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127 Jobs für Regulatory Affairs Officer


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Job vor 13 Tagen bei Neuvoo.com gefunden Koch- Chemie GmbH

Regulatory Affairs Officer/ Regulatory Compliance Specialist (m/f/x)

• North Rhine- Westphalia Unna ÜBER UNS Koch-Chemie steht seit 1968 für hochwertige Reinigungs- und Pflegeprodukte in den Bereichen Waschchemie, Fahrzeugaufbereitung, Werkstatt und Industrie. Tradition, die sich durch ständige Verbesserungen und Liebe zum Detail auszeichnet: [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Excellence for Experts. In unserer Branche sind wir eines der wenigen Unternehmen, das selbst forscht, p [. .. ]

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Job gestern bei Jobleads gefunden Regulatory Change Lead Private Banking • Genf Führungs-/ Leitungspositionen A global private banking group is seeking a Regulatory Affairs Officer in Geneva to manage regulatory developments and oversee projects within Group Regulatory Affairs. Candidates should have a degree in [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Legal, Finance, or Business, with at least 7 years experience in the field, and fluency in English and either French or German. This role offers a dynamic work environment focused on [. .. ]

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Job am 15.11.2025 bei Jobleads gefunden

Regulatory Affairs Officer

• Genf [. .. ] scale to private and institutional clients. Our sustainable success is based on our talents and on how we partner with our clients and communities to create lasting [...]
MEHR INFOS ZUM STELLENANGEBOT[...] value. Role The Regulatory Affairs Officer is responsible for the monitoring and management of new regulatory developments that might impact the Group. The Officer will also oversee regulatory projects and assist in other activities within Group Regulatory Affairs relevant to regulatory engagement and reporting. Main responsibilities Contribute to and drive the ongoing enhancement of the existing [. .. ]

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Job am 04.11.2025 bei Jobleads gefunden Regulatory Liaisoning Affairs Officer • Hamburg [. .. ] over 2, 200 MW and growing. Solar Development, Engineering, Procurement Construction (EPC) , Operation Maintenance (O M) , Independent Power Producer (IPP) General Information Job Type: Permanent [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Job Purpose: The Regulatory Affairs Officer will be responsible for managing and ensuring compliance with all applicable laws, regulations, policies, and tariff orders governing solar, wind, and hybrid renewable energy projects in India, with a primary focus on Tamil Nadu, Karnataka, and Gujarat. The role involves proactive monitoring of regulatory developments, securing all required licenses and [. .. ]

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Job am 18.10.2025 bei Jobleads gefunden

Regulatory Affairs Officer AMR (w/m/d)

• Hannover, Niedersachsen Abgeschlossenes Studium [. .. ] und Inspektionen. Beobachtung regulatorischer Entwicklungen im Bereich antimikrobieller Resistenzen und translationaler Therapien. Abgeschlossenes Studium im Bereich Pharmazie, Biologie, Chemie, Medizin oder vergleichbarer naturwissenschaftlicher Fachrichtung. Mindestens 3 Jahre [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Berufserfahrung im Bereich Regulatory Affairs, idealerweise im Umfeld von neuartigen Therapien oder Antiinfektiva. Tiefes Verständnis der europäischen und internationalen Regularien für Arzneimittelentwicklung und -zulassung, insbesondere im Bereich innovativer Therapiekonzepte (z. B. personalisierte Arzneimittel, magistrale Rezepturen, ATMPs) . Erfahrung im Umgang mit regulatorischen Plattformen (z. B. CESP, e CTD) . Sicheres Deutsch und Englisch in Wort und [. .. ]

