Wir bauen Freiflächen-Solarkraftwerke in ganz Europa und sichern als einer der weltweit größten O&M-Dienstleister den jahrzehntelangen Anlagenbetrieb unserer Kunden. Der Schutz des Klimas sowie die kostengünstige und sichere Energieversorgung sind unser Ziel. Wir fördern die Akzeptanz von Solarenergie und tragen somit zum Gelingen der Energiewende bei. Für die nächsten Generationen werden wir die Welt ein Stückchen besser machen. Ob Kolitzheim, Berlin oder Nürnberg – neben unserem Hauptsitz in Kolitzheim bieten wir auch Jobs in unserem Hauptstadtbüro und an unseren Co-Working-Standorten sowie mobiles Arbeiten. Project Quality Manager Renewables (m/w/d) Vollzeit | Berlin, Kolitzheim, Nürnberg | Quality Management DEINE AUFGABEN. Qualitätsmanagement ist deine Leidenschaft. Du entwickelst gerne Prozesse und arbeitest mit Freude im Team. Bewirb dich jetzt und werde Teil unseres Teams! Entwicklung und Überarbeitung des Qualitätsprozesses in Zusammenarbeit mit Supplier Quality Manager (m/w/d) und dem Projektmanagement Unterstützung des Sales-Teams im Vorfeld mit den Standard-Belectric-Qualitätsanforderungen Unterstützung bei der Durchführbarkeit der Qualitätsanforderungen des Kunden und dem dazugehörigen Qualitätsbudget für die Projekte Festlegung von Qualitätsanforderungen für unsere Subunternehmer und deren Schulung zu unseren Qualitätsstandards Erstellung des Projektqualitätsplans und Einrichtung des Qualitätskontrollsystems in PlanRadar für die Projekte NCR-Management: Analyse von internen und externen Nichtkonformitäten (NCRs), Ursachenanalyse und Umsetzung von Korrektur- und Vorbeugungsmaßnahmen Unterstützung und Koordination zwischen Supplier Quality Manager (m/w/d) und dem Projektteam bei Qualitätsproblemen Qualifizierung neuer Subunternehmer in Abstimmung mit dem zugehörigen Category Manager (m/w/d) aus dem Team Supply Chain & Procurement Qualitätsschulung für Projektteams und Subunternehmer DEIN PROFIL. Abgeschlossene kaufmännische oder technische Berufsausbildung, abgeschlossenes Studium aus dem Bereich Qualität- bzw. Bauingenieurwesen oder vergleichbare Qualifikation Mehrjährige Berufserfahrung im Qualitätsmanagement im Bereich Construction oder Baustellenmanagement gerne im internationalen Umfeld Erfahrung im Umgang mit Nichtkonformitäten (NCR), Ursachenanalyse und den damit verbundenen Qualitätskosten Sehr gute Kenntnisse in MS Office Nice to have: Erfahrung mit PlanRadar, Jira, Confluence Sehr gute Deutsch- und Englischkenntnisse (mindestens C1) Deine Skills: lösungsorientierter Teamplayer (m/w/d) mit sehr guten kommunikativen Fähigkeiten, ein gutes Auge fürs Detail sowie Verhandlungskompetenz und interkultureller Kompetenz Reisebereitschaft bis max. 30 % Führerschein Klasse B DAS BIETEN WIR DIR. Jobs für (d)eine grüne Zukunft. Flache Hierarchien mit guten Entwicklungsmöglichkeiten. Unbefristete Arbeitsverträge. Ein familiäres und kollegiales Miteinander im internationalen Umfeld. Flexible Arbeitszeiten und mobiles Arbeiten. JobRad-Leasing. Vermögenswirksame Leistungen und betriebliche Altersvorsorge. Regelmäßige Mitarbeiterevents. Neugierig? Mobiles Arbeiten Flexible Arbeitsmodelle BELECTRICAcademy VWL &Betriebliche Altersvorsorge UnbefristeteArbeitsverträge 30 Tage Urlaub Jobrad-Leasing Parkplätze für Mitarbeiter Kostenfreies Laden für E-Autos Mitarbeitervorteile Team-Events & Gesundheitstag Kantine, Obst & Getränke DEIN WEG ZU UNS. Du hast Fragen? Ruf uns gerne an – dein Recruiting Team Klara Theobald und Melanie Adolph unter +49 9385 548-9184 oder -9246. Oder bewirb dich gleich, am besten über unser Onlineportal. All unsere Vorteile findest du unter belectric.com/karriere. BELECTRIC GmbHWadenbrunner Str. 10 | 97509 KolitzheimMauerstraße 77 | 10117 BerlinStraße des Friedens 15 | 14943 LuckenwaldeOhmstraße 19 | 97076 Würzburg (Co-Working-Space)Bahnhofstraße 2 | 90402 Nürnberg (Co-Working-Space) ********** | www.belectric.com JOBS FOR FUTURE. STANDORTE. UNTERNEHMENSGRÖSSE 500 Mitarbeitende in 5 Ländern BRANCHE Energie-/Wasserversorgung WEBSITE www.belectric.com Über das Unternehmen:Belectric GmbHBranche:Energie-/Wasserversorgung

Momentaufnahme von Ihrem Tag Als Teammitglied unterstützen Sie Dienstleistungsprojekte in allen Einkaufsthemen. Einige davon setzen Sie eigenständig um, andere werden innerhalb der Siemens Energy Organisation bearbeitet. Sie steuern und beraten Schnittstellen wie PM bei komplexen Anforderungen von Projekten im Hinblick auf die Geschäftsziele einschließlich Budget, Qualität und Termintreue.Wie Sie etwas bewirken können Teilnahme an internen Projektbesprechungen gefolgt von anschließendem ermitteln, analysieren und weiterleiten der Beschaffungsbedarfe Beratung interner Stakeholder zu den besten Beschaffungsoptionen und Sicherstellung der Umsetzung - Fungieren als zentrale Anlaufstelle für ausgewählte ProjekteProaktive Implementierung und Umsetzung des Early-Involvement-EinkaufskonzeptsEntwicklung einer Vergabestrategie unter Berücksichtigung von Projektzielen, Kosten und Qualität sowie Präsentation des Gesamtkostenvergleichs im Sourcing Board und dessen UmsetzungVorbereitung und Durchführung von Vertragsverhandlungen unter Anwendung der verfügbaren Beschaffungshebel (eANC, etc.) zur Erzielung von Best-in-Class ErgebnissenFestlegung der Strategie basierend auf den Bedürfnissen der Geschäftseinheit - Lieferantenentwicklungsplan in enger Zusammenarbeit mit SQM, CVE & Global Commodity ManagementEnge Zusammenarbeit und Austausch mit internen und externen Stakeholdern weltweitWas Sie mitbringen Hochschulabschluss bevorzugt mit ingenieurwissenschaftlichem Hintergrund oder BWL mit starker Affinität zur TechnikLangjährige erfolgreiche Berufserfahrung im BeschaffungswesenKomplexe Kenntnisse der grundlegenden Konzepte, Praktiken und Verfahren der ProjektbeschaffungHervorragende soziale Managementfähigkeiten: aktives Zuhören, Zusammenarbeit, Kommunikation, Überzeugungskraft und ServiceorientierungFließende Beherrschung der englischen und deutschen Sprach, eine weitere