Drug Regulation Stellenangebote


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23 Jobs für Drug Regulation


Stellenangebote Drug Regulation Jobs


Job am 24.03.2026 bei Mindmatch.ai gefunden United Nations

Drug Control Officer (Drug Control Technologies-GRIDS Programme) , Vienna, Austria

• AT- 9 Wien [. .. ] national bodies through automated collection, compilation, analysis, visualization, and exchanges involving drugs, new psychoactive substances (NPS) and related chemicals using machine learning algorithms; Coordinate, maintain, refine and [...]
MEHR INFOS ZUM STELLENANGEBOT[...] operationalize INCB proprietary drug control reporting technologies under the GRIDS Programme (Project Ion Incident Communication System IONICS) , GRIDS Intelligence, Scanning Novel Opioids Online Platforms (SNOOP) , etc) with internal stakeholders, relevant national, regional and international stakeholders and relevant private sector partners, to ensure flow of information; Support the development, management, use and promotion [. .. ] staff members are subject to the authority of the Secretary-General, who may assign them to any of the activities or offices of the United Nations in accordance with staff regulation 1.2 (c) . Further, staff members in the Professional and higher category up to and including the D-2 level and the Field Service category are normally required to move periodically to discharge functions in different duty stations under conditions established in ST/ AI/ 2023/ 3 on Mobility, as [. .. ]

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Job am 18.03.2026 bei Mindmatch.ai gefunden Glenmark Europe Country Manager-Austria • AT- 9 Wien [. .. ] Director and Trade Law Manager Duties: Ensure the proper representation of the company under commercial and trade law aspects. Trade Law: Immediately inform the Pharmacovigilance Department about [...]
MEHR INFOS ZUM STELLENANGEBOT[...] any incident concerning drug safety. Immediately inform the Quality Management Representative about any incidences concerning the Quality Management System, deviations and customer complaints. Ensure compliance with all current versions of relevant laws and regulations in all activities, particularly Austrian Medicinal Product Act/ Arzneimittelgesetz Austrian Regulation on Medicinal Production Sites/ Arzneimittelbetriebsordnung, Trade Law/Gewerberecht. Advise the Managing Directors and all employees in case of any legal changes. Ensure availability for all issues related to medicinal products of the company and in critical situations. Adhere to regulatory restrictions. Ensure that a Quality Management System is established, maintained [. .. ]

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Neu Job vor 4 Std. bei Jobleads gefunden

German Airways Cabin Crew Member Experienced (m/f/d)

• Köln, Nordrhein- Westfalen Koeln [. .. ] A valid EASA Cabin Crew Attestation and at least two years of proven professional experience as a flight attendant. A current medical certificate confirming fitness to fly [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and a negative drug screening result. Instruction per 42 of the German Infection Protection Act and a valid background check (ZÜP) . Minimum age of 20 and a minimum height of 1.60 meters. Business-fluent English is essential; proficiency in German or other languages is a strong asset. The ability to reach your [. .. ] PC with solid IT proficiency. A passport with unlimited validity. For non EU citizens, a valid German residence and work permit are required. A valid hygiene training certificate according to EU Regulation 852/ 2004. Why Choose German Airways? We believe in rewarding our teams expertise with stability, support, and clear opportunities for growth. When you join our family, you receive more than just a jobyou build a career with a respected industry player. What We Offer You? A permanent employment contract with [. .. ]