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Job vor 9 Tagen bei Mindmatch.ai gefunden allaboutvienna Healthcare Medical • AT- 9 Wien [. .. ] liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an. . . Permanent Austria-Wien 9 hours [...]
MEHR INFOS ZUM STELLENANGEBOT[...] ago Public Affairs Manager (f/m/d) Job Description Summary #LI-Hybrid Location: Vienna, Austria At Novartis, one of Austrias leading pharmaceutical companies, we are driven by our purpose: to improve and extend peoples lives. We. . . Permanent Dedalus Austria-Wien 9 hours ago Fullstack Developer (m/f/d) Location: Vienna, [. .. ] Austria on market and sales strategy issues along the entire life cycle of a product. This includes market and competition analyses, . . . Permanent Iqvia Austria-Wien 9 hours ago Regulatory Start Up Specialist I, IQVIA Med Tech, Austria Regulatory Start Up Specialist I, IQVIA Med Tech, Austria Join to apply for the Regulatory Start Up Specialist I, IQVIA Med Tech, Austria role at IQVIAJob Overview Perform tasks at a country level. . . Permanent Austria-Wien 9 hours ago Senior [. .. ] strengths, we are redefining healthcare through sustainable action and innovation. For a behind-the-scenes look, check out this. . . Permanent Ifc Austria-Wien 9 hours ago (Associate) Investment Officer (Associate) Investment Officer Job #: req34988 Organization: IFC Sector: Operations Grade: GF Term Duration: 3 years 0 months Recruitment Type: Local Recruitment Location: Vienna, Austr. . . Permanent Austria-Wien 9 hours ago Human Factors Engineer Medical Apps UX Usability A leading global healthcare company in Vienna is seeking [. .. ]

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Job vor 11 Tagen bei Mindmatch.ai gefunden Blueprint Medicines, a Sanofi company

Field Medical Advisor, Alpine (Temporary)

• AT- 9 Wien Homeoffice möglich [. .. ] (s) : Vienna Austria Level of position: Associate Director Position type: 60 field-based 40 home-office based; Temporary Reporting Line: This role reports to the Director of International [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Medical Affairs How will your role help us transform hope into reality The Field Medical Advisor role at Blueprint Medicines Alpine is a critical position within the organization responsible for providing medical scientific and strategic expertise to support Switzerland and Austrias development and commercialization programs. As a Field Medical Advisor you will [. .. ] execution Actively supports upcoming launches by the means of Blueprint Medicines company sponsored symposia and other activities. Reviews and signs off local educational and promotional material as the responsible information officer for the corresponding indication and of clinical trial treatment plans and protocols of Phase IV projects in line with local compliance regulations. Supports interventional and non-Interventional clinical trials in close collaboration with with Clinical development Clinical Operations and Global Medical Affairs teams. Ensures a strategic approach to such programs [. .. ] implementation of launches (pre and post-launch plans) . Solid understanding of the capabilities of the medical affairs function in general the Hematology/ Oncology/ Allergology medical environment as well as Regulatory HTA Early Access Program and RCTs requirements. Ability to maintain scientific credibility through effective scientific communication Superior ability and leadership presence to represent Blueprint Medicines in the medical community as an ambassador. Has confidence and optimism enabling the development of strong relationships internally and externally with executive level leaders. Demonstrates [. .. ]

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Job am 08.11.2025 bei Mindmatch.ai gefunden Osce Associate Project Co-ordination Officer (S) • AT- 9 Wien Associate Project Co-ordination Officer (S) This position is open for secondment only and participating States are kindly reminded that all costs in relation to an assignment at the Secretariat must [...]
MEHR INFOS ZUM STELLENANGEBOT[...] be borne by their authorities. Candidates should, prior to applying, verify with their respective nominating authority to which extent financial remuneration and/or benefit [. .. ] The Programming and Evaluation Support Unit (PESU) assists the Secretary General and the Chairpersonship in the implementation of the Organizations Project Management framework and standards, in line with the Common Regulatory Management System (CRMS) and with the recognized international standards. It is the primary point of contact for the Chairpersonship and participating States delegations on programmatic and project management matters in relation to the Unified Budget (UB) process, as well as the Extrabudgetary contributions. PESU advises senior management and field operations [. .. ] Job Type: Seconded Number of posts: 1 Issue Date: Aug 18, 2025 Employee Status: Fixed Term Schedule: Fulltime Education Level: Masters Degree (Secondlevel university degree or equivalent) Job Field: Political Affairs Target Start Date: As soon as possible J-18808-Ljbffr 68754039 [. .. ]

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Job am 06.11.2025 bei Mindmatch.ai gefunden European Society of Radiology

Junior EU Policy Officer (f/m/x)