Fremdsprache ist wünschenswertFortgeschrittene Kenntnisse der MS-Office-Anwendungen, SAP, ARIBA Gas Services Emissionsarme Stromerzeugung durch Technologie, Lösungen, Service und Dekarbonisierung. Wir verbessern und optimieren die konventionelle und erneuerbare Energieversorgung. Dadurch können wir unsere Energiequellen optimal nutzen, um die Energiewende zu unterstützen. Wer ist Siemens Energy? Wir bei Siemens Energy sind mehr als nur ein Energietechnologieunternehmen. Wir decken den wachsenden Energiebedarf in über 90 Ländern und sorgen dabei für den Schutz unseres Klimas. Mit über 94.000 engagierten Mitarbeitern erzeugen wir nicht nur Elektrizität für über 16 % der Weltbevölkerung, sondern setzen unsere Technologie auch für den Schutz von Mensch und Umwelt ein. Unser globales Team engagiert sich dafür, nachhaltige, zuverlässige und erschwingliche Energie Wirklichkeit werden zu lassen, indem es die Grenzen des Möglichen immer weiter ausdehnt. Wir blicken stolz auf unser 150-jähriges Erbe der Innovation zurück, das uns ermutigt, nach Menschen zu suchen, die unseren Fokus auf die Reduzierung von CO2, neue Technologien und Energiewende unterstützen. Erfahren Sie mehr darüber, wie Sie bei Siemens Energy etwas bewegen können: https://bitly.ws/ZFwV Unser Engagement für Vielfalt Gut, dass wir nicht alle gleich sind. Vielfalt macht uns leistungsstark. Wir leben von Inklusion und unsere gemeinsame kreative Energie wird von über 130 Nationalitäten gespeist. Siemens Energy setzt auf den Charakter - unabhängig von ethnischem Hintergrund, Geschlecht, Alter, Religion, Identität oder Behinderung. Wir versorgen die Gesellschaft mit Energie - die ganze Gesellschaft - und wir diskriminieren nicht aufgrund von Unterschieden, die zwischen uns bestehen. Benefits Neben einem attraktiven, marktgerechten Vergütungspaket erwartet Sie eine attraktive arbeitgeberfinanzierte betriebliche AltersversorgungDaneben bieten wir die Möglichkeit, zu sehr interessanten Mitarbeiterkonditionen Aktionär*in von Siemens Energy zu werdenUnter unserem Motto #BetterTogether bieten wir unseren Mitarbeitenden die Möglichkeit, flexibel und auch remote zu arbeiten. Aber auch unsere Büros lassen keine Wünsche offen und bieten Raum für inspirierende Zusammenarbeit und KreativitätDie berufliche und auch persönliche Weiterentwicklung unserer Mitarbeitenden ist uns ein großes Anliegen. Sie haben bei uns die Möglichkeit selbstbestimmt zu lernen und sich zu entwickeln. Dafür stehen unterschiedliche attraktive Programme und Maßnahmen zur VerfügungUnter dem Aspekt "Vereinbarkeit von Familie und Beruf" haben wir ein vielfältiges Angebot, z.B. flexible Arbeitszeitmodelle, Kinderbetreuungsplätze an vielen Standorten, die Möglichkeit zur Schnupperteilzeit oder auch ein Sabbatical Wir legen Wert auf Chancengleichheit und freuen uns über Bewerbungen von Menschen mit Behinderung. https://jobs.siemens-energy.com/jobs Über das Unternehmen:Siemens Energy

Job Description We are looking for a dedicated, experienced Construction Instrumentation and Control QAQC Manager to join us in our mission to contribute to a greener future. The role is a part of our excellent Construction Quality Site team based in Skellefteå (Sweden). By joining us, you will be a key player in establishing a sound QAQC Site team and will contribute to building one of the first large scale European battery factories. About the jobBe an Instrumentation and Control focal Point for QAQC matters for site projects, and facilities development. Responsible for developing implementing, auditing and monitoring project QAQC Plan and programs in compliance Company Specifications, applicable International Codes and Standards, and local Swedish Standards will be also a plus. Ensure that plants and factory facilities are constructed according to Company and Project Specifications, design documents, applicable codes and standards and acceptable work practices.About the teamJoin us to work into an international environment team of more than 151 nationalities, based in the north of Sweden, where an active QAQC team is rapidly growing to achieve great goals set for 2025. The candidate will contribute to the implementation of a QAQC system along with his team, amongst all site contractors and subcontractors to turn green battery factory in a tangible reality. Key responsibilities include but are not limited to:Develop and maintain Project Quality Plans for the different projectsSet up and develop QAQC procedures, ITP, quality management systems to effectively monitor QAQC performance, review and approve ITP's, ITR'S and all formal documentation, report KPI, support project activities with EPC contractorsWorking alongside Swedish personnel and understanding the Swedish codes of practiceEnsuring quality assurance of all work scopes is maintained and all work is performed in accordance with company policies and the Health & Safety at work actTo coordinate the establishment, implementation and, maintenance of the Project inspection and test programs and associated witness point(s) time schedule on a system-by-system basisTakes the lead on resolving all Non-conformance Reports (NCR’s) and Corrective Action Requests (CARs), with an emphasis on investigating root cause analysis, identifying trends, and driving improvementsPersonal success factors:The person we are looking for is driven, caring and structuredYou thrive by leading others and work towards common goalsYou are used to a high paced work environment and got good time management skillsQualities that we cherish are flexibility, sense of quality, friendliness, motivation to take on new challenges, grit and a sense of humourNorthvolt is an equal opportunity employer. We're a diverse group of individuals, united by a common mission, who recognise that while our actions as individuals have a role to play in driving Northvolt towards its goals, we always seek to move forward as a team. We offer you an open and welcoming atmosphere where we win as a team – and fail as a team. Northvolt is growing at the speed of light and we are a strong believer in internal career development. For us it’s important to look at your skills and potential, please refrain form including your picture and age with your application to help us with this.Apply with CV in English or your complete LinkedIn profile. Full time employment, fixed salary. Planned starting date is ASAP.