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Job gestern bei Jobleads gefunden Senior Director, Qualified Person for Pharmacovigilance, Europe Führungs-/ Leitungspositionen [. .. ] Compliance EU QPPV Duties (as per GVP) Act as the legally designated QPPV for the MAH in the EU and other regions as applicable. Ensure compliance with [...]
MEHR INFOS ZUM STELLENANGEBOT[...] EU PV legislation (Regulation (EC) No. 726/ 2004; Directive 2001/ 83/ EC; Commission Implementing Regulation (EU) No 520/ 2012; EMA GVP Modules) and applicable national requirements. Together with GPS leadership, establish and maintain the MAHs global PV System and promote, maintain, and improve compliance with applicable legal PV requirements. Ensure that the MAHs PSMF [. .. ] or senior PV leadership role. Indepth knowledge of GVP, EU PV legislation and global regulatory frameworks. Proven experience managing global PV systems and interacting with health authorities. Excellent understanding of drug development and lifecycle management of medicinal products. Fluent in written and spoken English; fluency in a second European language is an advantage. Preferred Skills Regulatory expertise and strategic thinking. Strong leadership, communication, and organizational skills. Track Record of leading and building a highperforming team. Ability to manage complex global PV [. .. ]

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Job gestern bei Jobleads gefunden

VP Global Pharmacovigilance

[. .. ] cancer that drives our mission and everything that we do on behalf of patients with cancer. Position Summary: Reporting to the CMO, the VP Global Pharmacovigilance has [...]
MEHR INFOS ZUM STELLENANGEBOT[...] overall responsibility for drug safety activities for early and late phase assets, including furthering the development and implementation of the clinical development strategy. The VP will be accountable for overseeing safety and pharmacovigilance across development and expected global launches and, ultimately, postmarket products. The VP must possess a strong knowledge of global pharmacovigilance regulations, [. .. ] condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military and veteran status or any other basis protected by federal, state or local law or ordinance or regulation. #J-18808-Ljbffr 88987359 [. .. ]

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Job gestern bei Jobleads gefunden Principal Transmission Ops NERC Compliance Specialist [. .. ] business regulations Data visualization and presentation skills Experience working in the electric utility industry Additional Information Some positions at PSEG require access to information covered by the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Department of Energys regulation 10 CFR 810 (Part 810) . If applicable, the successful applicant must prove they are: (1) a citizen or national of the USA; OR (2) a lawful permanent resident of the United States (Non-Conditional Permanent I-551/ Green Card/Permanent Resident Card holder) ; OR (3) a citizen, national, [. .. ] citizen, national, permanent resident of any country not listed; OR (4) a Protected Individual under the Immigration and Naturalization Act (8 U. S. C 1324b (a) (3) ) . PSEGLIs drug and alcohol testing program includes pre-employment testing, testing for cause, and post-incident/ accident testing. Employees in federally regulated roles are subject to random testing, including for marijuana. PSEGLI is an equal opportunity employer, dedicated to a policy of non-discrimination in employment, including the hiring process, based on [. .. ]

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Job vor 3 Tagen bei Jobleads gefunden

Design Quality Engineer II

• Aachen, Nordrhein- Westfalen [. .. ] up on actions. Ensure compliance of QMS through authoring and updating Standard Operating Procedures (SOP) . Job Qualifications Must have in depth knowledge of and ability to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] apply quality system regulation, including QSR, ISO 13485, MDSAP and MDd/MDR. Working knowledge and practical application of 21 CFR Part 820, ISO 13485, and ISO 14971 is required. A minimum of a Bachelors degree in an engineering or scientific discipline is required. An advanced degree in a related field is also an asset. [. .. ] reassignment, non-job related mental or physical disability, genetic information, veteran status, military service, application for military service, or membership in any other category protected under law. Abiomed maintains a drug-free workplace. The anticipated annual base pay range for this position is 62, 500-97, 865 Euro. Required Skills Agility Jumps Business Behavior Coaching Compliance Management Continuous Improvement Database Backup Data Savvy Disruptive Innovations Issue Escalation Problem Solving Process Oriented Product Improvements Quality Control (QC) Quality Management Systems (QMS) Quality [. .. ]

