Der GPR Gruppe zugehörig sind die Tochtergesellschaften GPR Medizinisches Versorgungszentrum gemeinnützige GmbH mit mehreren Standorten im Rhein-Main-Gebiet sowie die GPR Service GmbH. Das GPR Gesundheits- und Pflegezentrum Rüsselsheim gewährleistet mit diesem Zusammenschluss das Angebot einer umfangreichen medizinischen und pflegerischen Versorgung für die Bürgerinnen und Bürger der Stadt Rüsselsheim am Main und der Region.
Der GPR Gruppe zugehörig sind die Tochtergesellschaften GPR Medizinisches Versorgungszentrum gemeinnützige GmbH mit mehreren Standorten im Rhein-Main-Gebiet sowie die GPR Service GmbH. Das GPR Gesundheits- und Pflegezentrum Rüsselsheim gewährleistet mit diesem Zusammenschluss das Angebot einer umfangreichen medizinischen und pflegerischen Versorgung für die Bürgerinnen und Bürger der Stadt Rüsselsheim am Main und der Region.
Studienzentrum Dr. med Keller sucht in Frankfurt am Main eine/n Study Nurse / Studienassistenz (m/w/d) (ID-Nummer: 13313173)
Der GPR Gruppe zugehörig sind die Tochtergesellschaften GPR Medizinisches Versorgungszentrum gemeinnützige GmbH mit mehreren Standorten im Rhein-Main-Gebiet sowie die GPR Service GmbH. Das GPR Gesundheits- und Pflegezentrum Rüsselsheim gewährleistet mit diesem Zusammenschluss das Angebot einer umfangreichen medizinischen und pflegerischen Versorgung für die Bürgerinnen und Bürger der Stadt Rüsselsheim am Main und der Region.
Der GPR Gruppe zugehörig sind die Tochtergesellschaften GPR Medizinisches Versorgungszentrum gemeinnützige GmbH mit mehreren Standorten im Rhein-Main-Gebiet sowie die GPR Service GmbH. Das GPR Gesundheits- und Pflegezentrum Rüsselsheim gewährleistet mit diesem Zusammenschluss das Angebot einer umfangreichen medizinischen und pflegerischen Versorgung für die Bürgerinnen und Bürger der Stadt Rüsselsheim am Main und der Region.
Saphir Radiochirurgiezentrum Frankfurt am Main GmbH sucht in eine/n MFA (m/w/d) - Medizinische/r Fachangestellte/r (m/w/d) (ID-Nummer: 13668117)
Grant Thornton AG Wirtschaftsprüfungsgesellschaft sucht in Düsseldorf, Frankfurt am Main eine/n Werkstudent Audit - Professional Practice Group (m/w/d) (ID-Nummer: 13685882)
Auf einen Blick Ausgeschrieben seit: 13.03.2026 Branche: Lager / Logistik Tätigkeitsbereich: Leiter/in - Logistik Einsatzort: Frankfurt am Main Bewerbung: Ohne Anschreiben Referenz-Nr.: 104242A48026
Auf einen Blick Ausgeschrieben seit: 13.03.2026 Branche: Lager / Logistik Tätigkeitsbereich: Leiter/in - Logistik Einsatzort: Frankfurt am Main Bewerbung: Ohne Anschreiben Referenz-Nr.: 104242A48026
The IT JDA Specialist is accountable for the Implementation of IT solutions (JDA) that meet the needs of the business and our clients within the budgets and times defined by the projects. Main Accountabilities: Implement the tasks required to meet the requirements of operations / customers on the IT solution under their area of responsibility.Document, record and maintain all the technical knowledge necessary to respond to IT needs on the IT Solution under its area of responsibilityApply the operational execution of IT services, ensuring the application of good practices (eg ITIL) and aligned with the DP DHL guidelines (registration and management documentation).Detection, control and verification of IT security systems, applying the DP-DHL guidelines as well as state legal frameworks (license management, access security, LOPD, etc ...).