Process Manager:in Digitalization (m|w|d) (Business IT Specialist (Fachschule)) Programmed for good ideas: GTE Industrieelektronik is a growing technology company based in Viersen, Germany. As experts in sensor-based safety technology, we develop and produce innovative products in the fields of measurement, control and fire detection technology. We have been a reliable partner for our customers and employees for over 35 years. Processes, IT & QM: the task You are responsible for providing the process landscape in the company and mapping it to the company IT. Our company is dynamic. You continuously analyze our business processes and ensure optimal support through functional IT solutions. You support the head of quality management in the technical implementation of the quality policy and in compliance with and documentation of the specifications in accordance with ISO9001. IT-savvy & analytical: your profile Training as a business IT specialist, digitalization management specialist or technical training; alternatively a technical/scientific degree or comparable qualification Knowledge of ISO9001 Experience in IT and databases Strong analytical skills and independent working style Collegial & with a strong future: the working environment Secure and attractive workplace Motivating working atmosphere Flat hierarchy Individual development opportunities Comprehensive benefits package with pension and health benefits Welcome to the team: the key data Start: immediately or by arrangement Scope: full-time (part-time possible) Department: Quality management Location: 41747 Viersen Mobile working possible at times The working environment at GTE is characterized by a collegial team, trust in the skills of the employees and freedom for personal development opportunities. Career starters are just as welcome as employees with a wealth of experience. We look forward to receiving your detailed application stating your desired salary and earliest possible starting date at [email protected] (contact: Wolfgang Mu00fchge or Judith Laurs). We only process application attachments in PDF format

Polyethylene/Polypropylene Compounding Recycling, Circularity and SustainabilityRemote position: option for person to be based in Germany, Hungary, Italy, Austria, Czech Republic, Poland, Slovakia, Slovenia, Serbia or RomaniaJob ref: CST /59450Salary/Benefits: Attractive based on experienceThe Company:Our client is an integrated, international oil and gas company. It is active in over 30 countries with a dynamic international workforce of 25,000 people and a track record of more than 80 years in the industry. They are committed to doing business responsibly and sustainably, supporting communities and striving to meet the best possible health, safety and security standards wherever it operates. A key part of this strategy is further expanding its polymer compounding business with a strong commitment to recycling technologies.Purpose of Role:The Group DS Circular Chemicals Recycling Marketing Manager is responsible for P&L of polyolefin recycling business as well as related market development programs, in order to create new, profitable and growing sustainable chemical portfolio and support sustainability goals of the Downstream division.It defines and supervises the execution of the business plan for polyolefin recycling in line with the strategic directions for Downstream circular chemicals. Leads the Recycling business team to reach the strategic targets.Responsibilities:Define the business plan, oversee the business opportunities (new product development, testing, customer trials, negotiation).Set marketing strategy for polyolefin recycling business line, define priorities for targeted applications, pricing strategies and Value Propositions. Leads value focused market development, provides direction and toolset to the sales team, directs sales pipeline priorities.Drives products' awareness at potential customers, industry influencers, builds industry network and develops best practices.Identifies profitability drivers and proposes actions and mid- and long term strategies to address it. Responsible for screening the ‘market and make’ proposals for inorganic targets.Accountable for market part of business cases to support the Organic & Inorganic Investments and actively involved in due diligence to enable growth of the recycling business line.Direct and support Recycling Sales Head at Chemical Business Unit to build, manage and develop customer base (strategic pipeline) in order to ensure smooth and fast market entry and to reach targeted market shares in line with strategic plans.Runs Market Intelligence on product applications and European regulations related to the product applications. Integrates market and technical information to suggest new ideas for development steps.Supervise market developers. Collaborate closely with other DS and MOL Group departments, especially with Chemical Business Unit and Circular Economy Services as well as with External Partners to enable growth of the business line.Manages his/her business team with ownership, ensures sustainable solutions and customer focused operation. Responsible for the development and succession of his/her subordinates.Responsible for ensuring and controlling of compliance with the related legal and company rules - with special regard to the general regulations defining company operation: Code of Ethics and Business Conduct, rules of Conflict of Interest, HSE and Data Protection.The Person:MSc degree in Economics/ Business Management/ Engineering8-10 years