sebamed sucht in eine/n Regulatory & Safety Affairs Manager (ID-Nummer: 13315250)
Union Investment sucht in eine/n Data Scientist & Regulatory Affairs Manager*in (ID-Nummer: 13764691)
KEYMKR GmbH sucht in Lübeck eine/n Regulatory Affairs Manager (m/f/d) (ID-Nummer: 13023224)
UROMED Kurt Drews KG sucht in eine/n Regulatory Affairs Manager (m/w/d) (ID-Nummer: 13723958)
WR Group GmbH sucht in eine/n Head of (m/w/d) Regulatory Affairs / Regulatory Affairs Manager in der Gesundheitsbranche (Pharmazeut, Chemiker, Biologe o. ä.) (ID-Nummer: 13666361)
BEC Medical GmbH sucht in eine/n Innovativer Qualitätsmanager / Regulatory Affairs Manager Medizinprodukte (Mensch) (ID-Nummer: 13669004)
Allergopharma GmbH & Co. KG sucht in Reinbek eine/n Regulatory Affairs Manager CMC (m/w/d) (ID-Nummer: 13723465)
Zur Verstärkung unseres Teams der Abteilung Regulatory Affairs suchen wir am Standort Bremen einen (Junior) Regulatory Affairs Manager (m/w/d) in Vollzeit. Die Position ist unbefristet. Deine Aufgaben Erlangung und Aufrechterhaltung von internationalen Produktzulassungen Erarbeitung von Zulassungsstrategien für neue Medizinprodukte nach länderspezifischen Vorgaben Kommunikation und enge Zusammenarbeit mit nationalen und internationalen Zulassungsbehörden Laufende Recherche regulatorischer Neuerung und Änderungen zu landesspezifischen Zulassungsanforderungen Dein Profil Abgeschlossenes naturwissenschaftliches, rechtswissenschaftliches oder technisches Studium Erfahrung im Bereich Regulatory Affairs sowie Kenntnisse relevanter Normen und Gesetze (MDR, ISO 13485) sind von Vorteil Ausgeprägtes Verständnis für regulatorische und rechtliche Rahmenbedingungen Gute Deutsch- und Englischkenntnisse in Wort und Schrift, weitere Sprachkenntnisse wünschenswert Sicherer Umgang mit MS Office Eine selbständige, strukturierte und sorgfältige Arbeitsweise, kombiniert mit einer hohen Lernbereitschaft und sehr guten kommunikativen Fähigkeiten BEGO ist ein Familienunternehmen, bei dem das Miteinander an erster Stelle steht.
Zur Verstärkung unseres Teams der Abteilung Regulatory Affairs suchen wir am Standort Bremen einen Senior Regulatory Affairs Manager (m/w/d) in Vollzeit. Die Position ist unbefristet. Deine Aufgaben Erarbeitung von Zulassungsstrategien und eigenverantwortliche Planung und Betreuung regulatorischer Vorgänge zur Erlangung und Aufrechterhaltung von internationalen Produktzulassungen Termingerechte Erstellung bzw.
Lead, Develop and Empower the Team Provide strong technical leadership, foster professional development and ensure continuous growth and engagement of your team. Manage External Service Providers Effectively manage external service providers acting on behalf of CHEPLAPHARM, ensuring quality, compliance and performance.
Christeyns GmbH sucht in eine/n Regulatory Affairs Manager (m/w/d) für die Region DACH (ID-Nummer: 13714408)
Ascend GmbH sucht in Frankfurt am Main eine/n Regulatory Affairs Manager (m/w/d) - Pharmazeutika (Generika) (ID-Nummer: 13548748)
Lohmann & Rauscher GmbH & Co. KG sucht in eine/n Regulatory Affairs Manager Clinical & Biological Evaluation (m/w/d) (ID-Nummer: 13715856)
Deutsches Institut für Zell- und Gewebeersatz gGmbH sucht in eine/n Senior Regulatory Affairs Manager* (m/w/d) / Non-profit-Pharmaunternehmen (ID-Nummer: 13676018)
regenold GmbH sucht in eine/n Regulatory Affairs Manager (m/f/d) in-vitro diagnostic medical devices / CDx I 80-100% (ID-Nummer: 13764773)
The sales office for the AMEAP region is located in Dubai. For the region Europe & AMEAP we are searching for a Manager Regulatory Affairs & Product Labelling, to be based in The Netherlands or at one of the European locations. YOUR ROLE Responsible for compliance of Dawn Foods products with all relevant food legislation in the European and AMEAP markets; this involves raw materials, recipes, labels and other forms of communication Managing and coaching the teams for both Regulatory Affairs (9 employees) and Product Labelling (6 employees) across the various international locations Embedding the regulatory function as integral part of product management, product development, procurement, production and quality assurance processes; risk assessment of new legislation on manufactured and marketed products Contributing to certification audits in close cooperation with Quality Assurance with respect to product specifications and compliance Ensuring that all product labels are compliant with relevant food legislation in the various countries.
