26 Jobs für Field Service Support in Mainz
Stellenangebote Field Service Support in Mainz Jobs
Job am 30.11.2025 bei StepStone gefunden
Vestas Wind Systems A/ S
• Mainz
Sabbaticals
[. .. ] us. With more than 185 GW of wind power installed worldwide and 40+ years of experience in wind energy, we have an unmatched track record demonstrating our [...]
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[...] expertise within the field. With 30, 000 employees globally, we are a diverse team united by a common goal: to power the solution today, tomorrow, and far into the future. As a Service Technician (m/f/d) , you, with your team will be responsible for the maintenance work on wind turbines (WTGs) , following standardized maintenance plans. Youll implement retrofits to enhance turbine efficiency, and document all tasks using modern digital tools. Alongside your technical responsibilities, your site presence greatly influences team [. .. ] yours, and well help you shape it. Our commitment to a fair hiring At Vestas, we evaluate all candidates solely based on their professional experience, education, and relevant skills. To support a fair recruitment process, we kindly ask that you remove any photos, dates of birth or graduation, gender pronouns, marital status, or other personal information not relevant to the role before submitting your CV/ resume. DEIB Statement At Vestas, we recognise the value of diversity, equity, and inclusion in driving [. .. ]
Job gestern bei Stellen-Online.de gefunden
Abb Vie Deutschland GmbH Co. KG
Compliance Manager Aesthetics DACH (all genders) - Vollzeit
• Mainz, 55116
At Allergan Aesthetics, an Abb Vie company, we develop, manufacture, and market a portfolio of leading brands and products in the
field of aesthetics. Our aesthetics portfolio includes facial injectables, [...]
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[...] body contouring, plastics, skin care, and more. Our goal is to consistently offer our customers innovation, education, exceptional service, and a commitment to excellenceall delivered with a personal touch. For more information, please visit Follow Allergan Aesthetics on Linked In. Allergan Aesthetics An Abb Vie company. Compliance Manager Aesthetics DACH (all genders) REF: R00137127 Job Description The Compliance Manager Aesthetics DACH (all genders) is responsible for coordinating and leading [. .. ] Europe and Canada. The role focuses on fostering a culture of compliance and upholding high ethical standards within the organization. Responsibilities Act as the OEC leader within the Affiliate and support the Affiliate General Manager and Area Compliance Director in key compliance activities. Lead and manage an effective Affiliate Compliance Insights Forum (ACIF) for D. A. C. H, engaging Affiliate Leadership Teams and Country Leaders as needed. Provide guidance, and support on complex ethics and compliance issues, including policy interpretation, compliance [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] to design, integrate, and implement ERP solutions that meet our business needs including budget management and adequate resource allocation. The jobholder owns the strategy of the IT [...]
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[...] unit to actively support Bio NTechs company goals, while ensuring compliance (SOX404, IT and Gx P) and scalability of all involved systems as well as process governance and cross-functional alignment of the functional teams. The head of ERP Applications Integration Solution Architecture is a critical role in ensuring that the cross functional and cross system [. .. ] a key contact in audits related with SAP ERP. Assure the IT, SOX404 and Gx P compliance of the SAP ERP-systems Develop and maintain strong relationships with external vendors and service providers that support the ERP systems, ensuring that they are meeting their contractual obligations and providing high-quality services Establish and maintain strong relationships with key stakeholders across the organization, including senior executives, other department heads, and business unit leaders What you have to offer: Completed relevant higher education and many years of professional experience in relevant field (10+ years) Deep understanding of integrated ERP systems and deep understanding in multiple SAP ERP modules. Experience in the pharmaceutical industry Experience in Gx P and SOX404 regulations Deep understanding of large-scale business transformations and ERP programs Experience in leading highly skilled people and/or leaders Strong communication and interpersonal [. .. ]
Job gestern bei Jobleads gefunden
Field Service Engineer (m/f/d) - Agilent Diagnostic Service in NRW
• Mainz, Rheinland- Pfalz
[. .. ] Deutschlandzentrale in Waldbronn bei Karlsruhe entwickeln, produzieren und vermarkten wir marktführende Analytik-Komplettlösungen. Einschließlich unserer Vertriebsbüros in München, Frankfurt, Hamburg und Ratingen sind über 1300 Mitarbeiter in Deutschland [...]