relevant professional experience working within plastic/polymer/packaging industry. Additional knowledge of recycling is an advantageKnowledge of polymers (product and process)Proven working experience in international environmentKnowledge of sales process and pipeline managementValue selling skills and active listeningFluent in EnglishProfessional competencies:Customer FocusTeam leadershipBusiness AcumenMarketplace insightCommunicationRisk AssessmentDecision MakingFor reasons of better legibility, the simultaneous use of the language forms male, female and diverse (f/m/d) is avoided. All personal designations apply equally to all genders.For EU roles, candidates must be eligible to work and live in the European Union. Proof of eligibility will be required with your application.To apply please contact Conrad TaylorE-Mail anzeigenWhy select Listgrove?Established in 1975Recruited in 68 countriesRecognised International brandGlobal network of Clients and candidatesJoin over 80,000 professionals from the plastics, packaging, petrochemicals, chemicals, energy and recycling sectors by following us on LinkedIn. www.linkedin.com/company/listgrove-limitedTHROUGHOUT 2023 & 2024 YOU CAN ALSO MEET WITH LISTGROVE AT THE FOLLOWING EXHIBITIONS:PLAST 2023 Milan Italy, Kunststoffenbeurs's-Hertogenbosch The Netherlands,Interplas Birmingham UK, NPE Orlando USARecruiting business leaders and functional specialists with the skills and knowledge to deliver a sustainable future.Performance through PeoplePlease visit www.listgrove.com for more information on our services, global success and testimonials.Listgrove Limited Registered in England No: 01197713 Standort Listgrove Ltd, Düsseldorf

Polyethylene/Polypropylene Compounding Recycling, Circularity and SustainabilityRemote position: option for person to be based in Germany, Hungary, Italy, Austria, Czech Republic, Poland, Slovakia, Slovenia, Serbia or RomaniaJob ref: CST /59450Salary/Benefits: Attractive based on experienceThe Company:Our client is an integrated, international oil and gas company. It is active in over 30 countries with a dynamic international workforce of 25,000 people and a track record of more than 80 years in the industry. They are committed to doing business responsibly and sustainably, supporting communities and striving to meet the best possible health, safety and security standards wherever it operates. A key part of this strategy is further expanding its polymer compounding business with a strong commitment to recycling technologies.Purpose of Role:The Group DS Circular Chemicals Recycling Marketing Manager is responsible for P&L of polyolefin recycling business as well as related market development programs, in order to create new, profitable and growing sustainable chemical portfolio and support sustainability goals of the Downstream division.It defines and supervises the execution of the business plan for polyolefin recycling in line with the strategic directions for Downstream circular chemicals. Leads the Recycling business team to reach the strategic targets.Responsibilities:Define the business plan, oversee the business opportunities (new product development, testing, customer trials, negotiation).Set marketing strategy for polyolefin recycling business line, define priorities for targeted applications, pricing strategies and Value Propositions. Leads value focused market development, provides direction and toolset to the sales team, directs sales pipeline priorities.Drives products' awareness at potential customers, industry influencers, builds industry network and develops best practices.Identifies profitability drivers and proposes actions and mid- and long term strategies to address it. Responsible for screening the ‘market and make’ proposals for inorganic targets.Accountable for market part of business cases to support the Organic & Inorganic Investments and actively involved in due diligence to enable growth of the recycling business line.Direct and support Recycling Sales Head at Chemical Business Unit to build, manage and develop customer base (strategic pipeline) in order to ensure smooth and fast market entry and to reach targeted market shares in line with strategic plans.Runs Market Intelligence on product applications and European regulations related to the product applications. Integrates market and technical information to suggest new ideas for development steps.Supervise market developers. Collaborate closely with other DS and MOL Group departments, especially with Chemical Business Unit and Circular Economy Services as well as with External Partners to enable growth of the business line.Manages his/her business team with ownership, ensures sustainable solutions and customer focused operation. Responsible for the development and succession of his/her subordinates.Responsible for ensuring and controlling of compliance with the related legal and company rules - with special regard to the general regulations defining company operation: Code of Ethics and Business Conduct, rules of Conflict of Interest, HSE and Data Protection.The Person:MSc degree in Economics/ Business Management/ Engineering8-10 years relevant professional experience working within plastic/polymer/packaging industry. Additional knowledge of recycling is an advantageKnowledge of polymers (product and process)Proven working experience in international environmentKnowledge of sales process and pipeline managementValue selling skills and active listeningFluent in EnglishProfessional competencies:Customer FocusTeam leadershipBusiness AcumenMarketplace insightCommunicationRisk AssessmentDecision MakingFor reasons of better legibility, the simultaneous use of the language forms male, female and diverse (f/m/d) is avoided. All personal designations apply equally to all genders.For EU roles, candidates must be eligible to work and live in the European Union. Proof of eligibility will be required with your application.To apply please contact Conrad TaylorE-Mail anzeigenWhy select Listgrove?Established in 1975Recruited in 68 countriesRecognised International brandGlobal network of Clients and candidatesJoin over 80,000 professionals from the plastics, packaging, petrochemicals, chemicals, energy and recycling sectors by following us on LinkedIn. www.linkedin.com/company/listgrove-limitedTHROUGHOUT 2023 & 2024 YOU CAN ALSO MEET WITH LISTGROVE AT THE FOLLOWING EXHIBITIONS:PLAST 2023 Milan Italy, Kunststoffenbeurs's-Hertogenbosch The Netherlands,Interplas Birmingham UK, NPE Orlando USARecruiting business leaders and functional specialists with the skills and knowledge to deliver a sustainable future.Performance through PeoplePlease visit www.listgrove.com for more information on our services, global success and testimonials.Listgrove Limited Registered in England No: 01197713 Standort Listgrove Ltd, Hamburg