Auf einen Blick Ausgeschrieben seit: 10.03.2026 Branche: Produktion Tätigkeitsbereich: Produktionsleiter (m/w/d) Einsatzort: Frankfurt am Main Bewerbung: Ohne Anschreiben Referenz-Nr.: 105558A48040
Auf einen Blick Ausgeschrieben seit: 10.03.2026 Branche: Produktion Tätigkeitsbereich: Produktionsleiter (m/w/d) Einsatzort: Frankfurt am Main Bewerbung: Ohne Anschreiben Referenz-Nr.: 105558A48040
Stellenbeschreibung Die DEKRA Arbeit GmbH sucht für eine Finanzbehörde eine/n erfahrene/n Projekt Koordinator (m/w/d) in Frankfurt am Main. In dieser verantwortungsvollen Position stellen Sie die Koordination komplexer, organisationsübergreifender Projekte sicher, fungieren als Schnittstelle zwischen technischen und fachlichen Bereichen und gewährleisten die Einhaltung von Governance-, Compliance- und Projektvorgaben.
Wir bringen Leistung. Zusammen. Arbeitsort: Frankfurt am Main Job-ID: 11618 BPS24! 40 Wochenstunden Die BPS Personalmanagement GmbH ist eine moderne Personalberatungs- und Coachingagentur. Im Auftrag eines Kundenunternehmens in Frankfurt am Main ist die Stelle Senior Produktmanager Payment & Go-to-Market (m/w/d) zum nächstmöglichen Zeitpunkt zu besetzen.
Mit mehr als 3000 zufriedenen und motivierten Mitarbeitern und einem jährlichen Umsatz von über einer Milliarde Euro ist dieses namhafte Unternehmen stetig am wachsen. Zur Verstärkung des Teams in Frankfurt am Main, suchen wir zum 01.04.2026 einen erfahrenen HR Business Partner (m/w/d) als befristete Elternzeitvertretung, der Führungskräfte und Mitarbeitende im operativen Tagesgeschäft begleitet und als verlässlicher Ansprechpartner für alle personalrelevanten Themen im DACH-Raum agiert.
In your position, you also contribute to setting standards and best practices for your team and support exploring new methodologies and practices. Main tasks Independently manage process optimization and redesign projects according to established project management and standardization methodologies (e.g.
Your task Be part of a global team acting as a think tank for the organization to develop and incubate innovation and improvement projects. Your main role is to support work-streams for a global strategic project enhancing data visualization for top management as well as supporting workstreams of other mid to complex projects that contribute to Operations performance.
Your role The Sales Engineer is a high-impact, customer-facing role that serves as the main link between the Leybold factory and the client. Responsible for driving sales, this role educates key stakeholders on vacuum technology advancements and best practices.
Jones Lang LaSalle SE Human Resources Dein Ansprechpartner: Gerphill Ballecer Gerphill.Ballecer@jll.com https://www.linkedin.com/in/gerphillballecer/ #LI-GB3 Location: On-site –Berlin, DEU, Düsseldorf, DEU, Frankfurt am Main, DEU, Hamburg, DEU, Hannover, DEU, Köln, DEU, Munich, DEU If this job description resonates with you, we encourage you to apply even if you don’t meet all of the requirements.
Jones Lang LaSalle SE Your contact: Marta Marunchak marta.marunchak@jll.com #LI-MM4 Location: On-site –Frankfurt am Main, DEU If this job description resonates with you, we encourage you to apply even if you don’t meet all of the requirements. We’re interested in getting to know you and what you bring to the table!