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Job vor 3 Tagen bei Jobleads gefunden Configuration Management Engineer [. .. ] Ability to create both technical and nontechnical enduser documentation. Detail-oriented with strong analytical and problemsolving skills. Strong interpersonal skills and ability to work effectively with clients, leadership, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and staff. Regulation 10 CFR 810 compliance required. Desired Qualities Experience with automation, scripting, and orchestration (Ansible, Python, Power Shell, Terraform) . Knowledge of ITSM systems (Service Now) , CMDBs, databases, and related platforms. Experience with endpoint management tools (Big Fix, SCCM, Intune, Solar Winds) . Familiarity with security best practices, regulatory requirements, and industry frameworks (NIST, ISO, CIS) . Drug and Alcohol Testing All roles include preemployment testing, testing for cause, and postincident/ accident testing. Employees in federally regulated roles are subject to random testing, including for marijuana. Use of CBD products may result in a positive test for THC and is not a legitimate medical explanation. EEO Statement PSEGLI [. .. ]

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Job vor 3 Tagen bei Jobleads gefunden Design Quality Engineer II • Aachen, Nordrhein- Westfalen [. .. ] up on actions. Ensure compliance of QMS through authoring and updating Standard Operating Procedures (SOP) . Job Qualifications Must have in depth knowledge of and ability to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] apply quality system regulation, including QSR, ISO 13485, MDSAP and MDd/MDR. Working knowledge and practical application of 21 CFR Part 820, ISO 13485, and ISO 14971 is required. A minimum of a Bachelors degree in an engineering or scientific discipline is required. An advanced degree in a related field is also an asset. [. .. ] reassignment, non-job related mental or physical disability, genetic information, veteran status, military service, application for military service, or membership in any other category protected under law. Abiomed maintains a drug-free workplace. The anticipated annual base pay range for this position is 62, 500-97, 865 Euro. Required Skills Preferred Skills: Agility Jumps, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Database Backup, Data Savvy, Disruptive Innovations, Issue Escalation, Problem Solving, Process Oriented, Product Improvements, Quality Control (QC) , Quality Management [. .. ]

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Job vor 12 Tagen bei Jobleads gefunden PhD position in cell biology • München, Bayern [. .. ] protein biogenesis. THE PROJECT Membrane proteins make up one third of the human proteome. They are critical for any cellular function from movement to immune defense. Membrane [...]
MEHR INFOS ZUM STELLENANGEBOT[...] proteins are major drug targets and their mutations cause numerous severe human diseases. Despite these key roles in biology and medicine, cellular mechanisms of membrane protein biogenesis and control remain ill-defined. The project will investigate biological functions and molecular mechanisms of endoplasmic reticulum membrane protein chaperones in membrane protein biogenesis and quality control. [. .. ] von personenbezogenen Daten im Rahmen Ihrer Bewerbung. (Data protection information on collecting and processing personal data contained in your application in accordance with Art. 13 of the General Data Protection Regulation (GDPR) ) . By submitting your application, you confirm that you have acknowledged the above data protection information of TUM. Kontakt: #J-18808-Ljbffr 86996083 [. .. ]

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Job am 24.03.2026 bei Jobleads gefunden

Director (Regulation and Prequalification of Medicines and Health Products)

• Genf Führungs-/ Leitungspositionen Work-Life-Balance OBJECTIVES OF THE PROGRAMME The objectives of the Department of Regulation and Prequalification of Medicines and Health Products (RPQ) are to ensure the quality, safety and efficacy of medicines [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and health products globally. The immediate strategic objective and priorities is to achieve greater country impact through building capacity of Regulatory systems in LIMC, establishment of reliance mechanism among National Regulatory Authorities, [. .. ] of public health/ disease control programmes. Rich expertise and deep knowledge on the regulatory framework of medicines and health products, i. e. European Medicines Agency (EMA) , US Food and Drug Administration (USFDA) and other Stringent Regulatory Authorities. Extensive expertise in developing and implementing regulatory policies and strategies for medicines and health products, including greenfriendly products. Proven ability to engage and collaborate with diverse stakeholders, i. e. EMA, USFDA, AMA, UNICEF, UNFPA, etc. , to achieve common goals. Strong proficiency in [. .. ]