Polyethylene/Polypropylene Compounding Recycling, Circularity and SustainabilityRemote position: option for person to be based in Germany, Hungary, Italy, Austria, Czech Republic, Poland, Slovakia, Slovenia, Serbia or RomaniaJob ref: CST /59450Salary/Benefits: Attractive based on experienceThe Company:Our client is an integrated, international oil and gas company. It is active in over 30 countries with a dynamic international workforce of 25,000 people and a track record of more than 80 years in the industry. They are committed to doing business responsibly and sustainably, supporting communities and striving to meet the best possible health, safety and security standards wherever it operates. A key part of this strategy is further expanding its polymer compounding business with a strong commitment to recycling technologies.Purpose of Role:The Group DS Circular Chemicals Recycling Marketing Manager is responsible for P&L of polyolefin recycling business as well as related market development programs, in order to create new, profitable and growing sustainable chemical portfolio and support sustainability goals of the Downstream division.It defines and supervises the execution of the business plan for polyolefin recycling in line with the strategic directions for Downstream circular chemicals. Leads the Recycling business team to reach the strategic targets.Responsibilities:Define the business plan, oversee the business opportunities (new product development, testing, customer trials, negotiation).Set marketing strategy for polyolefin recycling business line, define priorities for targeted applications, pricing strategies and Value Propositions. Leads value focused market development, provides direction and toolset to the sales team, directs sales pipeline priorities.Drives products' awareness at potential customers, industry influencers, builds industry network and develops best practices.Identifies profitability drivers and proposes actions and mid- and long term strategies to address it. Responsible for screening the ‘market and make’ proposals for inorganic targets.Accountable for market part of business cases to support the Organic & Inorganic Investments and actively involved in due diligence to enable growth of the recycling business line.Direct and support Recycling Sales Head at Chemical Business Unit to build, manage and develop customer base (strategic pipeline) in order to ensure smooth and fast market entry and to reach targeted market shares in line with strategic plans.Runs Market Intelligence on product applications and European regulations related to the product applications. Integrates market and technical information to suggest new ideas for development steps.Supervise market developers. Collaborate closely with other DS and MOL Group departments, especially with Chemical Business Unit and Circular Economy Services as well as with External Partners to enable growth of the business line.Manages his/her business team with ownership, ensures sustainable solutions and customer focused operation. Responsible for the development and succession of his/her subordinates.Responsible for ensuring and controlling of compliance with the related legal and company rules - with special regard to the general regulations defining company operation: Code of Ethics and Business Conduct, rules of Conflict of Interest, HSE and Data Protection.The Person:MSc degree in Economics/ Business Management/ Engineering8-10 years relevant professional experience working within plastic/polymer/packaging industry. Additional knowledge of recycling is an advantageKnowledge of polymers (product and process)Proven working experience in international environmentKnowledge of sales process and pipeline managementValue selling skills and active listeningFluent in EnglishProfessional competencies:Customer FocusTeam leadershipBusiness AcumenMarketplace insightCommunicationRisk AssessmentDecision MakingFor reasons of better legibility, the simultaneous use of the language forms male, female and diverse (f/m/d) is avoided. All personal designations apply equally to all genders.For EU roles, candidates must be eligible to work and live in the European Union. Proof of eligibility will be required with your application.To apply please contact Conrad TaylorE-Mail anzeigenWhy select Listgrove?Established in 1975Recruited in 68 countriesRecognised International brandGlobal network of Clients and candidatesJoin over 80,000 professionals from the plastics, packaging, petrochemicals, chemicals, energy and recycling sectors by following us on LinkedIn. www.linkedin.com/company/listgrove-limitedTHROUGHOUT 2023 & 2024 YOU CAN ALSO MEET WITH LISTGROVE AT THE FOLLOWING EXHIBITIONS:PLAST 2023 Milan Italy, Kunststoffenbeurs's-Hertogenbosch The Netherlands,Interplas Birmingham UK, NPE Orlando USARecruiting business leaders and functional specialists with the skills and knowledge to deliver a sustainable future.Performance through PeoplePlease visit www.listgrove.com for more information on our services, global success and testimonials.Listgrove Limited Registered in England No: 01197713 Standort Listgrove Ltd, Leipzig