• AT- 9 Wien Absolventen, Einsteiger, Trainees [. .. ] field, the European Congress of Radiology (ECR) , in Vienna. Do you want to be at the forefront of Europes healthcare transformation? Join the ESR as a [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Junior EU Policy Officer and shape the future of European healthcare through evidence-based policy. Tasks As Junior EU Policy Officer, you will play a vital role in monitoring legislation, developing evidence-based policy positions, and building bridges between EU institutions and Europes radiology community. Your work as a member of the ESR department of European and International Affairs will include: Actively monitor, analyse and comment EU health and digital policy developments, legislative files, and institutional initiatives impacting medical imaging, cancer care, artificial intelligence, and health data governance Engage directly with radiologists and clinical experts to gather insights, identify challenges, and transform their input into powerful, evidence-informed contributions to EU health policy Develop position papers, regulatory analyses and presentations for the ESR on key topics and issues together in close collaboration with ESR experts and working groups Act as a bridge between EU institutions and the radiology community translating policy developments into clear messages for clinicians, and ensuring their knowledge and on-the-ground experience is [. .. ]

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Job am 25.09.2025 bei Mindmatch.ai gefunden Vienna Insurance Group (VIG) Jurist:in Compliance (Karenzvertretung) • AT- 9 Wien Homeoffice möglich Abgeschlossenes Studium [. .. ] aus datenschutzrechtlichen Gründen keine Bewerbungen per E-Mail entgegennehmen dürfen. Verwenden Sie daher den Link zu unserem Bewerbungsportal. Senior Compliance Spezialist:in für Geldwäscheprävention und Finanzsanktionen (m/w/d) Qualitätssicherungs- und [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Regulatory Affairs Manager:in Content Manager:in-Schwerpunkt Compliance ESG Einstieg in Compliance Forensic Services-Wirtschaftskriminalität im Fokus Expert:in im Bereich Compliance/ Independence (w/m/d) Manager (w/m/d) im Credit Management Team im Bereich Governance, Risk Compliance Advisory IT-Security Compliance Officer (m/w/d) (1 Jahr Befristet-Karenzvertretung) Business Prozess Analystin im Forderungsmanagement Business Analyst-Intranet Platform Inhouse Apps (m/w/x) - Karenzvertretung Business Analyst Prozessmanagement (mensch) - (VZ/ 38, 5 Std. ) J-18808-Ljbffr 63015334 [. .. ]

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Job am 16.11.2025 bei Jobleads gefunden

Legal Counsel Compliance Officer (w/m/d)

• Stuttgart, Baden- Württemberg Beratungs-/ Consultingtätigkeiten Homeoffice möglich Deine Aufgaben Als Legal Counsel Compliance Officer (w/m/d) hältst du Goya Finance rechtlich und regulatorisch auf Kurs. Du arbeitest eng mit dem Management zusammen, koordinierst alle rechtlichen Themen und [...]
MEHR INFOS ZUM STELLENANGEBOT[...] stellst sicher, dass unsere Compliance-Prozesse wirksam, pragmatisch und zukunftsfähig sind. Deine Arbeit schafft Vertrauen intern wie extern. Verantwortung für das Vertragswesen und zentrale Ansprechperson für [. .. ]

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Job am 11.11.2025 bei Jobleads gefunden Legal Counsel Compliance Officer (w/m/d) • Heidelberg, Baden- Württemberg Beratungs-/ Consultingtätigkeiten Homeoffice möglich Deine Aufgaben Als Legal Counsel Compliance Officer (w/m/d) hältst du Goya Finance rechtlich und regulatorisch auf Kurs. Du arbeitest eng mit dem Management zusammen, koordinierst alle rechtlichen Themen und [...]
MEHR INFOS ZUM STELLENANGEBOT[...] stellst sicher, dass unsere Compliance-Prozesse wirksam, pragmatisch und zukunftsfähig sind. Deine Arbeits schafft Vertrauen intern wie extern. Verantwortung für das Vertragswesen und zentrale Ansprechperson für [. .. ]

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Job am 10.11.2025 bei Jobleads gefunden Legal Counsel Compliance Officer (w/m/d) • Stuttgart, Feldberg (Ort) , Baden- Württemberg Stuttgart, Feldberg (Ort) Beratungs-/ Consultingtätigkeiten Homeoffice möglich Permanent employee, Full-time Baden-Württemberg, Remote, Neustadt a. d. Weinstraße, Heidelberg, Rheinland-Pfalz, Stuttgart Deine Aufgaben Als Legal Counsel Compliance Officer (w/m/d) hältst du Goya Finance rechtlich und regulatorisch auf Kurs. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Du arbeitest eng mit dem Management zusammen, koordinierst alle rechtlichen Themen und stellst sicher, dass unsere Compliance-Prozesse wirksam, pragmatisch und zukunftsfähig sind. Deine Arbeit schafft Vertrauen intern wie extern. Verantwortung für das Vertragswesen und zentrale Ansprechperson für [. .. ]