ZEISS sucht in eine/n Manager Labeling & Regulatory Projects (f/m/x) (ID-Nummer: 13753083)
Manager Public Affairs (m/w/d) 1047 Brussels Bruxelles Belgium Marketing & Communications Berufseinsteiger / Berufserfahrene Vollzeit Berufseinsteiger / Berufserfahrene About us The ALDI Nord group is one of the leading food retailers.
Dann könnte diese Stelle Ihr nächster Karriereschritt als Group NATO Affairs Manager (w/m/d) sein! Lesen Sie weiter… Mit Ihrer Erfahrung, Ihrem Know-how und Ihrer Leidenschaft können Sie sich bei den folgenden Themen und Aufgaben bei uns einbringen: Unterstützung des Vice President (w/m/d) EU-/NATO-Strategie & Bilaterale Zusammenarbeit bei der Entwicklung und Steuerung des Konzernansatzes gegenüber der NATO in enger Zusammenarbeit mit den Fachabteilungen und nationalen Stellen Beobachtung der strategischen Entwicklungen der NATO und ihrer Umsetzung in Initiativen und Instrumente Durchführung strategischer Analysen von NATO Initiativen und Instrumenten sowie Bewertung der operativen Auswirkungen und Erarbeitung von Handlungsvorschlägen Verfassung von Dokumentationen, Zusammenfassungen, internen Warnmeldungen und Empfehlungen zu wichtigen Entwicklungen auf NATO-Ebene in den Bereichen Kapazität, Industrie und Standardisierung Beitrag zur Einrichtung, Strukturierung und Moderation von internen Arbeitsgruppen Ansprechperson für strategische Fragen im Zusammenhang mit NATO-Angelegenheiten aus internen Teams Vorbereitung von Referenzdokumenten, Diskussionen und strategischen Notizen für die Meetings des Vice President (w/m/d) EU-/NATO-Strategie & Bilaterale Zusammenarbeit mit externen Stakeholdern Vertretung des Unternehmens in Meetings oder externen Arbeitsgruppen im Auftrag des VP (w/m/d) EU-/NATO-Strategie & Bilaterale Zusammenarbeit Beitrag zur Festlegung sektoraler Positionen, insbesondere im Rahmen der Arbeit von Berufsverbänden mehr weniger WAS SIE DAFÜR MITBRINGEN SOLLTEN Hochschulabschluss z.
Medical Affairs Manager (m/w/d) – Kardiologie – Wohnort bundesweit in Frankfurt am Main Sie arbeiten als Medical Affairs Manager (m/w/d) für ein renommiertes, international stark wachsendes Unternehmen, das als Marktführer in der Medizintechnik etabliert ist.
Manufacturing, Sales, Sourcing and Technical Departments Accountable for ensuring the quality of all locally sourced and manufactured products and for the compliance to food, HACCP and FSSC/ISO standards Developing regulatory strategy in the Europe region and establishing the framework for the provision of strategic advice and recommendations on legislative development in line with business requirements Building and maintaining critical relationships with key decision makers and stakeholders, both internally and externally Taking the lead in responsibility for all quality & food safety issues and ensuring crisis management when necessary Working closely together with Fonterra’s global network, including New Zealand and US Reporting to the Director Supply Chain and FSQR of Fonterra Europe YOUR PROFILE BSc or MSc degree in Food Science & Technology or similar Senior management experience in Quality Assurance, Food Safety and Regulatory Affairs in a comparable international business, preferably in food, feed or pharma Knowledge of various international food safety and quality systems Relevant project management experience, preferably in manufacturing Understanding of EU food regulatory environment Able to deal with and manage complexity, building strong relationships, striving for solutions and results Excellent influencing, stakeholder management and communication skills with fluency in English Comfortable working and travelling (up to 20%) in an international environment; possibility for hybrid working, max. two days/week from home office Personal skills: strategic vision, business acumen, customer focus, entrepreneurial, natural leader, decisiveness and team player FURTHER INFORMATION AND APPLICATION If you are interested in this position , please contact Jakob Jan Verbraak via email jakobjan@dupp.nl or phone+31 6-51820349 /+31 317-468686.