Polyethylene/Polypropylene Compounding Recycling, Circularity and SustainabilityRemote position: option for person to be based in Germany, Hungary, Italy, Austria, Czech Republic, Poland, Slovakia, Slovenia, Serbia or RomaniaJob ref: CST /59450Salary/Benefits: Attractive based on experienceThe Company:Our client is an integrated, international oil and gas company. It is active in over 30 countries with a dynamic international workforce of 25,000 people and a track record of more than 80 years in the industry. They are committed to doing business responsibly and sustainably, supporting communities and striving to meet the best possible health, safety and security standards wherever it operates. A key part of this strategy is further expanding its polymer compounding business with a strong commitment to recycling technologies.Purpose of Role:The Group DS Circular Chemicals Recycling Marketing Manager is responsible for P&L of polyolefin recycling business as well as related market development programs, in order to create new, profitable and growing sustainable chemical portfolio and support sustainability goals of the Downstream division.It defines and supervises the execution of the business plan for polyolefin recycling in line with the strategic directions for Downstream circular chemicals. Leads the Recycling business team to reach the strategic targets.Responsibilities:Define the business plan, oversee the business opportunities (new product development, testing, customer trials, negotiation).Set marketing strategy for polyolefin recycling business line, define priorities for targeted applications, pricing strategies and Value Propositions. Leads value focused market development, provides direction and toolset to the sales team, directs sales pipeline priorities.Drives products' awareness at potential customers, industry influencers, builds industry network and develops best practices.Identifies profitability drivers and proposes actions and mid- and long term strategies to address it. Responsible for screening the ‘market and make’ proposals for inorganic targets.Accountable for market part of business cases to support the Organic & Inorganic Investments and actively involved in due diligence to enable growth of the recycling business line.Direct and support Recycling Sales Head at Chemical Business Unit to build, manage and develop customer base (strategic pipeline) in order to ensure smooth and fast market entry and to reach targeted market shares in line with strategic plans.Runs Market Intelligence on product applications and European regulations related to the product applications. Integrates market and technical information to suggest new ideas for development steps.Supervise market developers. Collaborate closely with other DS and MOL Group departments, especially with Chemical Business Unit and Circular Economy Services as well as with External Partners to enable growth of the business line.Manages his/her business team with ownership, ensures sustainable solutions and customer focused operation. Responsible for the development and succession of his/her subordinates.Responsible for ensuring and controlling of compliance with the related legal and company rules - with special regard to the general regulations defining company operation: Code of Ethics and Business Conduct, rules of Conflict of Interest, HSE and Data Protection.The Person:MSc degree in Economics/ Business Management/ Engineering8-10 years relevant professional experience working within plastic/polymer/packaging industry. Additional knowledge of recycling is an advantageKnowledge of polymers (product and process)Proven working experience in international environmentKnowledge of sales process and pipeline managementValue selling skills and active listeningFluent in EnglishProfessional competencies:Customer FocusTeam leadershipBusiness AcumenMarketplace insightCommunicationRisk AssessmentDecision MakingFor reasons of better legibility, the simultaneous use of the language forms male, female and diverse (f/m/d) is avoided. All personal designations apply equally to all genders.For EU roles, candidates must be eligible to work and live in the European Union. Proof of eligibility will be required with your application.To apply please contact Conrad TaylorE-Mail anzeigenWhy select Listgrove?Established in 1975Recruited in 68 countriesRecognised International brandGlobal network of Clients and candidatesJoin over 80,000 professionals from the plastics, packaging, petrochemicals, chemicals, energy and recycling sectors by following us on LinkedIn. www.linkedin.com/company/listgrove-limitedTHROUGHOUT 2023 & 2024 YOU CAN ALSO MEET WITH LISTGROVE AT THE FOLLOWING EXHIBITIONS:PLAST 2023 Milan Italy, Kunststoffenbeurs's-Hertogenbosch The Netherlands,Interplas Birmingham UK, NPE Orlando USARecruiting business leaders and functional specialists with the skills and knowledge to deliver a sustainable future.Performance through PeoplePlease visit www.listgrove.com for more information on our services, global success and testimonials.Listgrove Limited Registered in England No: 01197713 Standort Listgrove Ltd, Essen