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Job am 05.11.2025 bei Jobleads gefunden Head of Compliance (m/f/x) • München, Bayern Führungs-/ Leitungspositionen Jobticket Job Description Act as Ba Fin-appointed Compliance officer for Ma Comp-and Ma Risk-Compliance and Single Safeguarding Officer Develop, implement, and maintain robust compliance policies, procedures, controls, and frameworks. Regularly [...]
MEHR INFOS ZUM STELLENANGEBOT[...] review and update these to align with regulatory changes and industry best practices. Engage cross-functionally as well as with internal and external auditors to implement a best-in-class compliance management program, in line with regulatory standards and industry best practices Coordinate compliance-related projects with internal teams and external partners. Lead the development and enhancement of [. .. ]

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Job am 17.10.2025 bei Jobleads gefunden

Global Head of Pharmacovigilance

• Stuttgart, Baden- Württemberg Führungs-/ Leitungspositionen [. .. ] strategic leadership role responsible for guiding safety strategy, ensuring compliance, and driving successful trial conduct for company assets across all stages of development. This role directs safety [...]
MEHR INFOS ZUM STELLENANGEBOT[...] strategy, operations, and regulatory compliance for oncology drug products across clinical development and commercialisation phases. This leadership role is central to ensuring safe, compliant, and successful oncology drug development and to maximising patient safety from clinical trials to postmarketing surveillance. This position will report to the Chief Medical Officer and either work on a hybrid basis from the company office in Germany or on a remote basis. Your mission Develop and execute the overall drug safety and pharmacovigilance (PV) strategy aligned with company and global regulatory requirements, especially for oncology assets. Oversee safety surveillance, signal detection, risk assessment, and [. .. ] plans, data exchange agreements, and readiness for health authority inspections. Represent the company in safetyrelated interactions with regulatory agencies, partners, and external stakeholders. Collaborate crossfunctionally with clinical development, regulatory, medical affairs, and other teams integrating safety across the product lifecycle. Ideally, you will have : A medical degree (MD, MBBS, DO) or equivalent clinical degree. 1215+ years experience in drug safety/ pharmacovigilance with at least 5 years at a senior leadership level in biotech and pharma. Oncology experience is required. Experience [. .. ]

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Job am 28.09.2025 bei Jobleads gefunden Global Head of Pharmacovigilance • Düsseldorf, Nordrhein- Westfalen Führungs-/ Leitungspositionen [. .. ] leadership role responsible for guiding safety strategy, ensuring compliance, and driving successful trial conduct for company assets across all stages of development. This role will direct safety [...]
MEHR INFOS ZUM STELLENANGEBOT[...] strategy, operations, and regulatory compliance for oncology drug products across clinical development and commercialisation Phases. This leadership role is central to ensuring safe, compliant, and successful oncology drug development and to maximising patient safety from clinical trials to post-marketing surveillance. This position will report to the Chief Medical Officer and can be based on a hybrid basis from the company office in Germany or remotely. Your mission Develop and execute the overall drug safety and pharmacovigilance (PV) strategy aligned with company and global regulatory requirements, especially for oncology assets. Oversee safety surveillance, signal detection, risk assessment, and risk mitigation [. .. ] exchange agreements, and readiness for health authority inspections. Represent the company in safety-related interactions with regulatory agencies, partners, and external stakeholders. Collaborate cross-functionally with clinical development, regulatory, medical affairs, and other teams, integrating safety across the product lifecycle. Ideally, you will have : A medical degree (MD, MBBS, DO) or equivalent clinical degree. 1215+ years experience in drug safety/ pharmacovigilance with at least 5 years at a senior leadership level in biotech and pharma. Oncology experience is required. Experience [. .. ]

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Job am 27.09.2025 bei Jobleads gefunden

Medical Director Hematology Oncology, Country Medical Director Germany (m/f/d)