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[...] beschäftigt. Als Field Service Engineer (m/f/d) - Agilent Diagnostic Service in NRW ist es wichtig, hohe Bereitschaft zu haben sich kontinuierlich über neue Geräte, Software und Netzwerklösungen weiterzubilden. Kommunikationsfähigkeiten, Kreativität und eine positive Einstellung sind dabei von entscheidender Bedeutung. Durch die Fähigkeit, Kunden bei der Lösung ihrer Probleme zu unterstützen, und ein [. .. ] Verantwortlich für die Unterstützung von Kunden durch Vor-Ort-Aktivitäten wie Installation, Implementierung, Wartung und Reparatur von Medizingeräten in der Krebsdiagnostik, einschließlich Hardware, Software und Netzwerkprodukten sowie Betriebssystemen Einrichtung und Support von Software-/ Netzwerkprodukten um unsere Geräte bei Kunden am Einsatzort zu installieren Proaktive Reaktion auf mögliche Probleme mit Geräten oder Software, um zu verhindern, dass es bei unserem Kunden zu ungeplanten Verzögerungen in der Krebsdiagnostik kommt Ansprechpartner für technische Fragen und Produktunterstützung Zusammenarbeit mit Agilent-Teams wie Support, Vertrieb, Marketing [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
ADS
Field Service Engineer (m/f/d) in NRW Agilent inspiriert und unterstützt Entdeckungen, die zur Verbesserung der Lebensqualität beitragen. Wir versorgen Labore in den Bereichen Life Science, Diagnostik und angewandte Märkte [...]
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[...] weltweit mit Instrumenten, Dienstleistungen, Verbrauchsmaterialien, Anwendungen und Know-how. Agilent ermöglicht seinen Kunden, die Antworten und Erkenntnisse zu gewinnen, die sie [. .. ] Verantwortlich für die Unterstützung von Kunden durch Vor-Ort-Aktivitäten wie Installation, Implementierung, Wartung und Reparatur von Medizingeräten in der Krebsdiagnostik, einschließlich Hardware, Software und Netzwerkprodukten sowie Betriebssystemen Einrichtung und Support von Software-/ Netzwerkprodukten, um unsere Geräte bei Kunden am Einsatzort zu installieren Proaktive Reaktion auf mögliche Probleme mit Geräten oder Software, um zu verhindern, dass es bei unserem Kunden zu ungeplanten Verzögerungen in der Krebsdiagnostik kommt Ansprechpartner für technische Fragen und Produktunterstützung Zusammenarbeit mit Agilent-Teams wie Support, Vertrieb, Marketing [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Fachgebietsleiterin (w/m/d) Prüftechnik mit Fokus Luftreinhaltung und Lärmschutz
• Mainz, Rheinland- Pfalz
Homeoffice möglich Abgeschlossene Ausbildung
Firmenwagen Flexible Arbeitszeiten 30+ Urlaubstage Vermögenswirksame Leistungen
1 week ago Be among the first 25 applicants Industrial Services Cybersecurity At TÜV Rheinland, in the Industry
Service Cybersecurity business unit, we are looking for talents who are ready [...]
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[...] to help shape the future of the industry and accompany technological progress. Our focus is on digitalization and networking in the industry, as well as the further international expansion of our services in the field of renewable energy and support for major infrastructure projects. This applies to the functional safety of industrial plants in an era of rapidly increasing interconnectivity of components and machines the keyword being Operational Technology Security as well as to energy generation, utilization, and distribution, infrastructure, and network expansion. Our Core Areas Pressure Equipment Plant Engineering: [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
Jobticket
[. .. ] enhance efficiency and reduce costs Collaborate with global stakeholders to standardize processes and lead the integration of digital solutions and automation for improved data visibility, supplier collaboration, [...]
