124 Jobs für Regulatory Coordinator
Stellenangebote Regulatory Coordinator Jobs
Neu Job vor 6 Std. bei StepStone gefunden
Trelleborg Antivibration Solutions Germany GmbH
• Velten, Laudenbach Laudenbach;Landkreis Miltenberg
[. .. ] key industries and critical infrastructure. We are one of three business areas within the Trelleborg Group and employ approximately 6, 200 people worldwide. About the job As [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Customer Service Coordinator (m/f/d) you will be responsible for managing customer orders and communications, ensuring timely confirmations and proactive engagement. This involves coordinating forecasts, delivery, and planning with internal teams, maintaining customer portals and safety stock, and supporting financial processes such as credit/ debit notes and receivables. You will handle complaints, ensures regulatory compliance (e. g. export control) for deliveries, and manages special transport registrations Kindly take note that this is a 2 year fixed term contract position. Create and send order confirmations to customers, ensuring accuracy and timeliness. Build strong operational relationships by proactively informing and engaging with customers. Gather customer forecasts [. .. ]
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Job vor 3 Tagen bei Jooble gefunden
Hays Professional Solutions GmbH
Label Change Coordinator (m/w/d)
• Heppenheim
Angebote von Zeitarbeitsunternehmen
[. .. ] qualitativ einwandfreie Umsetzung zu gewährleisten Sie kommunizieren mit internen Grafikern, Lohnherstellern sowie externen Vertriebspartnern und sorgen für einen reibungslosen Informationsfluss sowie effiziente Abstimmungsprozesse Zudem fungieren Sie als [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Schnittstelle zwischen Pharmakovigilanz, Regulatory Affairs, Quality und Supply Chain und stellen sicher, dass alle relevanten Anforderungen in den Labeling-Prozessen berücksichtigt werden Ihre Qualifikationen: Sie bringen ein abgeschlossenes naturwissenschaftliches oder pharmazeutisches Studium (z. ? B. Pharmazie, Biologie, Chemie, Medizinprodukte-Technologie) oder eine vergleichbare Qualifikation im Gesundheitsbereich mit Sie besitzen Erfahrung im Labeling von Arzneimitteln oder [. .. ]
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Job vor 6 Tagen bei Jooble gefunden
Hologic
• Berlin
[. .. ] manage customer requests, troubleshoot order processing issues, coordinate exciting projects, like our Mammography Trailer Business, and ensure a seamless customer journey from lead to close. You will [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] be the central coordinator within the commercial ecosystem, bridging customer needs with internal operational excellence. The role supports the sales team and it is mainly office based, cross-functional collaboration is essential. If you thrive in a fast-paced environment, love solving problems, and are passionate about helping customers, this is the perfect opportunity [. .. ] projects, focusing on timelines, resources, budgets, and status reports Optimize order-to-delivery processes for the trailer business, ensuring accuracy and compliance Collaborate cross-functionally to facilitate installations, billing, and regulatory compliance Create and manage purchase orders for new customers and contractors Communicate clearly with customers about training, installations, and project updates Accurately record project and installation data, and distribute necessary documentation for invoicing Proactively identify and solve blockers in the sales order process What You Bring: Commercial or technical education [. .. ]
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Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Contract Clinical Research Associate
• Wiesbaden
Work-Life-Balance
[. .. ] local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, and Abb Vie Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site personnel on the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] protocol and applicable regulatory requirements in collaboration with pertinent project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the [. .. ] equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
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Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, and Abb Vie Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site personnel on the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] protocol and applicable regulatory requirements in collaboration with pertinent project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the [. .. ] equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
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Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Study Specialist (Contract)
• Wiesbaden
Work-Life-Balance
[. .. ] local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, and Abb Vie Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site personnel on the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] protocol and applicable regulatory requirements in collaboration with pertinent project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the [. .. ] equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
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Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, and Abb Vie Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site personnel on the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] protocol and applicable regulatory requirements in collaboration with pertinent project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the [. .. ] equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
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Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Senior Research Associate
• Wiesbaden
Work-Life-Balance
[. .. ] local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, and Abb Vie Standard Operating Procedures (SOPs) and business processes, if applicable. Trains study site personnel on the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] protocol and applicable regulatory requirements in collaboration with pertinent project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the [. .. ] equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