• München, Bayern Führungs-/ Leitungspositionen Medical Director Hematology Oncology, Country Medical Director Germany (m/f/d) 1 day ago Be among the first 25 applicants Summary This is a key leadership position in Medical Affairs in [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Germany, Europe. Overview This person will actively participate/ lead a broad range of medical affairs activities in Oncology/ Hematology such as the development of medical strategies for Germany, the preparation support of investigator initiated research (IIR) programs, the management of the German Medical Science Liaisons (MSL) team and the [. .. ] people management experience required with min 2+ years Hematology/ oncology experience required Familiarity with GCP/ ICH/ FDA requirements as well as clinical trial design, biostatistics, medical writing, product safety, and regulatory affairs Strong interpersonal, verbal and written communication skills. Strong public speaking skills Excellent leadership and management skills Ability to influence and work effectively across functions and operate in a matrix environment Ability to travel up to 30 of working time Disclaimer: The above statements are intended to describe the general [. .. ] of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incytes data protection officer, and your supervisory authority (if applicable) . Please contact if you have any questions or concerns or would like to exercise your rights. Seniority level Executive Employment type Full-time Job function Health Care Provider Industries Referrals increase your chances of interviewing at Incyte by 2x Sign in to set [. .. ]

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Neu Job vor 4 Std. bei Jobleads gefunden Quality Manager (m/f/d) Focus: Product approvals and conformity • Bocholt, Nordrhein- Westfalen [. .. ] environment. Does this sound like you? Then this position is your chance to contribute your knowledge and talent to a strong company and help shape the future [...]
MEHR INFOS ZUM STELLENANGEBOT[...] of communication Conformity officer for the Consumer Electronics division Technical responsibility for compliance with legal approval requirements Single point of contact for handling international approvals Preparation of approval documentation (technical construction files) and declarations of conformity (Do Cs) Responsibility for the Gigaset laboratories Environment and telecommunications Commissioning of external laboratories and evaluation of test [. .. ] Fi Alliance What you bring to the table: Degree in engineering, industrial engineering or a comparable field of study desirable Experience in the area of type approvals, product approvals or regulatory affairs High level of technical understanding Experience in quality management and PLM processes Very good analytical skills, strong organisational and communication skills, and ability to work in a team Good written and spoken English That awaits you Able to work from home Further education Responsible for yourself Canteen Accessibility Health insurance [. .. ]

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Neu Job vor 4 Std. bei Jobleads gefunden

IT-Risk Governance Officer (m/w/d) mit Schwerpunkt Governance und Regulatorik

• Stuttgart, Baden- Württemberg Homeoffice möglich Abgeschlossenes Studium Flexible Arbeitszeiten Sabbaticals Referenznummer: 16919-Einsatzort: Stuttgart, Leipzig oder Berlin-Unternehmen : LBBW-Funktionsbereich: Informationstechnologie-Vollzeit/ Teilzeit: 100 Die LBBW zählt zu den führenden Banken Deutschlands und ist ein innovatives Unternehmen im Finanzsektor. Neben traditionellen Bankdienstleistungen beschäftigen [...]
MEHR INFOS ZUM STELLENANGEBOT[...] wir uns mit den Bereichen Digitalisi [. .. ]

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Neu Job vor 4 Std. bei Jobleads gefunden Global Head of Pharmacovigilance • Frankfurt (Oder) , Brandenburg Führungs-/ Leitungspositionen [. .. ] role responsible for guiding safety strategy, ensuring compliance, and driving successful trial conduct for company assets across all stages of development. This be responsible for directing safety [...]
MEHR INFOS ZUM STELLENANGEBOT[...] strategy, operations, and regulatory compliance for oncology drug products across clinical development and commercialisation phases. This leadership role is central to ensuring safe, compliant, and successful oncology drug development and to maximising patient safety from clinical trials to post-marketing surveillance. This position will report to the Chief Medical Officer and either work on a hybrid basis from the company office in Germany or on a remote basis. Your mission Develop and execute the overall drug safety and pharmacovigilance (PV) strategy aligned with company and global regulatory requirements, especially for oncology assets. Oversee safety surveillance, signal detection, risk assessment, and [. .. ] exchange agreements, and readiness for health authority inspections. Represent the company in safety-related interactions with regulatory agencies, partners, and external stakeholders. Collaborate cross-functionally with clinical development, regulatory, medical affairs, and other teams integrating safety across the product lifecycle. Ideally, you will have : A medical degree (MD, MBBS, DO) or equivalent clinical degree. 1215+ years experience in drug safety/ pharmacovigilance with at least 5 years at a senior leadership level in biotech and pharma, Oncology experience is required. Experience [. .. ]

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Job gestern bei Jobleads gefunden Compliance Officer • Herborn, Hessen Für unseren Mandanten, ein international führendes Unternehmen in der Luft- und Raumfahrt sowie Verteidigung, suchen wir engagierte Mitarbeitende für den Standort in Herborn. Weltweit beschäftigt das Unternehmen über 100.000 Kolleg:innen, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] am deutschen Standort sind es rund 800. Seit mehr als 60 Jahren steht unser Mandant für höchste Qualität in de [. .. ]