Übernehme eine entscheidende Rolle dabei, das Leben für chronische Schmerzpatient:innen positiv zu beeinflussen und eine hochinnovative Lösung für die Indikation Neurologie / Schmerz zu entwickeln. Unser Kunde ist ein internationales mittelständisches Biopharmaunternehmen mit Sitz im Großraum München, das vor dem Launch einer bahnbrechenden Therapie steht und somit seit 30 Jahren die erste grundlegende Innovation auf den Markt bringen möchte.AufgabenDu sorgst dafür, dass die klinischen Studien immer den gesetzlichen Sicherheitsvorgaben entsprechenArbeite mit Dienstleister:innen und Prüfärzt:innen zusammen, um Adverse Events und Protokollabweichungen zu bewerten und zu meldenAls Experte für Sicherheit und medizinisches Monitoring entwickelst du Pläne, um sicherzustellen, dass die Patient:innen sicher und wohl betreut sindDu durchforstest regelmäßig unsere Daten, um potenzielle Sicherheitsprobleme zu identifizieren und zu lösenQualifikationErfolgreich abgeschlossenes MedizinstudiumErste Erfahrungen in der klinischen Forschung und im Umgang mit Datenmanagement-Systemen wünschenswertDeine präzise Arbeitsweise und deine analytischen Fähigkeiten zeichnen dich aus.Kommunikationsstärke und die Fähigkeit, komplexe Sachverhalte verständlich zu präsentieren, sind für diese Position wichtig.Du sprichst gut Deutsch und Englisch und eine der beiden Sprachen fließend.BenefitsAls wertvolles Mitglied in einem hochmotivierten und jungen Team bekommst du die Möglichkeit, schnell viel Verantwortung zu übernehmen und neue Ideen einzubringenGenieße eine moderne Unternehmenskultur, die von einer positiven Fehlerkultur, kurzen Entscheidungswegen und offener Kommunikation geprägt ist. Bei unserem Kunden zählen Ideen und Initiative, nicht Hierarchien.Entspanne dich auf der sonnigen Dachterrasse und stärke den Teamgeist bei zahlreichen Firmenevents, die für Abwechslung und Zusammenhalt sorgen.Wir bieten dir einen familienfreundlichen Job mit geregelten Arbeitszeiten und der Möglichkeit, regelmäßig remote zu arbeiten, damit du Beruf und Privatleben in Einklang bringen kannst.Bewerbungsinformationen:Kopani Consulting GmbH ist eine Personalberatung mit über zehn Jahren Erfahrung in der Rekrutierung und Beratung von Spezialist:innen und Führungskräften aus der Pharmaindustrie und Medizintechnikbranche. Aufgrund dieser Erfahrung können wir Fachexpert:innen und Kund:innen individuell und diskret unterstützen. Schicke uns bitte Deine aussagekräftigen Bewerbungsunterlagen inkl. Gehaltswunsch und frühestmöglichem Starttermin an Maximilian Richter. Tel.: +49 89 2870 24412Du suchst eine andere Stelle?Gerne beraten wir Dich kostenlos hinsichtlich weiterer Top-Positionen. Du erhältst von uns einen vollumfänglichen Überblick der Branche, einen Benchmark zu Deinem Gehalt sowie weitere Möglichkeiten zur fachlichen und persönlichen Weiterentwicklung.Wir, Kopani Consulting, sind eine Personalberatung spezialisiert in Life Science. Unser Fokus liegt auf der pharmazeutischen Industrie sowie der Medizintechnik Branche. Unser absolutes Alleinstellungsmerkmal ist die Zusammenführung von qualifizierten Fachkräften und den passenden Unternehmen. Damit sind wir seit 2017 sehr erfolgreich am Markt vertreten. Wir arbeiten mit vielen unterschiedlichen Unternehmen zusammen, von Big Playern bis hin zu interessanten Mittelständlern sowie Familiengeführten Unternehmen. Standort Kopani Consulting GmbH, Munich

Job Description Do you have experience in leadership within occupational health and safety? Right now, we are actively searching for a manager to join our team at Northvolt ETT in Skellefteå! By working with us, you'll have the opportunity to contribute to the construction of one of Europe's first large-scale battery factories, as well as the electrification and transition to a society free from carbon dioxide emissions. As the head of our Health and Safety department, you will be responsible for establishing our processes and goals, as well as developing a culture around and ensuring safe work practices in our factory. This role will offer you the chance to work both operationally and strategically within our leadership team for Health and Safety. You will lead, coach, and build your team, consisting of Health and Safety engineers, where together you will work to establish our work environment at Northvolt ETT in Skellefteå.Responsibilities:Lead and coach the Health and Safety teamImplement plans, routines, and processes for Health and Safety throughout the factoryDevelop management systems for Health and SafetyBe part of and support operational/daily workLead and support in setting up and complying with requirements and regulations from external and internal needsLead investigations/root cause analysis in incidents. Report successes, issues, and statisticsCoach and train managers and employees to strengthen our Health and Safety culture

Weitere InformationenDie Einstellung erfolgt im Beschäftigtenverhältnis.Die Stelle ist zum nächstmöglichen Zeitpunkt zu besetzen und befristet auf 3 Jahre.Eine Verlängerung von mindestens einem Jahr ist vorgesehen.Die befristete Beschäftigung erfolgt im Rahmen der Befristungsmöglichkeiten des Wissenschaftszeitvertragsgesetzes.Es handelt sich um eine Vollzeitstelle.Eine Promotionsmöglichkeit besteht.Die Eingruppierung richtet sich nach dem TV-L.Die Stelle ist bewertet mit EG 13 TV-L.Unser ProfilAn unserem innovativen Lehrstuhl erarbeiten wir aktuelles Know-how im Bereich der Komponenten der Elektromobilität. Im Rahmen unserer nationalen und internationalen Industrie- und Forschungsvorhaben vermitteln wir neben dem Projektmanagement auch ausgezeichnete Präsentationsfähigkeiten. Hands-on-Mentalität kann bei uns durch praktische Aufgaben in einer unserer drei Maschinenhallen mit modernster Infrastruktur ausgebaut werden.Getreu unserem Motto „PEM – Science for E-Mobility Production“, vereinen wir zehn Forschungsgruppen in vier Bereichen. Darin entwickeln wir die Produktionsprozesse von Elektrofahrzeugen und deren Komponenten (Batterie, Elektromotor und Brennstoffzelle) kontinuierlich weiter.Forschungsgruppe „Battery Engineering & Safety“ (BES)Die Forschungsgruppe „Battery Engineering & Safety“ am Lehrstuhl PEM leistet einen Beitrag zu leistungsfähigen, sicheren, nachhaltigen und wirtschaftlichen Batteriezellen und -systemen der Zukunft. Von der Durchführung strategischer Beratungsprojekte bis hin zur Untersuchung spezifischer, technischer Sachverhalte – sowohl konstruktiv und simulativ als auch operativ, mit Prototypen im Labor – widmet sich das Team nahezu allen Themen rund um das Produkt der Batteriezelle und des Batteriesystems. Das UmfeldUnsere vielseitigen und anspruchsvollen Themengebiete ermöglichen die enge Mitarbeit mit Führungs- und Fachkräften wegweisender