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Job vor 8 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] business processes, if applicable. Manages the activities of clinical investigative sites across multiple protocols and multiple therapeutic areas, with appropriate supervision Trains study site personnel on the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] protocol and applicable regulatory requirements in collaboration with pertinent project team members. Appropriately escalates serious or outstanding issues. Facilitates Quality Assurance Audit processes as indicated. Ensures regulatory inspection readiness at assigned clinical sites. Reports monitoring activities and study site conduct accurately and completely. Prepare and submit written reports, both monitoring and administrative, with appropriate [. .. ] Current knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials is preferred Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Knowledge related to ICH/ GCP Guidelines and applicable local regulations is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, [. .. ]
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Job vor 14 Tagen bei Jooble gefunden
Thermo Fisher Scientific
Clinical Trial Coordinator II (m/f/d) - Germany
• Karlsruhe
[. .. ] dedicated, forward-thinking and upbeat teams. A day in the Life: Performs PPD clinical research services investigator file reviews and logging of outstanding issues in project related tracking [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] tools Reviews regulatory documents for proper content Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD clinical research services departments Assists with the identification of potential investigators and development/ distribution of initial protocol packets [. .. ]
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Job am 24.01.2026 bei Jooble gefunden
Midas Pharma GmbH
• Ingelheim am Rhein
30+ Urlaubstage
[. .. ] und Kooperationspartnern und damit einhergehende Reisetätigkeit (national und international) Koordination und Kooperation von und mit internen, in die Supply Chains involvierten Fachabteilungen, wie z. B. : Quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Management, Business Development, Regulatory Affairs, Finished Product Development, Legal Affairs, Finance Controlling und IP-Management Mindestens 5 Jahre relevante Berufserfahrung im Supply Chain Management der pharmazeutischen Industrie Nachweisbare Erfahrungen im Management von pharmazeutischen Fertigproduktpipelines, Kenntnisse in fertigproduktrelevanten pharmaspezifischen Themen, wie Qualität, Reg. Affairs oder Produktentwicklung sind von Vorteil Sehr gute Anwenderkenntnisse in ERP Systemen, [. .. ]
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Job am 16.01.2026 bei Jooble gefunden
Milestone One
Regional Clinical Operations Manager
• München
[. .. ] our regional activities and supporting the scalable, high-quality delivery of clinical research projects worldwide. The Operations Manager will take full operational ownership of assigned regions, leading site [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] operations, managing coordinator teams, and ensuring that clinical trials are executed efficiently, compliantly, and without disruption. This role requires a hands-on leader with deep knowledge of clinical trial operations who can proactively identify and resolve day-to-day challenges in a dynamic international environment. This is a regional role, with the region [. .. ] Responsibilities Take end-to-end operational responsibility for clinical research projects within the assigned region. Ensure effective execution of clinical trials in line with study protocols, timelines, quality standards, and regulatory requirements. Oversee site qualification process and ensure smooth study start-up, including site contracting support, site activation, and coordination with internal and external stakeholders. Lead, manage, and support regional teams of operational and BD staff. Act as a mentor and escalation point for coordinators facing operational challenges. Proactively manage risks, [. .. ]
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Job am 16.01.2026 bei Jooble gefunden
Milestone One
• München
[. .. ] our regional activities and supporting the scalable, high-quality delivery of clinical research projects worldwide. The Operations Manager will take full operational ownership of assigned regions, leading site [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] operations, managing coordinator teams, and ensuring that clinical trials are executed efficiently, compliantly, and without disruption. This role requires a hands-on leader with deep knowledge of clinical trial operations who can proactively identify and resolve day-to-day challenges in a dynamic international environment. Take end-to-end operational responsibility for clinical research projects within the assigned region. Ensure effective execution of clinical trials in line with study protocols, timelines, quality standards, and regulatory requirements. Lead, manage, and support regional teams of operational and BD staff. Proactively manage risks, troubleshoot operational bottlenecks, and lead local resolution Collaborate closely with internal global teams to ensure alignment, clear communication, and seamless project execution. Minimum 5 years of experience in leadingclinical trial operations within an SMO or CRO [. .. ]
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Job am 15.01.2026 bei Jooble gefunden
Infosys Consulting- Europe
Office Facilities Coordinator
• Garching, Garching an der Alz
Location: Garching Work Arrangement: 5 days/ week onsite Department: BEf/Office Facilities Role Purpose The Office Facilities
Coordinator ensures the efficient operation of the Garching office by managing day-to-day facilities [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities, supporting employee lifecycle processes, and providing administrative assistance to internal stakeholders. This role acts as a key point of contact for employees, visitors, and vendors, ensuring a well-organized, safe, and compliant work environment. Key [. .. ] absences. Offer general ad hoc administrative support to BEF and other internal stakeholders as needed. Support tasks related to the employee leasing licence, including maintaining accurate documentation and compliance with regulatory requirements. Requirements Full-time onsite presence (5 days/ week) in the Garching office. Strong organisational skills with high attention to detail and the ability to manage multiple tasks simultaneously. Excellent communication and interpersonal skills. Reliability, discretion, and a proactive, service-oriented attitude. Previous experience in office management, facilities coordination, or [. .. ]
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Job am 14.01.2026 bei Jooble gefunden
KBR, Inc.