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Job gestern bei Jobleads gefunden Global Head of Pharmacovigilance Führungs-/ Leitungspositionen [. .. ] leadership role responsible for guiding safety strategy, ensuring compliance, and driving successful trial conduct for company assets across all stages of development. The role will direct safety [...]
MEHR INFOS ZUM STELLENANGEBOT[...] strategy, operations, and regulatory compliance for oncology drug products across clinical development and commercialisation phases. It is central to ensuring safe, compliant, and successful oncology drug development and maximising patient safety from clinical trials to postmarketing surveillance. This position will report to the Chief Medical Officer and may work on a hybrid basis from the company office in Germany or remotely. Your mission Develop and execute the overall drug safety and pharmacovigilance (PV) strategy aligned with company and global regulatory requirements, especially for oncology assets. Oversee safety surveillance, signal detection, risk assessment, and risk mitigation for [. .. ] plans, data exchange agreements, and readiness for health authority inspections. Represent the company in safetyrelated interactions with regulatory agencies, partners, and external stakeholders. Collaborate crossfunctionally with clinical development, regulatory, medical affairs, and other teams integrating safety across the product lifecycle. Ideally, you will have: A medical degree (MD, MBBS, DO) or equivalent clinical degree. 1215+ years experience in drug safety/ pharmacovigilance with at least 5 years at a senior leadership level in biotech and pharma. Oncology experience is required. Experience with [. .. ]

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Job gestern bei Jobleads gefunden Academic Services Leader Compliance Enrolment Führungs-/ Leitungspositionen A prominent academic institution is seeking a Senior Officer for Academic Administration and Compliance. You will lead the Academic Services team, oversee student enrolment, and ensure compliance with academic [...]
MEHR INFOS ZUM STELLENANGEBOT[...] processes. Ideal candidates will have experience in student administration, strong digital skills, and excellent communication abilities. Join us to support students in achieving their academic goals at one of Australias [. .. ]

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Job gestern bei Jobleads gefunden Senior Officer, Academic Administration and Compliance Senior Officer, Academic Administration and Compliance Shape Futures. Inspire Success. Join UQ College. About UQ College UQ College (UQC) is a Registered Training Organisation and proud member of The [...]
MEHR INFOS ZUM STELLENANGEBOT[...] University of Queensland (UQ) community. We provide domestic and international students with access to further and higher education through a diverse range of [. .. ]

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Job vor 2 Tagen bei Jobleads gefunden Senior Compliance Officer (d/f/m) • Düsseldorf, Nordrhein- Westfalen Duesseldorf Senior Compliance Officer (d/f/m) TK Elevator Join to apply for the Senior Compliance Officer (d/f/m) role at TK Elevator. You will foster the TK Elevator ethics and compliance culture [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and awareness in the Business Unit Europe Africa. You will ensure consistent implementation of the global TK Elevator ethics and [. .. ]

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Häufig gestellte Fragen

Wieviel verdient man als Regulatory affairs officer pro Jahr?

Als Regulatory affairs officer verdient man zwischen EUR 55.000,- bis EUR 90.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Regulatory Affairs Officer Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 127 offene Stellenanzeigen für Regulatory Affairs Officer Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Regulatory Affairs Officer Jobs?

Aktuell suchen 10 Unternehmen nach Bewerbern für Regulatory Affairs Officer Jobs.


Welche Unternehmen suchen nach Bewerbern für Regulatory Affairs Officer Stellenangebote?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Regulatory Affairs Officer Stellenangebote:


  • Bio Talent (11 Jobs)
  • Koch- Chemie GmbH (1 Job)
  • allaboutvienna (1 Job)
  • Osce (1 Job)
  • European Society of Radiology (1 Job)


In welchen Bundesländern werden die meisten Regulatory Affairs Officer Jobs angeboten?

Die meisten Stellenanzeigen für Regulatory Affairs Officer Jobs werden derzeit in Bayern (18 Jobs), Nordrhein-Westfalen (16 Jobs) und Baden-Württemberg (13 Jobs) angeboten.


Zu welchem Berufsfeld gehören Regulatory Affairs Officer Jobs?

Regulatory Affairs Officer Jobs gehören zum Berufsfeld Regulatory Affairs & Management.


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