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[...] and operational performance Support the Global Process Owner S2P in defining the vision, strategy, and governance framework for the global S2P process, with specific responsibility for assigned sub-processes Lead governance meetings, collaborate on policy design, and serve as a key decision-maker to ensure alignment with global standards, priorities, and budgets Act as [. .. ] impactful reports and dashboards to communicate progress and insights to senior leadership What you have to offer: Completed Bachelors or Masters Degree in Business, Finance, Supply Chain or a related field, MBA or equivalent preferred 10+ years of experience ideally in procurement or related field within a large-scale, multinational environment, ideally in listed companies Previous experience in similar role is highly preferred, knowledgeable in direct and indirect procurement Proven ability to lead and influence in a matrixed, global environment, managing [. .. ] be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, Bio NTech will conduct the background check through our service provider Hire Right. You will be informed accordingly by your Bio NTech-Recruiter. #J-18808-Ljbffr 72361005 [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Associate Director Clinical Trials
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] program (s) . Ensure inspection readiness throughout the clinical program lifecycle. What You Have To Offer A Bachelors degree in the life sciences or a university degree [...]
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[...] in a related field with experience in the health industry (Advanced degree preferred) . Minimum 10 years of experience in the pharmaceutical/ biotech or related industry with at least 6 years experience in Global Clinical Development leading crossfunctional teams. Oncology experience required, registrational trial experience preferred. Knowledge and experience working with legislation and international [. .. ] proactively recognize risks and develop mitigations. PMP or equivalent certification desirable. Your Benefits Bio NTech is committed to the wellbeing of our team members and offers a variety of benefits in support of our diverse employee base. We offer competitive remuneration packages which are determined by the specific role, location of employment and also the selected candidates qualifications and experience. Note: The availability, eligibility and design of the listed benefits may vary depending on the location. The final requirements for the individual [. .. ] be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, Bio NTech will conduct the background check through our service provider Hire Right. You will be informed accordingly by your Bio NTech recruiter. We are looking forward to receiving your application. #J-18808-Ljbffr 72107602 [. .. ]
Job am 05.12.2025 bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] ensuring alignment with Bio NTechs business objectives and regulatory requirements. Drivelate-stage technical transferand Biologics License Application (BLA) readiness, ensuring seamless execution and compliance. Oversee Responses to Questions [...]
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[...] (RTQs) , launch support, GMP manufacturing investigations, process monitoring, and Annual Product Reviews (APRs) . Manage Post-Approval Change Management Plans (PACMP) to ensure product compliance and continuous improvement. Identify and mitigate product risks while driving technical improvements across the product lifecycle. Serve as amatrix product lead, providing guidance, training, and communication to MS [. .. ] continuous improvement. Monitor and analyze product performance, ensuring alignment with quality and regulatory expectations. Requirements Advanced degree (Masters or Ph. D. ) in Biotechnology, Biochemistry, Chemical Engineering, or a related field. Extensive experience inlate-stage product development, commercial manufacturing, andtechnical lifecycle management. Proven track record in CMC leadership, including technical transfer, regulatory submissions, and post-approval change management. Deep understanding of RNA and antibody-based products, control strategies, and regulatory compliance. Demonstrated ability to lead cross-functional teams and manage complex technical [. .. ] be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, Bio NTech will conduct the background check through our service provider Hire Right. You will be informed accordingly by your Bio NTech-Recruiter. Bio NTech, the story At Bio NTech, we are more than just a biotechnology company we are a community of innovators, scientists, and leaders dedicated to revolutionizing medicine by translating cuttingedge science into survival. Your contributions here have the potential [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
Manager Diagnostics Regulatory Affairs
• Mainz, Rheinland- Pfalz
[. .. ] affecting Bio NTechs drug developments and/or approvals Education and Professional Experience Relevant higher education (e. g. , Masters degree or Ph D) or extensive professional experience (typically [...]
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[...] 5years) in a related field Proven experience working in regulated, qualitycontrolled environments (e. g. , DIN EN ISO13485, GCP for laboratories) . Experience in support of internal and external audits and inspections by regulatory authorities (e. g. , FDA, Notified Bodies) and other thirdparties is a plus Skilled in preparing and assembling regulatory documents (e. g. , study submission packages for US FDA, EU IVDR) for medical devices or IVD medical devices, while integrating regulatory/ [. .. ] be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, Bio NTech will conduct the background check through our service provider Hire Right. You will be informed accordingly by your Bio NTech Recruiter. Bio NTech does not tolerate discrimination, favoritism or harassment based on gender, political views, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other physical or personal characteristics. [. .. ]
Job am 13.11.2025 bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
Jobticket
[. .. ] main responsibilities are: Contribute to the implementation and ongoing maintenance of the methodologies for Business Continuity, Emergency, and Crisis Management in collaboration with various stakeholders throughout its [...]
