THOR GmbH sucht in eine/n Regulatory Affairs Manager (m/w/d) Fachgruppe Reach & Regulatory Services (ID-Nummer: 13685251)
sebamed sucht in eine/n Regulatory & Safety Affairs Manager (ID-Nummer: 13315250)
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.
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)
Union Investment sucht in eine/n Data Scientist & Regulatory Affairs Manager*in (ID-Nummer: 13764691)
Union Investment sucht in eine/n Data & AI Regulatory Affairs Manager*in (ID-Nummer: 13764690)
AESCULAP AG sucht in eine/n Regulatory Affairs Manager (w/m/d) (ID-Nummer: 13747731)
KEYMKR GmbH sucht in Lübeck eine/n Regulatory Affairs Manager (m/f/d) (ID-Nummer: 13023224)
ulrich GmbH & Co. KG sucht in eine/n Regulatory Affairs Manager (m/w/d) (ID-Nummer: 13686257)
UROMED Kurt Drews KG sucht in eine/n Regulatory Affairs Manager (m/w/d) (ID-Nummer: 13723958)
ZEISS sucht in eine/n Regulatory Affairs Manager Software (m/w/x) (ID-Nummer: 12889644)
ZEISS sucht in eine/n Manager Labeling & Regulatory Projects (f/m/x) (ID-Nummer: 13753083)
Medipac GmbH sucht in eine/n QM/Regulatory Affairs Manager (m/w/d) (ID-Nummer: 13756738)
WISTEMA GmbH sucht in eine/n Quality und Regulatory Affairs Manager (m/w/d) (ID-Nummer: 13752345)
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)
Christeyns GmbH sucht in eine/n Regulatory Affairs Manager (m/w/d) für die Region DACH (ID-Nummer: 13714408)
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.
Denk Pharma GmbH & Co. KG sucht in eine/n Junior Manager (m/w/d) Regulatory Affairs für die Region Afrika (ID-Nummer: 13756438)
Lohmann & Rauscher GmbH & Co. KG sucht in eine/n Regulatory Affairs Manager Clinical & Biological Evaluation (m/w/d) (ID-Nummer: 13715856)
Lohmann & Rauscher GmbH & Co. KG sucht in eine/n Regulatory Affairs Manager Clinical & Biological Evaluation (m/w/d) (ID-Nummer: 13700444)
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.
Vaillant GmbH sucht in eine/n Senior Project Manager (m/w/d) Information Security & Regulatory Compliance (ID-Nummer: 13732172)
Heine Optotechnik GmbH & Co. KG sucht in eine/n Junior Regulatory Affairs Manager mit technischem Verständnis – Medizintechnik (m/w/d) (ID-Nummer: 13673266)
Deutsches Institut für Zell- und Gewebeersatz gGmbH sucht in eine/n Senior Regulatory Affairs Manager* (m/w/d) / Non-profit-Pharmaunternehmen (ID-Nummer: 13676018)
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.
x1F GmbH sucht in eine/n Manager SAP Banking (m/w/d) im Team Finance, Risk and Regulatory Reporting (ID-Nummer: 13752733)
regenold GmbH sucht in eine/n Regulatory Affairs Manager (m/f/d) in-vitro diagnostic medical devices / CDx I 80-100% (ID-Nummer: 13764773)
x1F GmbH sucht in eine/n Senior Manager / Director Cash & Liquidity Management (m/w/d) im Bereich Finance, Risk & Regulatory Reporting (ID-Nummer: 13752753)
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.
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.
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.
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
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.
Joining the team provides the opportunity to work with one single client and to manage clinical research projects in different therapeutic areas. We currently offer the exciting opportunity to join the team as Local Trial Manager (m/w/d) in full-time and work home-based throughout Germany.
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 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 Middle East Africa.
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.
Lead the full sales cycle from first contact to contract signature. Establish and manage international sales channels, partner networks, and key accounts. Conduct negotiations at C-level with OEMs, Tier-1s, and enterprise customers.
We are looking for a skilled Engineering Project Manager (m/f/d) to lead and coordinate technical development projects related to Grid Code Compliance for wind turbines. In this role, you will be responsible for ensuring that our turbine platforms meet the latest regulatory requirements across various global markets.
We are looking for a skilled Engineering Project Manager (m/f/d) to lead and coordinate technical development projects related to Grid Code Compliance for wind turbines. In this role, you will be responsible for ensuring that our turbine platforms meet the latest regulatory requirements across various global markets.
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.
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.
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.