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Job am 18.03.2026 bei Jobleads gefunden Country Manager-Austria • Wien [. .. ] Director and Trade Law Manager Duties: Ensure the proper representation of the company under commercial and trade law aspects. Trade Law: Immediately inform the Pharmacovigilance Department about [...]
MEHR INFOS ZUM STELLENANGEBOT[...] any incident concerning drug safety. Immediately inform the Quality Management Representative about any incidences concerning the Quality Management System, deviations and customer complaints. Ensure compliance with all current versions of relevant laws and regulations in all activities, particularly Austrian Medicinal Product Act/ Arzneimittelgesetz Austrian Regulation on Medicinal Production Sites/ Arzneimittelbetriebsordnung, Trade Law/Gewerberecht. Advise the Managing Directors and all employees in case of any legal changes. Ensure availability for all issues related to medicinal products of the company and in critical situations. Adhere to regulatory restrictions. Ensure that a Quality Management System is established, maintained [. .. ]

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Job am 07.03.2026 bei Jobleads gefunden

LBd/Learning Behavior Disorders Teacher-Grades K-12

• Unterseen, Bern [. .. ] employment, all employees, including substitute employees, shall pass a medical examination as indicated in 702 KAR 001:160. The medical examination shall be reported on the form required [...]
MEHR INFOS ZUM STELLENANGEBOT[...] by Kentucky Administrative Regulation available at the Board of Education office. The examination shall be provided by a licensed physician, physician assistant (PA) , or Advanced Practice Registered Nurse. Each medical examination shall include a risk assessment for tuberculosis as required by Kentucky Administrative Regulation. Individuals identified by that assessment as being at high [. .. ] test as required by 702 KAR 001:160. A medical exam performed within a ninety (90) - day period prior to initial employment will be accepted. Based on the Board-approved Drug Free/ Alcohol Free School policy 03.23251, all applicants being considered for employment shall be required to submit to a urinalysis test for the detection of illegal use of drugs and alcohol, as part of the required post-offer, pre-employment physical. As a condition of employment, applicants are subject [. .. ]

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Job vor 4 Tagen bei Neuvoo gefunden Rheinische Friedrich- Wilhelms- Universität Bonn W1 tenure track W2-Professur (Juniorprofessur) für Energiehomöostase • Bonn, North Rhine- Westphalia Absolventen, Einsteiger, Trainees Abgeschlossene Ausbildung [. .. ] Bonn ist eine W1 tenure track W2-Professur (Juniorprofessur) für Energiehomöostase zum nächstmöglichen Zeitpunkt zu besetzen. Der/ Die Stelleninhaberin soll den Forschungsbereich Energiehomöostase vertreten und die Forschung zu [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Metabolismus, Fettgewebe-Regulation und Pharmakologische Intervention bei Stoffwechselerkrankungen an der Medizinischen Fakultät der Universität Bonn verstärken. Er/ Sie wird sich in die nachhaltige Weiterentwicklung bestehender Verbundprojekte und Strukturen in diesem Bereich, insbesondere im DFG-geförderten SFB/ TRR333 Brown and Beige Fat Organ Crosstalk, Signaling and Energetics (BA Tenergy) , einbringen. Es wird von [. .. ] single-cell RNA sequencing. Erfahrungen zu spatial omics Technologien sind zusätzlich erwünscht. Erwartet wird eine international sichtbare Forschungsleistung. Darüber hinaus ist das Engagement im Graduiertenausbildungsprogramm Bonn International Graduate School of Drug Sciences (BIGS Drug S) und anderen Verbünden der Medizinischen Fakultät (z. B. im integrativen Adipositas und Stoffwechselforschungszentrum (Bi OM) , im kardiovaskulären Schwerpunkt der Fakultät, SFB1454, und Cluster Immunosensation) erwünscht. Einstellungsvoraussetzungen sind ein abgeschlossenes medizinisches oder naturwissenschaftliches Hochschulstudium sowie die Habilitation oder der Nachweis gleichwertiger wissenschaftlicher Leistungen. Wünschenswert ist Erfahrung in der [. .. ]