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[...] lifecycle Enable and support international locations in developing and maintaining Business Continuity Emergency Response Plans, including conducting Business Impact Analyses, as well as designing and implementing response strategies and measures Support the coordination and oversight of proactive measures and response strategies through simulations and exercises, assisting stakeholders and response teams in being well-prepared [. .. ] in business continuity, disaster recovery, or crisis management, preferably in the pharmaceutical, technology, or consultancy sectors Bachelors or Masters degree in Security Management, Business Administration, IT Security, or a related field Knowledge of relevant standards (e. g. , ISO 22301, BSI 200-4, ISO 22316, ISO 22361) is preferred Affinity for IT-controlled working methods and solutions Strong analytical skills, a structured and proactive approach to work, combined with effective communication abilities Willingness to travel occasionally, both national and internationally Strong [. .. ] be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, Bio NTech will conduct the background check through our service provider Hire Right. You will be informed accordingly by your Bio NTech Recruiter. #J-18808-Ljbffr 69374946 [. .. ]
Job am 06.11.2025 bei Jobleads gefunden
Director Scientific/ Medical Writing
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] required. The Director of Scientific/ Medical Writing has responsibilities as departmental subject matter expert for assigned role-relevant topics, e. g. , for specific processes such as for [...]
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[...] R D support, Medical Safety support, Biomarker support, etc. The Director of Scientific/ Medical Writing also has responsibilities as line manager, including for creating a cohesive, collaborative, innovative team which understands business needs, is highly flexible, and concentrates on delivering added value. This includes recruitment, supervision, and development of reports, as well as [. .. ] Pharm. D or a Ph. D. , ideally with background knowledge in immunology and oncology. Professional experience: 10 years (hands-on) experience working in drug development in a therapeutically relevant field, preferably in oncology and/or immunology. 10 years (hands-on) experience as a scientific or medical writer in the pharmaceutical/ biotech industry. Prior experience drafting documents for multiple indications, preferably in Bio NTech-relevant indications. Prior experience drafting alone new or updated CTPs and CSRs required for Phase I-III trials. [. .. ] be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, Bio NTech will conduct the background check through our service provider Hire Right. You will be informed accordingly by your Bio NTech Recruiter. We are looking forward receiving your application. Inspired? Become part of #Team Bio NTech. Bio NTech, the story At Bio NTech, we are more than just a biotechnology company we are a community of innovators, scientists, and leaders dedicated to [. .. ]
Job am 04.11.2025 bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
Jobticket
[. .. ] a crosslocation merger of several highly qualified genetic practices and laboratories. With a combination of medical values, quality and science, our common goal is to continue to [...]
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[...] dynamically advance the field of human genetics. Team play and fair, open interaction with one another are key elements for us. We have extensive experience in all areas of genetic diagnostics and are one of the leading genetic providers. In addition to our daytoday routine, we participate intensively in scientific studies and establish new, [. .. ] and counseling can only be offered in the long term with indepth processes and a basic medicalscientific attitude characterized by curiosity and empathy. Tasks Administration of the network infrastructure and support with client/ server administration Independent and projectbased work, as well as communication with external service providers Contributing to the conception of projects in the areas of IT infrastructure, IT security and data protection, their implementation and documentation Technical contact for IT support at the main site in Mainz (1st and 2nd level support for employees on site) Profile Relevant qualification, such as completed vocational training [. .. ]
Job am 02.11.2025 bei Jobleads gefunden
Director Protein ADC Analytics
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] to maintain state-of-the-art analytical methods for development in alignment with internal and external stakeholders Qualifications Masters degree or preferably Ph. D. in Analytical Chemistry or a related [...]