• Vogtei
[. .. ] quality environments for service members, civilians, and their families. With a dedicated team operating from Houston, Texas and Stuttgart, Germany, the program is recognized for its adherence [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to industry standards, regulatory compliance, and continuous improvement, supporting mission-critical objectives for major commands such as EUCOM and AFRICOM. The programs achievements include timely facility maintenance, innovative service delivery, and a strong reputation for excellence within the Department of Defense community. Job Summary The GFEBS PM Coordinator Lead is responsible for the successful utilization and management of the General Fund Enterprise Business System (GFEBS) for preventive maintenance operations on a military installation. This role ensures accurate data entry, reporting, and coordination of maintenance activities, serving as the technical expert for GFEBS processes. The Coordinator Lead works closely [. .. ]
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Job am 14.01.2026 bei Jooble gefunden
Givaudan SA
Sales Project Coordinator (m/w/d)
• Hamburg
Betriebliche Altersvorsorge Weihnachtsgeld
[. .. ] Entschlossenheit prägen tagtäglich unsere Zukunft und beeinflussen Milliarden von Menschen positiv. Jeder Teil von dir ist eine Bereicherung für unsere Welt. Wir sind Givaudan. Human by nature. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Als Sales Project Coordinator (m/w/d) koordinierst du die vertrieblichen Abläufe im Innendienst und bist für diese dann auch verantwortlich. Du. . . verwaltest und eröffnest Projekte (Korrespondenz mit Kunden und Geschäftspartnern wie Vertretern/ Vertriebspartnern durch Organisation und Eingabe von Projektdetails in die relevanten Systeme von Givaudan) , um die Entwicklungsarbeit zu starten/ [. .. ] usw. arbeitest Angebote für unsere Kunden aus verwaltest die Kundenpreislisten bereitest Duftbeschreibungen und kleine Präsentationen vor und gibst diese an den Kunden weiter arbeitest eng mit den Abteilungen Customer Care, Regulatory Affairs, Commercial Lab, Developmen, Marketing und Pricing zusammen übernimmst die direkte Korrespondenz und Kommunikation mit Kunden schulst neue Teammitglieder in den relevanten Systemen erstellst Statistiken und Berichte Was wir uns von dir wünschen. . . eine abgeschlossene kaufmännische Ausbildung mind. 2 Jahre Berufserfahrung in einer ähnlichen Position idealerweise in der [. .. ]
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Job am 14.01.2026 bei Jooble gefunden
KBR, Inc.
