Union Investment sucht in eine/n Data Scientist & Regulatory Affairs Manager*in (ID-Nummer: 13764691)
AESCULAP AG sucht in eine/n Regulatory Affairs Manager (w/m/d) (ID-Nummer: 13747731)
UROMED Kurt Drews KG sucht in eine/n Regulatory Affairs Manager (m/w/d) (ID-Nummer: 13723958)
Dr. Kurt Wolff GmbH & Co. KG sucht in eine/n Manager Regulatory Affairs (m/w/d) (ID-Nummer: 13572382)
THOR GmbH sucht in eine/n Regulatory Affairs Manager (m/w/d) Fachgruppe Reach & Regulatory Services (ID-Nummer: 13685251)
ZEISS sucht in eine/n Regulatory Affairs Manager Software (m/w/x) (ID-Nummer: 12889644)
BEC Medical GmbH sucht in eine/n Innovativer Qualitätsmanager / Regulatory Affairs Manager Medizinprodukte (Mensch) (ID-Nummer: 13669004)
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.
regenold GmbH sucht in eine/n Regulatory Affairs Manager (m/f/d) in-vitro diagnostic medical devices / CDx I 80-100% (ID-Nummer: 13764773)
DRK-Blutspendedienst NSTOB gGmbH sucht in eine/n Wissenschaftlicher Mitarbeiter (m/w/d) Arzneimittelzulassung (Manager (m/w/d) Regulatory Affairs / Apotheker (m/w/d)) (ID-Nummer: 13747759)
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.
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.
Körber Technologies Flavor GmbH sucht in eine/n External Affairs & Engagement Manager (m/w/d) (ID-Nummer: 13583110)
AstraZeneca sucht in eine/n Medical Affairs Manager Oncology (Lung Cancer) (m/w/d) (ID-Nummer: 13722966)
Telefon: 05741 330-128 // E-Mail: bewerbungen@gehwol.de Hier können Sie sich die Stellenanzeige "Public Affairs & Internal Communications Manager (m/w/d)" downloaden.
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.
ZEISS sucht in eine/n Manager Labeling & Regulatory Projects (f/m/x) (ID-Nummer: 13753083)
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.
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?
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.
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.
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.
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.
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
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.
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
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 company Pleasant working atmosphere Support throughout the entire application process Look 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
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.
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.
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.
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.
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.
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.
Main job duties: -To take full leadership, operational and financial responsibility for managing a safe, efficient operational standards and profitable site for the organization and the customer(s), -Take full responsibility for managing and running a safe operation and driving a Safety First Culture with all individuals on site by applying and improving the Safety Standards, -Align Objectives & KPIs applicable to your team and consider how these have an impact on site results, including the required frequency for tracking them, how the results are calculated, ensuring the right ownership of each role in the operation, -Align volume forecast with customer and review monthly resource planning with Operations Manager, developing a work strategy for next month / period, including peaks and valleys' seasons, -Track Site Performance understanding the causes for the gap between them, understanding the financial and customer impact resulted by this gap and address actions with Operations Managers to improve it, -Ensure that Standard Operational Procedures (SOP) and Work Instructions (WI) of operational processes are up to date, available at relevant place for employees and that employees are working according to the standard established, via OMS Confirmation, -Ensure your Shift Managers are properly trained according to their training matrix and enable their training and coaching sessions to enhance their personal development - via training matrix and schedule, -Discuss and approve improvement actions that involve customer requirements and SLA's, additional resources and financial investments with the operations managers, support the team during the implementation of improvement actions, -Promote the continuous improvement culture and sustainability of the program with operations managers and their teams, -Participate in a Monthly Results Meeting with the entire leadership team and employees, presenting the site's results, priorities and promoting engagement within the team, -Control your operational processes (inbound, picking, outbound, etc), fulfilling service level agreeded and deadlines established, -Provide leadership for the site in assessing potential, developing talent and succession planning, lead by example, -Ensure adequate security measures are in place to protect the site premises, including the safety of personnel, DSC assets and of the customer's product, -Maintain processes and required statutory qualifications to ensure compliance with all relevant regulatory and local legal obligations, -Act as the first point of contact for the customer relating to site operation matters and build a good relationship to develop trust and ensure strong engagement, -Conduct regular reviews (e.g. monthly) with customer on operational performance and delivery against the agreed KPIs, -Identify and propose opportunities to grow the business with existing customers, -Support Business Development / Account Management on contractual and commercial issues and customer renewal planning.
Für unsere Neugründung innerhalb der FUTRUE Gruppe suchen wir ab sofort einen Venture Manager – Brain-Computer-Interfaces (w/m/d), der mit uns bis 2030 die führende Generation von Brain-Computer-Interfaces entwickelt und so die Grenzen der Medizin neu definiert.
You will also manage a team of technicians and engineers to deliver exceptional service to clients and ensure adherence to best practices and industry standards.
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.
Together, we’re not just shaping brighter smiles, we’re unlocking the potential of people everywhere, including our own. As Regional EMEA Internal Control System (ICS) Manager, you play a key role in strengthening Straumann Group’s internal control and compliance framework across the EMEA region. Supporting the Head of ICS, you will ensure adherence to corporate compliance standards, foster a culture of integrity, and contribute to effective risk management practices.
Quality Assurance / QA Manager (m/w/d) HIER WERDEN SIE ARBEITEN: Unser Mandant ist ein international tätiger Logistikdienstleister mit Hauptsitz in Belgien mit langjähriger Tradition und familiären Werten.
-Ing., or higher)Solid proven project management and leadership experience in mid-sized, complex CapEx projects within the chemical, biotech, or pharmaceutical industryStrong project management skills, including expertise in contract management, cost control, and stakeholder managementDemonstrated experience in process and infrastructure engineering in chemical, biotech, or pharmaceutical environmentsSolid understanding and practical experience with cGxP requirements as well as qualification and validation processesFluent in German and English, both written and spokenProven leadership capabilities with the ability to guide teams and manage departmental responsibilities A highly motivated team and an open way of communication A very renowned companyGood infrastructurePossibilities to work remoteTips on how to prepare a successful application Ihr Kontakt Referenznummer 865168/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Refund Services Product Manager (gn) - Location Romania Your job at DKV Mobility? As part of a leading European B2B platform for on-the-road payment solutions, you will work in an exciting environment.
-Ing., or higher) Solid proven project management and leadership experience in mid-sized, complex CapEx projects within the chemical, biotech, or pharmaceutical industry Strong project management skills, including expertise in contract management, cost control, and stakeholder management Demonstrated experience in process and infrastructure engineering in chemical, biotech, or pharmaceutical environments Solid understanding and practical experience with cGxP requirements as well as qualification and validation processes Fluent in German and English, both written and spoken Proven leadership capabilities with the ability to guide teams and manage departmental responsibilities A highly motivated team and an open way of communication A very renowned company Good infrastructure Possibilities to work remote Tips on how to prepare a successful application Ihr Kontakt Referenznummer 865168/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
As a Service Product Manager, you shape the global service products of the Nordex Group and support our international organization with clear, robust, and market‑oriented solutions.