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[...] field, with at least 10 years of experience in an international, highly regulated environment Strong expertise in small molecule and ADC drug linkers analytical chemistry, including techniques such as HPLC, GC, mass spectrometry, NMR, and IR, with experience in assay development, validation, and statistical data analysis Proven experience in authoring CTD [. .. ] with excellent project management skills Strong communication and negotiation skills in English (German is a plus) , with the ability to convey complex technical matters concisely to diverse stakeholders We support you Your flexibility: flexible hours vacation account Your value: Your voice at the table Culture on an equal footing Opportunities to shape impact Support for your full potential Your health and lifestyle: Company bike Your life phases: Employer-funded pension Childcare Apply now-We look forward to your application Apply [. .. ] be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, Bio NTech will conduct the background check through our service provider Hire Right. You will be informed accordingly by your Bio NTech-Recruiter. Inspired? Become part of #Team Bio NTech. Bio NTech, the story At Bio NTech, we are more than just a biotechnology company we are a community of innovators, scientists, and leaders dedicated to revolutionizing medicine by translating cutting-edge science [. .. ]
Job am 02.11.2025 bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] company. Your main responsibilities: Ensure GTD-wide training alignment, maintain training profiles, and secure audit and inspection readiness Develop, implement, and oversee compliance frameworks, processes, and documentation within [...]
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[...] GTD to support Gx P requirements Safeguard data integrity and ensure digital compliance by aligning processes, data and systems within GTD to global digitalization initiatives Ensure adherence to quality systems, serve as key user for platforms (e. g. , Veeva e QMS) , and maintain ownership of guidance documents relevant to CMC development (e. g. [. .. ] and IT to maintain compliance across systems, monitor performance, identify gaps, and drive continuous improvement initiatives What you have to offer: Masters degree in pharmacy, Chemistry, Life Sciences, or related field with 5+ years in pharmaceutical development, process improvement, or compliance Deep understanding of global Gx P requirements and regulatory frameworks (FDA, EMA, ICH) Experience in designing and delivering compliance training programs Proficient in digital compliance tools, data integrity, and emerging pharma technologies Expertise in CMC documentation standards, audit readiness, and submission [. .. ] be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, Bio NTech will conduct the background check through our service provider Hire Right. You will be informed accordingly by your Bio NTech-Recruiter. Inspired? Become part of #Team Bio NTech. Bio NTech, the story At Bio NTech, we are more than just a biotechnology company we are a community of innovators, scientists, and leaders dedicated to revolutionizing medicine by translating cutting-edge science [. .. ]
Job am 02.11.2025 bei Jobleads gefunden
Director CMC Materials for Individualized Cancer Vaccines
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] Develop and implement strategies for the life cycle of raw materials and components required for production of individualized cancer vaccines, ensuring quality, regulatory compliance, supply chain robustness, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and scalability to support production for clinical trials and commercial production. Facilitate collaboration across key functions, including Quality, Supply Chain Management, Procurement, Regulatory Affairs, Manufacturing, Quality Control, Process Development, Analytics, and Project Management. Oversee the entire life cycle of raw materials and components, from clinical development through to commercialization, ensuring all materials meet regulatory [. .. ] associated with material supply, quality, and scalability. Drive continuous improvement initiatives to optimize material sourcing, reduce costs, ensuring readiness for commercial-scale production. Your profile. A degree in a scientific field; an advanced degree (e. g. , MSc, Ph D) is strongly preferred. At least 810 years of experience in the pharmaceutical or biotechnology industry, with a minimum of 5 years specializing in materials management. In-depth knowledge of GMP regulations and biopharmaceutical manufacturing requirements, particularly in relation to materials. Expertise in [. .. ] be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, Bio NTech will conduct the background check through our service provider Hire Right. You will be informed accordingly by your Bio NTech-Recruiter. Inspired? Become part of #Team Bio NTech. Bio NTech, the story At Bio NTech, we are more than just a biotechnology company we are a community of innovators, scientists, and leaders dedicated to revolutionizing medicine by translating cutting-edge science [. .. ]
Job am 28.10.2025 bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
At Tech Biz Global, we are providing recruitment
service to our TOP clients from our portfolio. We are currently seeking a SR. Regional Sales Manager to join one of [...]