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Job vor 11 Tagen bei Neuvoo gefunden aks Aktuelle Krankenpflege Systeme GmbH

Werkstudent Medizintechnik (m/w/d)

• Troisdorf, North Rhine- Westphalia Werkstudenten [. .. ] wie z. B. neue klinische Studien, die sich mit äquivalenten Produkten befassen Sie prüfen regelmäßig die Datenbanken des Bf Ar M (Bundesinstitut für Arzneimittel und Medizinprodukte) sowie [...]
MEHR INFOS ZUM STELLENANGEBOT[...] der FDA (Food and Drug Administration) hinsichtlich Vorkommnissen mit vergleichbaren Produkten und leiten Risiken für unsere Produkte daraus ab Sie sind an Produktprüfungen beteiligt und führen Messungen durch (z. B. Druck-oder Lautstärkemessungen) Sie arbeiten nach Einarbeitung selbstständig und berichten an die Abteilungsleitung Sie beteiligen sich, neben eigenständigen Routineaufgaben, an weiteren Aufgaben aus der Technischen [. .. ] B. dem Risikomanagementprozess sowie der Erstellung von Gebrauchsanweisungen oder der Produktkennzeichnung Sie arbeiten sich schrittweise in die Anforderungen aus der neuen EU-Verordnung 2017/ 745 über Medizinprodukte (MDR Medical Device Regulation) ein und sammeln damit wichtige Kenntnisse für Ihren späteren Berufsalltag Unsere Anforderungen: Angefangenes Studium im Bereich Medizintechnik oder Vergleichbar ab dem 1. Semester Analytische, strukturierte und pragmatische Arbeitsweise Nach einer Einarbeitungsphase arbeiten Sie gerne eigenständig Der Umgang mit Office-Anwendungen und KI-Chatbots ist Ihnen vertraut Sehr gute Deutsch- und [. .. ]

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Job am 18.02.2026 bei Neuvoo gefunden NVision Imaging Technologies Regulatory Affairs Manager-Product Safety Certifications (m/f/d) [. .. ] R D to design safety into the product from day one. Key Responsibilities: European Regulatory Leadership: Maintain and update the Technical File for CE marking under the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Machinery Directive and Regulation (2006/ 42/ EC, 2023/ 1230/ EU) , Pressure Equipment Directive (PED) , and Low Voltage Directive (LVD) , as well as other applicable regulations North American Compliance (US Canada) : Lead the certification process with Nationally Recognized Testing Laboratories (NRTL) to ensure compliance with OSHA safety standards and the National [. .. ] a unique approach-leveraging organic molecules to change lives for the better. Our platform spans from quantum signal enhancement that enables metabolic imaging today to quantum computing that could transform drug discovery tomorrow. Headquartered in Ulm, Germany, and backed by leading investors from the United States and Europe, we are now entering a phase of global commercialization and expansion. With our POLARIS product line, we are extending the capabilities of standard MRIs to enable real-time metabolic imaging, transforming how diseases [. .. ]

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Job am 17.02.2026 bei Neuvoo gefunden Technical University of Munich

Wissenschaftliches Personal, Doktorandenstelle (TV-L E13, 75)

• Munich, Bavaria [. .. ] Munich (TUM) , and Prof. Angela M. Gronenborn, TUM-IAS Hans-Fischer Senior Fellow and University of Pittsburgh. This interdisciplinary research aims to advance protein and RNA structural biology [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and drug interactions by developing and applying innovative F NMR methodologies to study biomolecular structure, dynamics, and interactions in complex environments and live mammalian cells. By combining ultra-high-field NMR with complementary biochemical, computational, and cellular approaches, the project will overcome current limitations in sensitivity and contrast, enabling unprecedented insights into [. .. ] von personenbezogenen Daten im Rahmen Ihrer Bewerbung. (data protection information on collecting and processing personal data contained in your application in accordance with Art. 13 of the General Data Protection Regulation (GDPR) ) . By submitting your application, you confirm that you have acknowledged the above data protection information of TUM. 80963576 [. .. ]