• Vogtei
[. .. ] quality environments for service members, civilians, and their families. With a dedicated team operating from Houston, Texas and Stuttgart, Germany, the program is recognized for its adherence [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to industry standards, regulatory compliance, and continuous improvement, supporting mission-critical objectives for major commands such as EUCOM and AFRICOM. The programs achievements include timely facility maintenance, innovative service delivery, and a strong reputation for excellence within the Department of Defense community. Job Summary The GFEBS PM Coordinator Lead is responsible for the successful utilization and management of the General Fund Enterprise Business System (GFEBS) for preventive maintenance operations on a military installation. This role ensures accurate data entry, reporting, and coordination of maintenance activities, serving as the technical expert for GFEBS processes. The Coordinator Lead works closely [. .. ]
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Job am 14.01.2026 bei Jooble gefunden
Tec Alliance
Support Services Coordinator
• Köln
[. .. ] between IT, end users, and external service providers. Monitoring and reporting on service KPIs. Providing training and support to internal stakeholders. Coordinating service improvement initiatives. Ensuring compliance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with security and regulatory requirements in service operations. Requirements: Degree in Computer Science, Business Informatics, or equivalent qualification. Several years of experience in IT Service Management, ideally with Freshservice or similar platforms. ITIL Foundation certification (minimum) , ideally advanced ITIL certifications. Experience in process design and optimization. Strong communication skills and service-oriented mindset. [. .. ]
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Job am 14.01.2026 bei Jooble gefunden
Westinghouse Electric Company, LLC
• Mannheim
[. .. ] aspects of project execution: scope, schedule, cost, risk, procurement, quality, resources, and stakeholder engagement. Develop and maintain project management plans, baselines, and risk registers. Ensure compliance with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] safety, environmental, and regulatory requirements. Bachelors degree in Project Management, Engineering, Business, or related field. Experience: 5-10 years of project management experience in technical industries; proven track record managing large, complex projects (25M-120M) . Fluent English and German required; Spanish, French, or Italian is a plus. Advanced knowledge of scheduling and cost [. .. ]
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Job am 14.01.2026 bei Jooble gefunden
KBR, Inc.
Maintenance Project Manager (m/w/d)
• Vogtei
[. .. ] quality environments for service members, civilians, and their families. With a dedicated team operating from Houston, Texas and Stuttgart, Germany, the program is recognized for its adherence [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to industry standards, regulatory compliance, and continuous improvement, supporting mission-critical objectives for major commands such as EUCOM and AFRICOM. The programs achievements include timely facility maintenance, innovative service delivery, and a strong reputation for excellence within the Department of Defense community. Job Summary The GFEBS PM Coordinator Lead is responsible for the successful utilization and management of the General Fund Enterprise Business System (GFEBS) for preventive maintenance operations on a military installation. This role ensures accurate data entry, reporting, and coordination of maintenance activities, serving as the technical expert for GFEBS processes. The Coordinator Lead works closely [. .. ]
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Job am 14.01.2026 bei Jooble gefunden
KBR, Inc.
Project Manager Maintenance (m/w/d)
• Vogtei
[. .. ] quality environments for service members, civilians, and their families. With a dedicated team operating from Houston, Texas and Stuttgart, Germany, the program is recognized for its adherence [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to industry standards, regulatory compliance, and continuous improvement, supporting mission-critical objectives for major commands such as EUCOM and AFRICOM. The programs achievements include timely facility maintenance, innovative service delivery, and a strong reputation for excellence within the Department of Defense community. Job Summary The GFEBS PM Coordinator Lead is responsible for the successful utilization and management of the General Fund Enterprise Business System (GFEBS) for preventive maintenance operations on a military installation. This role ensures accurate data entry, reporting, and coordination of maintenance activities, serving as the technical expert for GFEBS processes. The Coordinator Lead works closely [. .. ]
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Job am 14.01.2026 bei Jooble gefunden
KBR, Inc.