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[...] our clients teams. If youre looking for an exciting opportunity to grow in a innovative environment, this could be the perfect fit for you. Responsibilities Direct Sales and Key Account [. .. ] maintain relationships with key customer stakeholders, including executives, technical teams, and procurement departments. Serve as the trusted advisor for customers by providing market insights, solution recommendations, and strategic guidance to support their business objectives. Organize and lead regular business and technical reviews with customers, ensuring alignment with their evolving needs and driving account growth. Strategic Market Development Develop and execute regional sales strategies aligned with company strategy and goals, focusing on the unique requirements of the network infrastructure, industrial IOT and [. .. ] new growth opportunities. Collaborate closely with internal product and marketing teams to position innovative solutions that address customer challenges and with industry trends. Internal Collaboration and Reporting Align closely with Field Application Engineers, Product Managers, and Technical Support to ensure customers receive comprehensive solutions and support. Deliver detailed and accurate sales forecasts, account plans, and progress reports to regional and executive leadership. Share insights from the field to inform product development, marketing strategies, and business planning. Deliverables Achieve or exceed assigned [. .. ]
Job am 23.10.2025 bei Jobleads gefunden
Product Owner Asset Management Omnichannel Engagement
• Mainz, Rheinland- Pfalz
Jobticket
[. .. ] in Mainz, Germany full time. Responsibilities Collaborate with stakeholders to collect requirements, design solutions, prioritize features, and ensure alignment with both business objectives and technical demands. Oversee [...]
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[...] contracts and manage service delivery processes. Guide, make decisions, approve, and manage the implementation of value-driven changes on platforms in collaboration with vendor teams. Establish and share the vision, objectives, and global roadmap for the digital capabilities under your responsibility, ensuring they align with the customer engagement platform strategy, business goals, and overall user experience. Facilitate organizational change management by delivering clear communication, providing tool training support, and maintaining comprehensive documentation. Track system performance, address issues, and work with technical teams to maintain high availability, security, and compliance with IT standards. Qualifications Completed studies in Business Informatics, Computer Science, or a related field. Several years of proven experience with Veeva systems as well as a strong understanding of digital asset management and omnichannel engagement strategies. Handson experience with global or U. S. based rollout projects. Ability to translate business needs into technical requirements, prioritize features, and align digital capabilities with broader organizational goals. [. .. ]
Job am 21.10.2025 bei Jobleads gefunden
• Mainz, Rheinland- Pfalz
Beratungs-/ Consultingtätigkeiten Homeoffice möglich
Sabbaticals
Service Technician (m/f/d) for Rotor Blade Maintenance on Wind Turbines at Vestas Deutschland Raum Karlsruhe-Heilbronn-Heidelberg, Germany About Vestas Vestas, a leader in sustainable energy solutions. We design, manufacture, install, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and maintain wind turbines in over 80 countries. In Germany, weve been active since 1986 and have installed [. .. ] and refurbish rotor blades using laminating resins and composite materials. Follow safety protocols and use protective equipment. Document maintenance activities with modern digital tools. Collaborate with the maintenance team to support site operations. Qualifications Skilled craftsmanship with a precise, detail-oriented approach. Technical understanding of epoxy resins, fiberglass, and carbon fiber materials. Detailed understanding of safety protocols, especially when handling hazardous substances. Ability to work without supervision and create technical documentation. Comfortable using Microsoft and i OS systems; SAP experience is a [. .. ] our Vestas Academy, youll receive structured, interactive training and can earn qualifications. As your skills grow, so do your opportunities, whether you aim to become a Lead Technician, take on Field Trainer responsibilities, or develop into a specialist role in major component exchanges or commissioning. Your future is yours, and well help you shape it. #J-18808-Ljbffr 66744175 [. .. ]
Job am 19.10.2025 bei Jobleads gefunden
Product Owner Core Engagement Platform
• Mainz, Rheinland- Pfalz
Jobticket
[. .. ] customer reference data flows. Partner with internal and external stakeholders to gather requirements, define solutions, prioritize features, and ensure both business and technical needs are met Oversee [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] contracts and manage service delivery processes Steer, decide, approve, manage and release value-driven changes on the platforms with our vendor teams Define and communicate the vision, goals, and global roadmap for the digital capabilities you are responsible for, ensuring alignment with the customer engagement platform strategy, business needs and overall user experience Support organizational change management by providing clear communication and create/ manage with our vendors tool training support, and documentation What you have to offer. Completed studies in Business Informatics, Computer Science, or a related field Proven experience with change projects including Integration Platform as a Service (IPaa S) systems, such as Mule Soft Handson experience with global or U. S. -based rollout projects for Master Data Management (MDM) systems Familiarity with Customer Identification and Access Management (CIAM) solutions, such as Salesforce Identity Experience with Reltio or [. .. ]