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Job am 21.01.2026 bei Neuvoo gefunden Technical University of Munich NanoLPC: Technik der lichtinduzierten Phasenänderung für neue Prozesse im Nanomaßstab • Munich, Bavaria [. .. ] induced vaporization and the formation of keyhole pores, i. e. , porosity defects, are currently a major limiting factor for metal printing. In nanomedicine, various nanoparticles are [...]
MEHR INFOS ZUM STELLENANGEBOT[...] used for controlled drug delivery and therapies, and laser-excited nanobubble-inducing shockwave is a powerful tool for ablating vitreous opacities in vivo. In solar energy utilization, direct steam generation/ vapor production from bulk or surface fluid surface is a promising technology for enhancing solar energy efficiency in the post-fossil fuel era and [. .. ] von personenbezogenen Daten im Rahmen Ihrer Bewerbung. (data protection information on collecting and processing personal data contained in your application in accordance with Art. 13 of the General Data Protection Regulation (GDPR) ) . By submitting your application, you confirm that you have acknowledged the above data protection information of TUM. 77002425 [. .. ]

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Job am 11.12.2025 bei Neuvoo gefunden Löwenstein Medical Technology GmbH + Co. KG

Project Manager Quality Regulatory FDA Compliance (m/w/d) , Project Manager Quality Regulatory FDA Compliance (m/w/d) bei Löwenstein Medical Technology GmbH + Co. KG softgarden

• Hamburg Homeoffice möglich Flexible Arbeitszeiten Betriebliche Altersvorsorge Jobticket 30+ Urlaubstage Tarifvertrag [. .. ] Ingenieurwesen, Naturwissenschaften oder einer vergleichbaren Fachrichtung Mehrjährige Berufserfahrung in den Bereichen Qualitätsmanagement und Regulatory Affairs innerhalb der Medizintechnik Sicherer Umgang mit regulatorischen Anforderungen an Medizinprodukten, z. B. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] MDR (Medical Device Regulation) und FDA (Food Drug Administration/ 21 CFR Part 11, QSR) Know-how im Projektmanagement zur strukturierten Koordination von Aufgaben, Stakeholdern und Projektzielen Hohe Kommunikationsstärke, analytisches Denken und strukturierte Arbeitsweise Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift Das können Sie von uns erwarten Flexible Arbeitszeiten (Gleitzeit) , unbefristete Anstellung Homeoffice gemäß aktueller Betriebsvereinbarung [. .. ]

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Job am 27.11.2025 bei Neuvoo gefunden Constellis Guard/ESS Operator • Wiesbaden, Hesse [. .. ] nation (Germany) laws Must have a Top-Secret Security Clearance with SCI and CI-Poly based on a SSBI Ability to pass all medical and physical requirements outlined in [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Army Regulation (AR) 190-56 Meet all standards of the IRP as required by AR 190-56 Must be able to speak, read, understand, and write English Must successfully complete all US Government and contractor provided training Must pass initial and recurring scheduled and/or unscheduled drug tests in accordance with (IAW) AR 190-56 Strong administrative knowledge including Outlook, Microsoft Office applications, Share Point, database, and reports management PHYSICAL FITNESS Physically capable of performing assigned guard duties as defined by guard orders Successful completion of a physical fitness test, including 1-mile run in under ten [. .. ]