GFEBS Project Manager
• Vogtei
Führungs-/ Leitungspositionen
[. .. ] quality environments for service members, civilians, and their families. With a dedicated team operating from Houston, Texas and Stuttgart, Germany, the program is recognized for its adherence [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to industry standards, regulatory compliance, and continuous improvement, supporting mission-critical objectives for major commands such as EUCOM and AFRICOM. The program s achievements include timely facility maintenance, innovative service delivery, and a strong reputation for excellence within the Department of Defense community. Job Summary The GFEBS PM Coordinator Lead is responsible for the successful utilization and management of the General Fund Enterprise Business System (GFEBS) for preventive maintenance operations on a military installation. This role ensures accurate data entry, reporting, and coordination of maintenance activities, serving as the technical expert for GFEBS processes. The Coordinator Lead works closely [. .. ]
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Job am 14.01.2026 bei Jooble gefunden
Hapeko
Supply Chain Coordinator (m/w/d) in der Pharmaindustrie (Supply-Chain-Manager/in)
• Kleinmachnow
Abgeschlossenes Studium
[. .. ] der Möglichkeit, aktiv am Unternehmensaufbau mitzuwirken. Koordination und Steuerung der gesamten Importprozesse für medizinisches Cannabis Sicherstellung der regulatorischen Compliance im Bereich Betäubungsmittel Enge Zusammenarbeit mit internen Teams [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (Supply Chain, Qualität, Regulatory Affairs) Abgeschlossenes Studium mit Schwerpunkt Supply Chain, Logistik oder vergleichbare Fachrichtung Mindestens 2 Jahre Berufserfahrung im Bereich Import/ Export, Logistik oder Supply Chain Sehr gute Kommunikationsfähigkeiten in Deutsch und Englisch (mindestens C1) Moderne Arbeitsausstattung und digitale Tools Kollegiales Team und offene Unternehmenskultur Vielfältige Entwicklungsmöglichkeiten zur Leitung SCM 75130683 [. .. ]
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Job am 20.01.2026 bei Jooble gefunden
INM- Leibniz- Institut für Neue Materialien gGmbH
Project Manager (m/w/d) Regulatory Affairs
• Saarland
Work-Life-Balance
[. .. ] science and synthetic biology, with huge potential for sustainable innovation in different technological and medical fields. Our institute develops safe-by-design concepts for responsible ELM innovation. Project Manager [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in Regulatory Affairs related to biotechnology/ biomedical products (f, m, d) The project manager will coordinate a knowledge-exchange network that links multiple stakeholders (academic institutions, industry, consultants and regulatory agencies) and experts with interest in ELM research, innovation and regulation. This project is framed within the collaborative network Material Vital Hub, [. .. ] development. Conceptualization of the outreach action plan (website, online platform, workshops) in cooperation with scientists in Material Vital Hub and communication experts at INM and partner institutions. Reporting to project coordinator, partners and funding agencies. Masters degree in Regulatory Affairs and at least 2 years of related work experience. Alternatively, university degree in natural, engineering or life sciences and several years experience in regulatory science or regulatory affairs. A Ph D in biomedical materials, microbiology, or experience in clinical translation of cell [. .. ]
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Job am 20.01.2026 bei Jooble gefunden
KBR
GFEBS Project Manager
• Moringen
Führungs-/ Leitungspositionen
[. .. ] quality environments for service members, civilians, and their families. With a dedicated team operating from Houston, Texas and Stuttgart, Germany, the program is recognized for its adherence [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to industry standards, regulatory compliance, and continuous improvement, supporting mission-critical objectives for major commands such as EUCOM and AFRICOM. The program s achievements include timely facility maintenance, innovative service delivery, and a strong reputation for excellence within the Department of Defense community. Job Summary The GFEBS PM Coordinator Lead is responsible for the successful utilization and management of the General Fund Enterprise Business System (GFEBS) for preventive maintenance operations on a military installation. This role ensures accurate data entry, reporting, and coordination of maintenance activities, serving as the technical expert for GFEBS processes. The Coordinator Lead works closely [. .. ]
▶ Zur Stellenanzeige

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Häufig gestellte Fragen
Wieviel verdient man als Regulatory Coordinator pro Jahr?
Als Regulatory Coordinator verdient man zwischen EUR 45.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Regulatory Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 124 offene Stellenanzeigen für Regulatory Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Regulatory Coordinator Jobs?
Aktuell suchen 49 Unternehmen nach Bewerbern für Regulatory Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Regulatory Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Regulatory Coordinator Stellenangebote:
- Abb Vie (6 Jobs)
- IQVIA (4 Jobs)
- Trelleborg Antivibration Solutions Germany GmbH (3 Jobs)
- Milestone One (3 Jobs)
In welchen Bundesländern werden die meisten Regulatory Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Regulatory Coordinator Jobs werden derzeit in Bayern (16 Jobs), Hessen (9 Jobs) und Sachsen-Anhalt (9 Jobs) angeboten.
Zu welchem Berufsfeld gehören Regulatory Coordinator Jobs?
Regulatory Coordinator Jobs gehören zum Berufsfeld Regulatory Affairs & Management.