Job am 16.09.2025 bei Jobleads gefunden
Associate Director Scientific/ Medical Writing
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
[. .. ] largely according to standard procedures. Coordinate the document preparation, review, and approval. Check and revise documents with regard to scientific content, completeness, consistency, and standards compliance. Manage [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] outsourced tasks: Plan, support So W set up, coordinate, and manage external writers providing medical writing services. Foster knowledge (i. e. , by supporting, training, and guiding) and compliance with relevant processes, templates, and standards. Foster knowledge (i. e. , by supporting, training, and guiding) and compliance with good writing practices and the structure/ formatting [. .. ] M. D. or Pharm. D or a Ph. D. , ideally with background knowledge in immunology and oncology. 5 years (handson) experience working in drug development in a therapeutically relevant field, preferably in oncology and/or immunology. 5 years (handson) experience as a scientific or medical writer in the pharmaceutical/ biotech industry. Prior experience drafting documents for multiple indications, preferably in Bio NTechrelevant indications. Prior experience drafting alone new or updated CTPs and CSRs required for Phase IIII trials. Prior experience drafting low [. .. ] be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, Bio NTech will conduct the background check through our service provider Hire Right. You will be informed accordingly by your Bio NTech Recruiter. We are looking forward receiving your application. Inspired? Become part of #Team Bio NTech. Bio NTech, the story At Bio NTech, we are more than just a biotechnology company we are a community of innovators, scientists, and leaders dedicated to [. .. ]
Job am 09.09.2025 bei Jobleads gefunden
Construction Manager Mainz (m/f/d)
• Mainz, Rheinland- Pfalz
Homeoffice möglich
Sabbaticals Work-Life-Balance
[. .. ] our planned wind farms. Do you have experience in overseeing construction projects? Then youre exactly who were looking for Become part of our team and apply now [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] at Prokon We support you with various financial benefits, including the promotion of company pension schemes and disability insurance, capital-forming benefits, and performance-based bonus payments. Additionally, we offer discounted access to Prokon electricity, discounts through our corporate benefits platform, and affordable private use of company cars. Work-Life-Balance Predictable working hours, [. .. ] We place great importance on ensuring that you can balance your professional and private life as effectively as possible. Therefore, we also offer a holiday entitlement that increases with company service and significantly exceeds the statutory requirements, special leave days, and the option of unpaid leave or sabbaticals. You will support the team with your expertise during the development phase of the projects. You will manage the planning for the construction of the wind farms infrastructure in the areas of civil [. .. ] You have a degree in civil engineering or relevant experience in a comparable position. You have relevant experience as a site manager on location. You have solid knowledge in the field of soil mechanics and geotechnical engineering. You have good English skills, both spoken and written. You possess a Class B driving licence. Do you recognise yourself? Then do not hesitate and send us your application today Prokon not only wants to give the climate a chance, but also enable everyone [. .. ]
Job vor 4 Tagen bei Neuvoo.com gefunden
Abb Vie Deutschland GmbH Co. KG
Compliance Manager Aesthetics DACH (all genders)
• Mainz
At Allergan Aesthetics, an Abb Vie company, we develop, manufacture, and market a portfolio of leading brands and products in the
field of aesthetics. Our aesthetics portfolio includes facial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] injectables, body contouring, plastics, skin care, and more. Our goal is to consistently offer our customers innovation, education, exceptional service, and a commitment to excellence-all delivered with a personal touch. For more information, please visit https:/ / global. allerganaesthetics. com/. Follow Allergan Aesthetics on Linked In. Allergan Aesthetics An Abb Vie company. Compliance Manager Aesthetics DACH (all genders) REF: R00137127Job Description The Compliance Manager Aesthetics DACH (all genders) [. .. ] Europe and Canada. The role focuses on fostering a culture of compliance and upholding high ethical standards within the organization. Responsibilities Act as the OEC leader within the Affiliate and support the Affiliate General Manager and Area Compliance Director in key compliance activities. Lead and manage an effective Affiliate Compliance Insights Forum (ACIF) for D. A. C. H, engaging Affiliate Leadership Teams and Country Leaders as needed. Provide guidance, and support on complex ethics and compliance issues, including policy interpretation, compliance [. .. ]
Job vor 4 Tagen bei Neuvoo gefunden
Agilent
Field Service Engineer (m/f/d) - Agilent Diagnostic Service in NRW
• Mainz, Rhineland- Palatinate
[. .. ] Deutschlandzentrale in Waldbronn bei Karlsruhe entwickeln, produzieren und vermarkten wir marktführende Analytik-Komplettlösungen. Einschließlich unserer Vertriebsbüros in München, Frankfurt, Hamburg und Ratingen sind über 1300 Mitarbeiter in Deutschland [...]