Furthermore, you will need to gain an oversight to assure achievement of trial recruitment commitment, timelines, budget and quality standards. MAIN RESPONSIBILITIES • Manage the execution of clinical studies or assigned portion of Early Phase clinical studies; including orchestration of local trial team, and integration with other functions as necessary throughout planning, conduct and closeout of trial. • Work within a complex GCP and regulatory environment and on global clinical trials with multidisciplinary, international teams and with various internal and external stakeholders including suppliers and investigational sites. • Lead and support local trial team and investigative sites in timely preparation of required trial documents, contracts, and necessary approvals. • Ensure compliance with ICH-GCP and all other relevant regulatory regulations as well as accordance with client SOPs and values. • Assure highest ethical and professional standards, patient safety, and that local component of trial is planned, conducted, and reported in line with regulatory requirements. • Set up, manage, and review operating unit trial budget to ensure appropriate level of financial oversight and timely budget updates based on trial changes. • Assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements. • Ensure appropriate trial-specific training of internal and external partners in line with Trial Training Plan. • Develop and maintain relationships with investigational sites and support CRAs in site contacts. • In collaboration with Site Monitoring Lead and CRAs, ensure: o provision of appropriate trial oversight for the trials by monitoring compliance of trial sites and team to GCP, local regulations, customer SOPs, and adherence to trial protocol. o adequate trial supply distribution to sites. o continuous and timely data entry and cleaning, and on time Data Base Lock. o collection of required documents, with timely, complete, and compliant archiving of all relevant documents for the eTMF and CTR Appendices. • Identify risks and contingencies and partner with project leader in problem solving and resolution efforts. • Report to and relate with Trial Leader to provide updates, exchange critical information and share trial conduction information, within regulatory and compliance burdens. • Participate in and actively drive organizational, quality and process improvement initiatives to commence future leading change.
You will have two direct reports (chemists/technologists) and report to the Chief Production Officer (CPO) based in Vojens, Denmark. Your main responsibilities will include: Own the chemistry of our solid propellants – develop, document, and validate all fuel formulations and recipe control standards Define and maintain critical process parameters (temperature, mixing time, vacuum, catalysts, etc.) and ensure robust process windows from lab scale to full-scale production Lead and manage the analytical laboratory: raw material testing, in-process testing, test methodologies, calibration, documentation, and data traceability Drive recipe change control – plan and execute pilot batches, validation, and transfer to production, including updates of SOPs and work instructions Conduct root-cause analysis in collaboration with Process Engineering and Maintenance to address recurring defects, quality deviations and process instability Ensure full batch traceability and strong HSE practices for hazardous materials (classification, storage, transport, and safe handling) Collaborate closely with Quality Control to define sampling plans, acceptance criteria and CAPA activities (Corrective and Preventive Actions) Contribute to supplier qualification and material approval, including definition and verification of technical specifications Continuously improve yield, scrap rate and recipe cost through optimization of formulations and process parameters Maintain and prepare documentation for ISO, AQAP and defense-quality audits related to chemical operations Lead, coach, and develop your team of chemists and technologists and help build a strong safety- and quality-driven culture on site We are looking for an experienced and hands-on chemical leader who thrives in a high-tech, safety-critical production environment and enjoys building something new.
This position provides opportunities for promotions after gaining certain experience and a proven record of accomplishment. Main tasks Support process optimization and redesign projects according to established project management and standardization methodologies (e.g.
You will have two direct reports (chemists/technologists) and report to the Chief Production Officer (CPO) based in Vojens, Denmark. Your main responsibilities will include: Own the chemistry of our solid propellants – develop, document, and validate all fuel formulations and recipe control standardsDefine and maintain critical process parameters (temperature, mixing time, vacuum, catalysts, etc.) and ensure robust process windows from lab scale to full-scale productionLead and manage the analytical laboratory: raw material testing, in-process testing, test methodologies, calibration, documentation, and data traceabilityDrive recipe change control – plan and execute pilot batches, validation, and transfer to production, including updates of SOPs and work instructionsConduct root-cause analysis in collaboration with Process Engineering and Maintenance to address recurring defects, quality deviations and process instabilityEnsure full batch traceability and strong HSE practices for hazardous materials (classification, storage, transport, and safe handling)Collaborate closely with Quality Control to define sampling plans, acceptance criteria and CAPA activities (Corrective and Preventive Actions)Contribute to supplier qualification and material approval, including definition and verification of technical specificationsContinuously improve yield, scrap rate and recipe cost through optimization of formulations and process parametersMaintain and prepare documentation for ISO, AQAP and defense-quality audits related to chemical operationsLead, coach, and develop your team of chemists and technologists and help build a strong safety- and quality-driven culture on site We are looking for an experienced and hands-on chemical leader who thrives in a high-tech, safety-critical production environment and enjoys building something new.