Symrise AG sucht in eine/n Manager Complaint Management (m/w/d) (ID-Nummer: 13669617)
HUMAN Gesellschaft für Biochemica und Diagnostica mbH sucht in Wiesbaden eine/n Post Market Surveillance Manager (m/w/d) - Teilzeit (ID-Nummer: 13723299)
x1F GmbH sucht in eine/n Manager SAP Banking (m/w/d) im Team Finance, Risk and Regulatory Reporting (ID-Nummer: 13752733)
dein profil: Du besitzt ein erfolgreich abgeschlossenes medizinisches oder naturwissenschaftliches Studium? Du hast bereits Erfahrung als Medical Science Liaison Manager im Bereich Onkologie? Du hast bereits Erfahrungen im Auf- und Ausbau medizinisch wissenschaftlicher Kundennetzwerke sammeln können?
Messe München GmbH sucht in eine/n PR-Manager (m/w/d) (ID-Nummer: 13678233)
Denk Pharma GmbH & Co. KG sucht in eine/n (Junior) Manager Labeling (m/w/d) (ID-Nummer: 13665941)
We bring together sector expertise, global scale and local knowledge to design and manage supply chains from raw materials and manufacturing through to the delivery of finished goods and return services. And by seamlessly connecting local operations across the world we are able to deliver the future of global trade.
PUIG Deutschland GmbH sucht in Düsseldorf eine/n Product Development Manager (m/w/d) in Düsseldorf (ID-Nummer: 13664944)
If you would like to contribute to this diverse and ambitious team, we look forward to receiving your application! What makes your day with us special: Develop and Manage Regional Distributor Partnerships Build, maintain and strengthen long-term relationships with regional distributors across Asia Pacific.
If you would like to contribute to this diverse and ambitious team, we look forward to receiving your application! What makes your day with us special: Develop and Manage Regional Distributor Partnerships Build, maintain and strengthen long-term relationships with regional distributors across Western Europe.
If you would like to contribute to this diverse and ambitious team, we look forward to receiving your application! What makes your day with us special: Develop and Manage Regional Distributor Partnerships Build, maintain and strengthen long-term relationships with regional distributors across Middle East Africa.
PharmaSGP Holding SE sucht in Gräfelfing bei München eine/n (Senior) Brand Manager mit Medical Background (w/m/d) (ID-Nummer: 13747877)
medac Gesellschaft für klinische Spezialpräparate mbH sucht in eine/n Global Market Access and HEOR Manager (all genders) (ID-Nummer: 13678111)
The Clinic Operations Manager works in close partnership with the GM to align operational delivery with the clinic’s strategic and commercial objectives. The General Manager (GM) retains full accountability for financial performance, budgeting, commercial strategy, and overall clinic risk.
This involves the patients’ sense of care, control, value and cost in a broad sense. · To manage situations in the nursing/sonography area not covered by standard operating procedures. · To contribute to the holistic approach to patient care that the clinic endeavors to provide
IQVIA CSMS GmbH sucht in Mannheim eine/n Medical Scientific Liaison Manager (m/w/d) bundesweit - verschiedene Indikationen (ID-Nummer: 10574436)
The Deputy Laboratory Manager will support the Laboratory Manager in the delivery of the service and management of the laboratory team. This is a full-time role working 37.5 hours per week - weekend rotation will be required at approximately 1:4 Key Responsibilities: Full range of clinical procedures, including ICSI, vitrification and PGT Communicating with patients about treatment options and results Quality Management, including supporting with audit, document control, non-compliance, quality control/assurance.
The Deputy Laboratory Manager will support the Laboratory Manager in the delivery of the service and management of the laboratory team. This is a full-time role working 37.5 hours per week - weekend rotation will be required at approximately 1:4 Key Responsibilities: Full range of clinical procedures, including ICSI, vitrification and PGT Communicating with patients about treatment options and results Quality Management, including supporting with audit, document control, non-compliance, quality control/assurance.