OEMs, Automobilzulieferer, Maschinen- und Anlagenbauer sowie mit weiteren namhaften Industriepartnern. Die wissenschaftliche Tätigkeit gemeinsam mit anderen Forschungseinrichtungen erlaubt die Verfolgung eines eigenen Dissertationsthemas und die regelmäßige Veröffentlichung eigener Arbeitsergebnisse. Die Kombination aus methodischem Arbeiten mit dem Blick für das große Ganze und „technischen Tiefenbohrungen“ bietet unseren Mitarbeitenden ein einmaliges Umfeld zur persönlichen und fachlichen Weiterentwicklung. Ihr ProfilSie haben ein erfolgreich abgeschlossenes Hochschulstudium (Master oder vergleichbar) im technischen Bereich (bspw. Maschinenbau, Elektrotechnik, Wirtschaftsingenieurwesen).Sie haben idealerweise bereits erste praktische Erfahrung im Bereich Beratung, Entwicklung, Produktion oder E-Mobilität gesammelt.Sie haben den Selbstanspruch, neue Themen zu entwickeln und Gestaltungsspielraum zu nutzen.Sie arbeiten strukturiert und verbindlich, denken kreativ und pragmatisch, sind neugierig und motiviert, immer wieder Neues zu lernen.Sie verfügen über eine hohe Reisebereitschaft und sind flexibel.Sie sprechen und schreiben fließend Deutsch und Englisch.Ihre AufgabenSie gestalten Projekte mit Industriepartner/innen von der Akquise über die Planung bis hin zur Abwicklung entscheidend mit (bspw. in Produktions- und Prozessplanung, Prototyping und Strategieentwicklung im Bereich der Elektromobilität).Sie untersuchen im Rahmen von Forschungsprojekten spannende Fragestellungen zum Thema „Batterieentwicklung und -sicherheit“ sowie „innovative Batterietechnologien und Produktarchitekturen der Zukunft“.Sie entwickeln im Rahmen von Forschungs- und Industrieprojekten Prototypen und neue Überwachungs- sowie Testverfahren.Sie betreuen Studierende bei ihren Abschlussarbeiten und führen Lehrveranstaltungen durch.Sie erhalten frühzeitig Budget- und Führungsverantwortung und können eigenverantwortlich Themen gestalten.Wir bieten Ihnen30 Tage Urlaub bei Vollzeitanstellung inkl. Brückentage-RegelungFlexible Arbeitszeiten durch GleitzeitMöglichkeit der teilweisen Home-Office-ArbeitEvents für alle Mitarbeitenden sowie Team-EventsJahressonderzahlung, sofern die Anspruchsvoraussetzungen erfüllt sindModerne IT-AusstattungÜber unsDie RWTH ist als familiengerechte Hochschule zertifiziert.Die RWTH bietet im Rahmen eines Universitären Gesundheitsmanagements eine Vielzahl von Gesundheits-, Beratungs- und Präventionsangeboten (z. B. Hochschulsport) an. Für Tarifbeschäftigte und Beamtinnen und Beamte besteht ein umfangreiches Weiterbildungsangebot und die Möglichkeit, ein Jobticket zu erwerben.Die Stellenausschreibung richtet sich an alle Geschlechter.Wir wollen an der RWTH Aachen University besonders die Karrieren von Frauen fördern und freuen uns daher über Bewerberinnen.Frauen werden bei gleicher Eignung, Befähigung und fachlicher Leistung bevorzugt berücksichtigt, sofern sie in der Organisationseinheit unterrepräsentiert sind und sofern nicht in der Person eines Mitbewerbers liegende Gründe überwiegen.Bewerbungen geeigneter schwerbehinderter Menschen sind ausdrücklich erwünscht.Im Sinne der Gleichbehandlung bitten wir Sie, auf ein Bewerbungsfoto zu verzichten.Informationen zur Erhebung personenbezogener Daten nach Artikeln 13 und 14 Datenschutz-Grundverordnung (DS-GVO) finden Sie unter https://www.rwth-aachen.de/dsgvo-information-bewerbung.Besoldung / EntgeltEG 13 TV-L

Trainer Health and Safety (m/w/d) Meine Benefits: Zusammenarbeit in einem partnerschaftlichen Arbeitsumfeld Entwicklung deiner Fähigkeiten und Erweiterung deiner Kompetenzen Mitarbeit in einem internationalen Arbeitsumfeld Dienstfahrrad (Dein persönlich ausgesuchtes E-Bike für über 5.000,- €) Meine Aufgaben: Vorbereitung, Durchführung und Nachbereitung von theoretischen und praktischen Schulungen Erstellung von Präsentationen, Schulungsabläufen und Leitfäden Sicherstellung der Funktionssicherheit von Ausbildungsequipment sowie Überprüfung der Betriebsmittel Technischer Support der Trainer auf nationaler und internationler Ebene Umgang mit Gefahrstoffen Erstellung und Aktualisierung von Reparaturanweisungen und internen Regelungen Überwachung und Sicherstellung eigener Qualitätsvoraussetzungen Mein Profil: Abgeschlossenes Studium im Studiengang Chemie/Umwelttechnik oder technische Berufsausbildung im Bereich Gefahrstoffe/Gefahrgut als Chemikant, Umweltschutztechniker oder vergleichbar Berufserfahrung im Bereich Wissensvermittlung Sicherer Umgang mit MS Office und gute Englischkenntnisse Erfahrungen im Bereich Gefahrstoffe/Gefahrgut von Vorteil Ausgeprägte didaktische und rhetorische Fähigkeiten Teamfähigkeit und Belastbarkeit PKW Führerschein und Schwindelfreiheit Unser Auftraggeber: Großunternehmen Darauf kann ich mich bei DIEPA verlassen: Sozialversicherungspflichtige Beschäftigung im Rahmen der Arbeitnehmerüberlassung Unbefristetes Arbeitsverhältnis als Trainer Health and Safety Fahrrad-Leasing schon ab 14 EUR mtl. Individuelle Qualifikations- und Weiterbildungsmöglichkeiten Zugang zu unserem Benefit-Portal mit vielen Rabatten namhafter Partner Pünktliche und korrekte Lohnzahlung nach GVP-Tarif und den Branchenzuschlagstarifen Übertarifliche Zulagen Urlaubsgeld, Weihnachtsgeld, umfangreiches Prämienpaket Sehr gutes Arbeitsklima Persönliche Betreuung durch unsere Mitarbeiterinnen und Mitarbeiter Interessante Einsätze als Trainer Health and Safety bei namhaften Unternehmen in meiner Nähe Gute Chancen auf Übernahme durch unsere Kunden Diese Stelle passt nicht ganz zu Ihnen? Seit fast 30 Jahren sind wir als Personaldienstleister am Markt. Mit uns finden Sie Ihren neuen Job als Trainer Health and Safety ohne viel Papierkram. Wichtig sind uns Ihr Können und nicht Ihre Schulnoten. Jedes Jahr finden durch uns weit über 1.000 Menschen den Arbeitsplatz, der wie für sie gemacht ist. Vertrauen auch Sie auf Qualität und Wertschätzung in unserer Dienstleistung. Legen Sie los. Sie sind bereit für eine bessere Zukunft. Bewerben Sie sich jetzt. Eine Stellenanzeige von DIEPA GmbH