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Job vor 11 Tagen bei Jooble gefunden IQVIA Senior Clinical Data Team Lead (Senior DTL) - FSP • Regierungsbezirk Darmstadt; Hessen Frankfurt am Main, DE Führungs-/ Leitungspositionen The Sr. CDM will lead and contribute to data management activities in support of Client s studies across all stages of clinical drug development. Summary of Key Responsibilities Contribute [...]
MEHR INFOS ZUM STELLENANGEBOT[...] to data management activities as a lead study data manager in support of Client s clinical studies Lead database build activities including leading cross-functional review of e CRF content, review of edit check specifications, and perform user acceptance testing Monitor data collection, coding, and [. .. ] Contribute to development and implementation of department workflows and infrastructure strategy (such as preferred provider interactions, SOPs, and templates) that reflects data collection standards, consistent with industry best practice and regulation Represent data management and effectively communicate requirements, strategy, timelines and deliverables at internal cross-functional team meetings and meetings with external vendors Participate in the training of external vendors and site staff Participate in the drafting and/or review of timelines consistent with company goals and ensure all deliverables and [. .. ]

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Job vor 11 Tagen bei Jooble gefunden Thomson Reuters Senior Specialist Legal Editor, Practical Law EU Regulatory • Berlin Berlin, DE Work-Life-Balance [. .. ] English and have: At least 5 years post-qualification experience working as a regulatory lawyer in the EU (preferably (but not essential) with expertise of working in capital [...]
MEHR INFOS ZUM STELLENANGEBOT[...] markets/ financial regulation in France or Germany) . Substantial experience of EU regulation law and practice. Excellent writing and communication skills in English, and a passion for writing about legal practice accurately, concisely and in plain English. A collaborative mindset with the ability to work effectively independently and in teams. Strong technical skills [. .. ] orientation, disability, age, marital status, citizen status, veteran status, or any other protected classification under applicable law. Thomson Reuters is proud to be an Equal Employment Opportunity Employer providing a drug-free workplace. We also make reasonable accommodations for qualified individuals with disabilities and for sincerely held religious beliefs in accordance with applicable law. More information on requesting an accommodation here. Learn more on how to protect yourself from fraudulent job postings here. More information about Thomson Reuters can be found [. .. ]

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Job vor 11 Tagen bei Jooble gefunden Military Treatment Facilities under DHA Medical Instrument Technician (Cardiovascular) • Landkreis Kaiserslautern; Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Landstuhl, DE [. .. ] Return Rights. Visit This position may require you to be on-call on a rotational basis, responding to emergency calls at times beyond the normal duty day. This [...]
MEHR INFOS ZUM STELLENANGEBOT[...] is a drug testing designated position (TDP) subject to pre-employment drug test and random drug testing. Incumbent must have and maintain certifications in BCLS and ACLS at all times. Must be able to lift up to 45 lbs. This position requires the completion of a pre-employment Physical Examination and an annual [. .. ] area. If an employee brings a child to an overseas location and that child is entitled to attend a Do D school on a space-required basis in accordance with Do DEA Regulation 1342.13, the Do DEA and the Military Department responsible for providing related services will ensure that the child, if eligible for special education, receives a free appropriate public education, including related services pursuant to Do DI 1342.12 and Do DM 1342.12. If an employee brings an infant or toddler (up [. .. ]

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Häufig gestellte Fragen

Wieviele offene Stellenangebote gibt es für Drug Regulation Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 23 offene Stellenanzeigen für Drug Regulation Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Drug Regulation Jobs?

Aktuell suchen 12 Unternehmen nach Bewerbern für Drug Regulation Jobs.


Welche Unternehmen suchen nach Bewerbern für Drug Regulation Stellenangebote?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Drug Regulation Stellenangebote:


  • Technical University of Munich (2 Jobs)
  • United Nations (1 Job)
  • Glenmark Europe (1 Job)
  • aks Aktuelle Krankenpflege Systeme GmbH (1 Job)
  • NVision Imaging Technologies (1 Job)


In welchen Bundesländern werden die meisten Drug Regulation Jobs angeboten?

Die meisten Stellenanzeigen für Drug Regulation Jobs werden derzeit in Nordrhein-Westfalen (5 Jobs), Hessen (2 Jobs) und Niedersachsen (1 Jobs) angeboten.


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