DIES SIND IHRE AUFGABEN: Büroorganisation sicherstellen, interne Prozesse gestalten: Abläufe und Prozesse im Fachbereich (Terminplanung und -verfolgung, Schriftverkehr, (elektronische) Ablage, Reiseplanung und Besprechungsorganisation planen, bearbeiten, erfassen und laufend bedarfsgerecht optimierenArbeitszeitdaten managen, Bestellprozesse bedienen, Mitarbeiter des Bereichs bei der Reisebuchung und -abrechnung unterstützenKonzernreporting unterstützen:Tätigkeiten der Abteilung eigenverantwortlich unter Reporting-Gesichtspunkten fortlaufend inhaltlich einordnen und aufbereiten, um regelmäßig verschiedene Konzernberichtsformate (insb.
To learn more please visit http://www.convatecgroup.com The Global Health Economics & Outcome Research Manager (HEOR) will be part of our Market Access and Reimbursement Centre of Excellence (COE) and report into the Director, Global Health Economics and Outcomes Research.
Synformulas GmbH sucht in Gräfelfing eine/n Senior Einkäufer Neuprodukte*| strategischer Einkauf | Sourcing | Lieferantenmanagement | Verhandlung | Healthcare Pharma | Beschaffung | Supply Management | Procurement Manager| München (ID-Nummer: 13650354)
Identification and implementation of timeline optimizations and escalation of important topics to leadership. Manage Key External Stakeholders The Integration Project Manager is ultimately accountable for ensuring external stakeholders Divestment Partner, Contarct Manufacturing Organizations, Sales and Distribution Partners are effectively managed and aligned with integration objectives.
Successful studies in Engineering, Business Administration or Life Sciences (MS/MBA/BS/BA or equivalent) Solid experience in managing major capital projects in the pharmaceutical industry Functional knowledge of cGMPs and manufacturing operations in FDA regulated facility Excellent understanding of project management principles and project lifecycle phases, including knowledge of Validation, CMC and facility regulatory submission requirements Experience to manage high level project budgets Ability to handle many tasks simultaneously and integrate project planning efforts across functions Ability to understand the big picture and approach problem solving in a proactive team manner German knowledge is mandatory Varied work in a renowned companyPleasant working atmosphereSupport throughout the entire application processLook forward to working in an international environment Ihr Kontakt Ansprechpartner Sandro Frei Referenznummer 865163/1 Kontakt aufnehmen E-Mail: sandro.frei@hays.ch Anstellungsart Freiberuflich für ein Projekt
Ensure high-quality, data-driven deliverables that meet the highest standards of medical, ethical, and scientific integrity and conduct. Propose strategies to manage and accelerate timelines for drug development strategies. Identify, promote, and develop innovation in pharmaceutical product development.
Unser Vertrieb arbeitet nah am Markt, lösungsorientiert und partnerschaftlich – mit dem klaren Ziel, nachhaltiges Wachstum für unsere Kunden und für Wentronic zu erzielen. Als Account Manager / Sales Manager* verantwortest du dein Geschäft eigenständig: Du entwickelst Kundenbeziehungen, gewinnst neue Partner und sorgst dafür, dass aus Kontakten belastbare Umsätze werden.
We are seeking an experienced Project Manager / Construction Manager to oversee the delivery of our turnkey timber frame housing projects across the United Kingdom, primarily in the Greater London and Cambridge areas, as well as the Channel Islands.
YOUR PROFILE BSc or MSc degree in Food Science & Technology or similar Senior management experience in Quality Assurance, Food Safety and Regulatory Affairs in a comparable international business, preferably in food, feed or pharma Knowledge of various international food safety and quality systems Relevant project management experience, preferably in manufacturing Understanding of EU food regulatory environment Able to deal with and manage complexity, building strong relationships, striving for solutions and results Excellent influencing, stakeholder management and communication skills with fluency in English Comfortable working and travelling (up to 20%) in an international environment; possibility for hybrid working, max. two days/week from home office Personal skills: strategic vision, business acumen, customer focus, entrepreneurial, natural leader, decisiveness and team player FURTHER INFORMATION AND APPLICATION If you are interested in this position, please contact Jakob Jan Verbraak via email info@dupp.nl or phone +31 317-468686 /+31 6-51820349 .
Job Overview: As an Associate Director, Biostatistics, with regional/site presence, you will manage a team of Biostatistics staff and fulfil the role of site head or functional head within a site. You will provide direction and guidance in carrying out project assignments, interfacing with clients and other internal departments, and applying advanced statistical methods to project work.
We currently offer the exciting opportunity to join the team as Clinical Trial Manager (m/w/d) in full-time and work home-based throughout Germany. In this role you will be accountable for the operational management of the component of clinical trials.