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[...] beschäftigt. Als Field Service Engineer (m/f/d) - Agilent Diagnostic Service in NRW ist es wichtig, hohe Bereitschaft zu haben sich kontinuierlich über neue Geräte, Software und Netzwerklösungen weiterzubilden. Kommunikationsfähigkeiten, Kreativität und eine positive Einstellung sind dabei von entscheidender Bedeutung. Durch die Fähigkeit, Kunden bei der Lösung ihrer Probleme zu unterstützen, und ein [. .. ] Verantwortlich für die Unterstützung von Kunden durch Vor-Ort-Aktivitäten wie Installation, Implementierung, Wartung und Reparatur von Medizingeräten in der Krebsdiagnostik, einschließlich Hardware, Software und Netzwerkprodukten sowie Betriebssystemen Einrichtung und Support von Software-/ Netzwerkprodukten um unsere Geräte bei Kunden am Einsatzort zu installieren Proaktive Reaktion auf mögliche Probleme mit Geräten oder Software, um zu verhindern, dass es bei unserem Kunden zu ungeplanten Verzögerungen in der Krebsdiagnostik kommt Ansprechpartner für technische Fragen und Produktunterstützung Zusammenarbeit mit Agilent-Teams wie Support, Vertrieb, Marketing [. .. ]
Job vor 9 Tagen bei Neuvoo gefunden
usajobs. gov
Elektroingenieur (m/w/d) in Wiesbaden
• Mainz, Rhineland- Palatinate
Homeoffice möglich Abgeschlossenes Studium
30+ Urlaubstage Tarifvertrag Vermögenswirksame Leistungen
[. .. ] system and associated network infrastructure in the entire European theater. Employment: Full-time; permanent Duty Location: Wiesbaden, Germany. Salary: 4.746, 11-6.529, 04 monthly tied to length in
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[...] class=highlight_text>service Your Tasks: Developing of planning documents in accordance with German and American laws and regulations Planning and examining of electrical installation Processing of national and international projects in the
field of switchboards, lighting, installation systems, USV systems and generators. Calculation of low voltage networks Cost determination and offer processing Project development and quality control of planning documents from external offices Participation in project development, planning and construction meetings Duty Travel between. 10-15 of the entire work time Your Profile: [. .. ] for the position. The job advertisement and internal application form (profile) can be found on the following website: If you send your application directly via, we will contact you and
support you with your application process on our career page. If you only apply via and do not use our career page, your application cannot be considered. Become a part of the U. S. American security architecture for Europe. U. S. Army Europe and Africa is the cornerstone of peace and [. .. ]
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Wieviel verdient man als Field Service Support pro Jahr?
Als Field Service Support verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Field Service Support Jobs in Mainz bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 26 offene Stellenanzeigen für Field Service Support Jobs in Mainz.
Zu welchem Berufsfeld gehören Field Service Support Jobs in Mainz?
Field Service Support Jobs in Mainz gehören zum Berufsfeld Servicetechniker.
